General Information of the m6A Regulator (ID: REG00006)
Regulator Name Methyltransferase-like 14 (METTL14)
Synonyms
N6-adenosine-methyltransferase non-catalytic subunit; hMETTL14; KIAA1627
    Click to Show/Hide
Gene Name METTL14
Regulator Type WRITER ERASER READER
Regulator Link Click to View Full Information of This Regulator
Full List of Target Gene(s) of This m6A Regulator and Corresponding Potential Drug Response(s)
Apoptosis regulator Bcl-2 (BCL-2)
MCI-186 [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for MCI-186. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MCI-186 through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [2]
Venetoclax [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for Venetoclax. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Venetoclax through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [3]
ABT-263 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for ABT-263. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ABT-263 through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [4]
Oblimersen [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for Oblimersen. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Oblimersen through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [5]
RG7601 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for RG7601. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of RG7601 through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [6]
Thymoquinone [Phase 2/3]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for Thymoquinone. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Thymoquinone through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [7]
APG-1252 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for APG-1252. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of APG-1252 through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [8]
APG-2575 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for APG-2575. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of APG-2575 through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [9]
AZD0466 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for AZD0466. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AZD0466 through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [10]
Beclanorsen [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for Beclanorsen. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Beclanorsen through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [11]
Gossypol [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for Gossypol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Gossypol through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [12]
Obatoclax [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for Obatoclax. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Obatoclax through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [13]
PNT-2258 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for PNT-2258. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PNT-2258 through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [14]
AI-850 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for AI-850. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AI-850 through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [15]
BCL201 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for BCL201. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BCL201 through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [16]
BGB-11417 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for BGB-11417. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BGB-11417 through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [17]
BP1002 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for BP1002. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BP1002 through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [18]
LP-108 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for LP-108. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LP-108 through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [19]
Pc4 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for Pc4. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Pc4 through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [20]
VOB560 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for VOB560. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of VOB560 through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [21]
2,3,4-trihydroxy-5-isopropyl-N-phenyl-benzamide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for 2,3,4-trihydroxy-5-isopropyl-N-phenyl-benzamide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 2,3,4-trihydroxy-5-isopropyl-N-phenyl-benzamide through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [22]
4,5-dibenzylbenzene-1,2-diol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for 4,5-dibenzylbenzene-1,2-diol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 4,5-dibenzylbenzene-1,2-diol through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [23]
5,10-Dioxy-2-phenyl-benzo[g]pteridin-4-ylamine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for 5,10-Dioxy-2-phenyl-benzo[g]pteridin-4-ylamine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 5,10-Dioxy-2-phenyl-benzo[g]pteridin-4-ylamine through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [24]
Apogossypol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for Apogossypol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Apogossypol through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [25]
BP-100-1.02 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for BP-100-1.02. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BP-100-1.02 through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [26]
modified HA14-1 compounds (cancer) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for modified HA14-1 compounds (cancer). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of modified HA14-1 compounds (cancer) through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [24]
N-phenyl-2,3,4-trihydroxy-5-benzyl-benzamide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for N-phenyl-2,3,4-trihydroxy-5-benzyl-benzamide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-phenyl-2,3,4-trihydroxy-5-benzyl-benzamide through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [24]
QEDIIRNIARHLAQVGDSMDR [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for QEDIIRNIARHLAQVGDSMDR. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of QEDIIRNIARHLAQVGDSMDR through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [24]
TW-37 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for TW-37. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of TW-37 through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [27]
WL-276 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for WL-276. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of WL-276 through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [28]
ABT-737 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Apoptosis regulator Bcl-2 (BCL-2) is a therapeutic target for ABT-737. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ABT-737 through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [29]
ATP-citrate synthase (ACLY)
Bempedoic acid [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary ATP-citrate synthase (ACLY) is a therapeutic target for Bempedoic acid. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Bempedoic acid through regulating the expression of ATP-citrate synthase (ACLY). [30], [31]
(-)-hydroxycitrate [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary ATP-citrate synthase (ACLY) is a therapeutic target for (-)-hydroxycitrate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of (-)-hydroxycitrate through regulating the expression of ATP-citrate synthase (ACLY). [30], [32]
SB-201076 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary ATP-citrate synthase (ACLY) is a therapeutic target for SB-201076. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SB-201076 through regulating the expression of ATP-citrate synthase (ACLY). [30], [33]
Beta-catenin (CTNNB1)
Recombinant human endostatin [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Beta-catenin (CTNNB1) is a therapeutic target for Recombinant human endostatin. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Recombinant human endostatin through regulating the expression of Beta-catenin (CTNNB1). [34], [35]
C 82 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Beta-catenin (CTNNB1) is a therapeutic target for C 82. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of C 82 through regulating the expression of Beta-catenin (CTNNB1). [34], [36]
CEQ-508 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Beta-catenin (CTNNB1) is a therapeutic target for CEQ-508. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CEQ-508 through regulating the expression of Beta-catenin (CTNNB1). [34], [37]
C-X-C chemokine receptor type 4 (CXCR4)
Plerixafor [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Plerixafor. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Plerixafor through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [39]
AMD-070 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for AMD-070. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AMD-070 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [40]
Balixafortide [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Balixafortide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Balixafortide through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [4], [38]
BL-8040 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for BL-8040. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BL-8040 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [41]
Ulocuplumab [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Ulocuplumab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ulocuplumab through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [42]
CTCE-9908 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for CTCE-9908. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CTCE-9908 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [15], [38]
POL-6326 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for POL-6326. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of POL-6326 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [43]
TG-0054 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for TG-0054. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of TG-0054 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [44]
USL311 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for USL311. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of USL311 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [45]
ALX-0651 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for ALX-0651. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ALX-0651 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [46]
BMS-936564 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for BMS-936564. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BMS-936564 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [41]
CTCE-0214 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for CTCE-0214. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CTCE-0214 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [47]
GMI-1359 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for GMI-1359. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of GMI-1359 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [48]
LY2624587 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for LY2624587. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LY2624587 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [49]
MSX-122 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for MSX-122. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MSX-122 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [50]
PF-06747143 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for PF-06747143. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PF-06747143 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [51]
MAb173 [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for MAb173. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MAb173 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [52]
AT-009 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for AT-009. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AT-009 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [53]
ATI-2341 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for ATI-2341. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ATI-2341 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [53]
CTCE-0324 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for CTCE-0324. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CTCE-0324 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [54]
CX-02 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for CX-02. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CX-02 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [53]
CXCL8 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for CXCL8. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CXCL8 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [55]
CXCR4 gene disrupted T cells [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for CXCR4 gene disrupted T cells. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CXCR4 gene disrupted T cells through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [53]
Cyclo(-D-Ala-D-Arg-L-Arg-L-Nal-Gly-) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Cyclo(-D-Ala-D-Arg-L-Arg-L-Nal-Gly-). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclo(-D-Ala-D-Arg-L-Arg-L-Nal-Gly-) through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [56]
Cyclo(-D-MeTyr-D-Arg-L-Arg-L-Nal-Gly-) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Cyclo(-D-MeTyr-D-Arg-L-Arg-L-Nal-Gly-). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclo(-D-MeTyr-D-Arg-L-Arg-L-Nal-Gly-) through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [56]
Cyclo(-D-MeTyr-L-Arg-L-Arg-L-Nal-Gly-) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Cyclo(-D-MeTyr-L-Arg-L-Arg-L-Nal-Gly-). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclo(-D-MeTyr-L-Arg-L-Arg-L-Nal-Gly-) through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [56]
Cyclo(-D-Tyr-Arg-Arg-Nal-Gly-) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Cyclo(-D-Tyr-Arg-Arg-Nal-Gly-). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclo(-D-Tyr-Arg-Arg-Nal-Gly-) through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [57]
Cyclo(-D-Tyr-D-Ala-L-Arg-L-Nal-Gly-) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Cyclo(-D-Tyr-D-Ala-L-Arg-L-Nal-Gly-). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclo(-D-Tyr-D-Ala-L-Arg-L-Nal-Gly-) through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [56]
Cyclo(-D-Tyr-D-Arg-L-Arg-L-MeNal-Gly-) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Cyclo(-D-Tyr-D-Arg-L-Arg-L-MeNal-Gly-). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclo(-D-Tyr-D-Arg-L-Arg-L-MeNal-Gly-) through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [56]
Cyclo(-D-Tyr-D-Arg-L-Arg-L-Nal-beta-Ala-) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Cyclo(-D-Tyr-D-Arg-L-Arg-L-Nal-beta-Ala-). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclo(-D-Tyr-D-Arg-L-Arg-L-Nal-beta-Ala-) through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [56]
Cyclo(-D-Tyr-D-Arg-L-Arg-L-Nal-D-Ala-) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Cyclo(-D-Tyr-D-Arg-L-Arg-L-Nal-D-Ala-). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclo(-D-Tyr-D-Arg-L-Arg-L-Nal-D-Ala-) through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [56]
Cyclo(-D-Tyr-D-Arg-L-Arg-L-Nal-Gly-) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Cyclo(-D-Tyr-D-Arg-L-Arg-L-Nal-Gly-). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclo(-D-Tyr-D-Arg-L-Arg-L-Nal-Gly-) through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [58]
Cyclo(-D-Tyr-D-Arg-L-Arg-L-Nal-L-Ala-) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Cyclo(-D-Tyr-D-Arg-L-Arg-L-Nal-L-Ala-). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclo(-D-Tyr-D-Arg-L-Arg-L-Nal-L-Ala-) through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [56]
Cyclo(-D-Tyr-D-Arg-L-Arg-L-Nal-L-Pic-) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Cyclo(-D-Tyr-D-Arg-L-Arg-L-Nal-L-Pic-). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclo(-D-Tyr-D-Arg-L-Arg-L-Nal-L-Pic-) through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [56]
Cyclo(-D-Tyr-D-Arg-L-Arg-L-Nal-Sar-) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Cyclo(-D-Tyr-D-Arg-L-Arg-L-Nal-Sar-). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclo(-D-Tyr-D-Arg-L-Arg-L-Nal-Sar-) through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [56]
Cyclo(-D-Tyr-D-Arg-L-MeArg-L-Nal-Gly-) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Cyclo(-D-Tyr-D-Arg-L-MeArg-L-Nal-Gly-). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclo(-D-Tyr-D-Arg-L-MeArg-L-Nal-Gly-) through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [56]
Cyclo(-D-Tyr-D-MeArg-L-Arg-L-Nal-Gly-) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Cyclo(-D-Tyr-D-MeArg-L-Arg-L-Nal-Gly-). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclo(-D-Tyr-D-MeArg-L-Arg-L-Nal-Gly-) through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [56]
Cyclo(-D-Tyr-L-Ala-L-Arg-L-Nal-Gly-) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Cyclo(-D-Tyr-L-Ala-L-Arg-L-Nal-Gly-). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclo(-D-Tyr-L-Ala-L-Arg-L-Nal-Gly-) through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [56]
Cyclo(-D-Tyr-L-Arg-L-Arg-L-Ala-Sar-) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Cyclo(-D-Tyr-L-Arg-L-Arg-L-Ala-Sar-). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclo(-D-Tyr-L-Arg-L-Arg-L-Ala-Sar-) through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [56]
Cyclo(-D-Tyr-L-Arg-L-Arg-L-MeNal-Gly-) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Cyclo(-D-Tyr-L-Arg-L-Arg-L-MeNal-Gly-). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclo(-D-Tyr-L-Arg-L-Arg-L-MeNal-Gly-) through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [56]
Cyclo(-D-Tyr-L-Arg-L-Arg-L-Nal-beta-Ala-) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Cyclo(-D-Tyr-L-Arg-L-Arg-L-Nal-beta-Ala-). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclo(-D-Tyr-L-Arg-L-Arg-L-Nal-beta-Ala-) through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [56]
Cyclo(-D-Tyr-L-Arg-L-Arg-L-Nal-D-Ala-) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Cyclo(-D-Tyr-L-Arg-L-Arg-L-Nal-D-Ala-). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclo(-D-Tyr-L-Arg-L-Arg-L-Nal-D-Ala-) through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [56]
Cyclo(-D-Tyr-L-Arg-L-Arg-L-Nal-Gly-) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Cyclo(-D-Tyr-L-Arg-L-Arg-L-Nal-Gly-). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclo(-D-Tyr-L-Arg-L-Arg-L-Nal-Gly-) through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [56]
Cyclo(-D-Tyr-L-Arg-L-Arg-L-Nal-L-Ala-) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Cyclo(-D-Tyr-L-Arg-L-Arg-L-Nal-L-Ala-). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclo(-D-Tyr-L-Arg-L-Arg-L-Nal-L-Ala-) through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [56]
Cyclo(-D-Tyr-L-Arg-L-MeArg-L-Nal-Gly-) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Cyclo(-D-Tyr-L-Arg-L-MeArg-L-Nal-Gly-). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclo(-D-Tyr-L-Arg-L-MeArg-L-Nal-Gly-) through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [56]
Cyclo(-D-Tyr-L-MeArg-L-Arg-L-Nal-Gly-) [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Cyclo(-D-Tyr-L-MeArg-L-Arg-L-Nal-Gly-). The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclo(-D-Tyr-L-MeArg-L-Arg-L-Nal-Gly-) through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [56]
GSK-812397 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for GSK-812397. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of GSK-812397 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [53]
isothiourea-1a [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for isothiourea-1a. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of isothiourea-1a through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [54]
isothiourea-1t [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for isothiourea-1t. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of isothiourea-1t through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [59]
KUR-CXCR4 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for KUR-CXCR4. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of KUR-CXCR4 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [53]
LP-0067 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for LP-0067. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LP-0067 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [53]
NB-325 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for NB-325. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of NB-325 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [53]
ND-401 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for ND-401. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ND-401 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [53]
T134 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for T134. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of T134 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [59]
T140 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for T140. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of T140 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [59]
T22 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for T22. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of T22 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [60]
TN-14003 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for TN-14003. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of TN-14003 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [56]
viral macrophage inflammatory protein-II [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for viral macrophage inflammatory protein-II. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of viral macrophage inflammatory protein-II through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [61]
Garnocestim [Discontinued in Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for Garnocestim. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Garnocestim through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [62]
KRH-2731 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for KRH-2731. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of KRH-2731 through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [63]
SURADISTA [Discontinued in Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C chemokine receptor type 4 (CXCR4) is a therapeutic target for SURADISTA. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SURADISTA through regulating the expression of C-X-C chemokine receptor type 4 (CXCR4). [38], [64]
C-X-C motif chemokine 10 (CXCL10)
Anti-IP10 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C motif chemokine 10 (CXCL10) is a therapeutic target for Anti-IP10. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Anti-IP10 through regulating the expression of C-X-C motif chemokine 10 (CXCL10). [37], [65]
BMS-936557 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C motif chemokine 10 (CXCL10) is a therapeutic target for BMS-936557. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BMS-936557 through regulating the expression of C-X-C motif chemokine 10 (CXCL10). [65], [66]
JT02 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C motif chemokine 10 (CXCL10) is a therapeutic target for JT02. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of JT02 through regulating the expression of C-X-C motif chemokine 10 (CXCL10). [65], [67]
MDX-1100 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C motif chemokine 10 (CXCL10) is a therapeutic target for MDX-1100. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MDX-1100 through regulating the expression of C-X-C motif chemokine 10 (CXCL10). [65], [68]
NI-0801 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C motif chemokine 10 (CXCL10) is a therapeutic target for NI-0801. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of NI-0801 through regulating the expression of C-X-C motif chemokine 10 (CXCL10). [65], [69]
NG-641 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C motif chemokine 10 (CXCL10) is a therapeutic target for NG-641. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of NG-641 through regulating the expression of C-X-C motif chemokine 10 (CXCL10). [65], [68]
N-Methylleucine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C motif chemokine 10 (CXCL10) is a therapeutic target for N-Methylleucine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-Methylleucine through regulating the expression of C-X-C motif chemokine 10 (CXCL10). [65], [70]
C-X-C motif chemokine 9 (CXCL9)
NG-641 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary C-X-C motif chemokine 9 (CXCL9) is a therapeutic target for NG-641. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of NG-641 through regulating the expression of C-X-C motif chemokine 9 (CXCL9). [65], [71]
C/EBP beta messenger RNA (CEBPB mRNA)
ISIS 116505 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C/EBP beta messenger RNA (CEBPB mRNA) is a therapeutic target for ISIS 116505. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 116505 through regulating the expression of C/EBP beta messenger RNA (CEBPB mRNA). [72], [73]
ISIS 116507 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C/EBP beta messenger RNA (CEBPB mRNA) is a therapeutic target for ISIS 116507. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 116507 through regulating the expression of C/EBP beta messenger RNA (CEBPB mRNA). [72], [73]
ISIS 116508 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary C/EBP beta messenger RNA (CEBPB mRNA) is a therapeutic target for ISIS 116508. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 116508 through regulating the expression of C/EBP beta messenger RNA (CEBPB mRNA). [72], [74]
Calmodulin-dependent kinase II (CAMKK2)
STO609 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Calmodulin-dependent kinase II (CAMKK2) is a therapeutic target for STO609. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of STO609 through regulating the expression of Calmodulin-dependent kinase II (CAMKK2). [75], [76]
Caspase-3 (CASP3)
PAC1 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Caspase-3 (CASP3) is a therapeutic target for PAC1. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PAC1 through regulating the expression of Caspase-3 (CASP3). [77], [78]
2-(4-fluoro-benzyl)isoquinoline-1,3,4-trione [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Caspase-3 (CASP3) is a therapeutic target for 2-(4-fluoro-benzyl)isoquinoline-1,3,4-trione. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 2-(4-fluoro-benzyl)isoquinoline-1,3,4-trione through regulating the expression of Caspase-3 (CASP3). [77], [79]
2-(4-methoxy-benzyl)isoquinoline-1,3,4-trione [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Caspase-3 (CASP3) is a therapeutic target for 2-(4-methoxy-benzyl)isoquinoline-1,3,4-trione. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 2-(4-methoxy-benzyl)isoquinoline-1,3,4-trione through regulating the expression of Caspase-3 (CASP3). [77], [79]
2-allylisoquinoline-1,3,4-trione [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Caspase-3 (CASP3) is a therapeutic target for 2-allylisoquinoline-1,3,4-trione. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 2-allylisoquinoline-1,3,4-trione through regulating the expression of Caspase-3 (CASP3). [77], [79]
2-benzylisoquinoline-1,3,4-trione [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Caspase-3 (CASP3) is a therapeutic target for 2-benzylisoquinoline-1,3,4-trione. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 2-benzylisoquinoline-1,3,4-trione through regulating the expression of Caspase-3 (CASP3). [77], [79]
2-methylisoquinoline-1,3,4-trione [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Caspase-3 (CASP3) is a therapeutic target for 2-methylisoquinoline-1,3,4-trione. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 2-methylisoquinoline-1,3,4-trione through regulating the expression of Caspase-3 (CASP3). [77], [80]
2-phenethylisoquinoline-1,3,4-trione [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Caspase-3 (CASP3) is a therapeutic target for 2-phenethylisoquinoline-1,3,4-trione. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 2-phenethylisoquinoline-1,3,4-trione through regulating the expression of Caspase-3 (CASP3). [77], [79]
5-(azepan-1-ylsulfonyl)indoline-2,3-dione [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Caspase-3 (CASP3) is a therapeutic target for 5-(azepan-1-ylsulfonyl)indoline-2,3-dione. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 5-(azepan-1-ylsulfonyl)indoline-2,3-dione through regulating the expression of Caspase-3 (CASP3). [77], [80]
5-(azetidin-1-ylsulfonyl)indoline-2,3-dione [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Caspase-3 (CASP3) is a therapeutic target for 5-(azetidin-1-ylsulfonyl)indoline-2,3-dione. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 5-(azetidin-1-ylsulfonyl)indoline-2,3-dione through regulating the expression of Caspase-3 (CASP3). [77], [80]
5-(piperidin-1-ylsulfonyl)indoline-2,3-dione [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Caspase-3 (CASP3) is a therapeutic target for 5-(piperidin-1-ylsulfonyl)indoline-2,3-dione. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 5-(piperidin-1-ylsulfonyl)indoline-2,3-dione through regulating the expression of Caspase-3 (CASP3). [77], [80]
5-(pyrrolidin-1-ylsulfonyl)indoline-2,3-dione [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Caspase-3 (CASP3) is a therapeutic target for 5-(pyrrolidin-1-ylsulfonyl)indoline-2,3-dione. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 5-(pyrrolidin-1-ylsulfonyl)indoline-2,3-dione through regulating the expression of Caspase-3 (CASP3). [77], [81]
Ac-Asp-Glu-Val-Asp-CHO [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Caspase-3 (CASP3) is a therapeutic target for Ac-Asp-Glu-Val-Asp-CHO. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ac-Asp-Glu-Val-Asp-CHO through regulating the expression of Caspase-3 (CASP3). [77], [79]
Ac-DEVD-CHO [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Caspase-3 (CASP3) is a therapeutic target for Ac-DEVD-CHO. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ac-DEVD-CHO through regulating the expression of Caspase-3 (CASP3). [77], [82]
AZ10417808 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Caspase-3 (CASP3) is a therapeutic target for AZ10417808. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AZ10417808 through regulating the expression of Caspase-3 (CASP3). [77], [83]
Glionitrin A [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Caspase-3 (CASP3) is a therapeutic target for Glionitrin A. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Glionitrin A through regulating the expression of Caspase-3 (CASP3). [77], [84]
Isoquinoline-1,3,4(2H)-trione [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Caspase-3 (CASP3) is a therapeutic target for Isoquinoline-1,3,4(2H)-trione. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Isoquinoline-1,3,4(2H)-trione through regulating the expression of Caspase-3 (CASP3). [77], [79]
M826 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Caspase-3 (CASP3) is a therapeutic target for M826. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of M826 through regulating the expression of Caspase-3 (CASP3). [77], [85]
PETCM [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Caspase-3 (CASP3) is a therapeutic target for PETCM. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PETCM through regulating the expression of Caspase-3 (CASP3). [77], [86]
SJ-8002 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Caspase-3 (CASP3) is a therapeutic target for SJ-8002. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SJ-8002 through regulating the expression of Caspase-3 (CASP3). [77], [87]
CEBPA messenger RNA (CEBPA mRNA)
MTL-CEPBA [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary CEBPA messenger RNA (CEBPA mRNA) is a therapeutic target for MTL-CEPBA. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MTL-CEPBA through regulating the expression of CEBPA messenger RNA (CEBPA mRNA). [72], [88]
Cellular tumor antigen p53 (TP53)
Contusugene ladenovec [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for Contusugene ladenovec. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Contusugene ladenovec through regulating the expression of Cellular tumor antigen p53 (TP53). [89], [90]
QPI-1002 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for QPI-1002. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of QPI-1002 through regulating the expression of Cellular tumor antigen p53 (TP53). [89], [91]
Thymoquinone [Phase 2/3]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for Thymoquinone. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Thymoquinone through regulating the expression of Cellular tumor antigen p53 (TP53). [89], [92]
Ad-p53 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for Ad-p53. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ad-p53 through regulating the expression of Cellular tumor antigen p53 (TP53). [89], [93]
ALT-801 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for ALT-801. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ALT-801 through regulating the expression of Cellular tumor antigen p53 (TP53). [89], [94]
APG-115 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for APG-115. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of APG-115 through regulating the expression of Cellular tumor antigen p53 (TP53). [89], [95]
APR-246 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for APR-246. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of APR-246 through regulating the expression of Cellular tumor antigen p53 (TP53). [89], [96]
Cenersen [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for Cenersen. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cenersen through regulating the expression of Cellular tumor antigen p53 (TP53). [89], [97]
INGN-225 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for INGN-225. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of INGN-225 through regulating the expression of Cellular tumor antigen p53 (TP53). [15], [89]
ISA-P53-01 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for ISA-P53-01. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISA-P53-01 through regulating the expression of Cellular tumor antigen p53 (TP53). [89], [98]
Kevetrin [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for Kevetrin. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Kevetrin through regulating the expression of Cellular tumor antigen p53 (TP53). [13], [89]
OPI-1002 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for OPI-1002. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of OPI-1002 through regulating the expression of Cellular tumor antigen p53 (TP53). [89], [99]
SGT-53 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for SGT-53. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SGT-53 through regulating the expression of Cellular tumor antigen p53 (TP53). [15], [89]
CGM097 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for CGM097. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CGM097 through regulating the expression of Cellular tumor antigen p53 (TP53). [15], [89]
COTI-2 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for COTI-2. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of COTI-2 through regulating the expression of Cellular tumor antigen p53 (TP53). [89], [100]
Dendritic cell vaccine [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for Dendritic cell vaccine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Dendritic cell vaccine through regulating the expression of Cellular tumor antigen p53 (TP53). [89], [101]
HDM201 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for HDM201. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of HDM201 through regulating the expression of Cellular tumor antigen p53 (TP53). [89], [102]
ONYX-015 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for ONYX-015. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ONYX-015 through regulating the expression of Cellular tumor antigen p53 (TP53). [89], [103]
SAR-405838 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for SAR-405838. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SAR-405838 through regulating the expression of Cellular tumor antigen p53 (TP53). [89], [90]
1-(9-ethyl-9H-carbazol-3-yl)-N-methylmethanamine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for 1-(9-ethyl-9H-carbazol-3-yl)-N-methylmethanamine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 1-(9-ethyl-9H-carbazol-3-yl)-N-methylmethanamine through regulating the expression of Cellular tumor antigen p53 (TP53). [89], [104]
AHL [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for AHL. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AHL through regulating the expression of Cellular tumor antigen p53 (TP53). [89], [105]
NU-8231 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for NU-8231. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of NU-8231 through regulating the expression of Cellular tumor antigen p53 (TP53). [89], [106]
NUTLIN-3 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for NUTLIN-3. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of NUTLIN-3 through regulating the expression of Cellular tumor antigen p53 (TP53). [89], [107]
INGN-234 [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for INGN-234. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of INGN-234 through regulating the expression of Cellular tumor antigen p53 (TP53). [89], [108]
Pifithrin-alpha [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for Pifithrin-alpha. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Pifithrin-alpha through regulating the expression of Cellular tumor antigen p53 (TP53). [89], [109]
TAR-1 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Cellular tumor antigen p53 (TP53) is a therapeutic target for TAR-1. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of TAR-1 through regulating the expression of Cellular tumor antigen p53 (TP53). [89], [110]
Cystine/glutamate transporter (SLC7A11)
L-glutamic acid [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cystine/glutamate transporter (SLC7A11) is a therapeutic target for L-glutamic acid. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of L-glutamic acid through regulating the expression of Cystine/glutamate transporter (SLC7A11). [34], [111]
SXC-2023 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Cystine/glutamate transporter (SLC7A11) is a therapeutic target for SXC-2023. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SXC-2023 through regulating the expression of Cystine/glutamate transporter (SLC7A11). [34], [112]
Cytochrome P450 1B1 (CYP1B1)
Amodiaquine [Phase 4]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for Amodiaquine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Amodiaquine through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [113]
Caffeine [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for Caffeine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Caffeine through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [114]
Erythromycin stearate [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for Erythromycin stearate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Erythromycin stearate through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [115]
Estrone [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for Estrone. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Estrone through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [116]
Flutamide [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for Flutamide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Flutamide through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [117]
Hydrogen peroxide [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for Hydrogen peroxide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Hydrogen peroxide through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [118]
Melatonin [Phase 4]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for Melatonin. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Melatonin through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [119]
Oxaliplatin [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for Oxaliplatin. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Oxaliplatin through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [120]
Procarbazine [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for Procarbazine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Procarbazine through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [121]
Progesterone [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for Progesterone. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Progesterone through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [122]
Rosuvastatin [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for Rosuvastatin. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Rosuvastatin through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [123]
Testosterone cypionate [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for Testosterone cypionate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Testosterone cypionate through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [122]
Theophylline [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for Theophylline. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Theophylline through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [114]
Estradiol [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for Estradiol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Estradiol through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [124]
HSDB-3466 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for HSDB-3466. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of HSDB-3466 through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [125]
NSC-122758 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for NSC-122758. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of NSC-122758 through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [126]
PINOCEMBRIN [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for PINOCEMBRIN. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PINOCEMBRIN through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [127]
Naringenin [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for Naringenin. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Naringenin through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [128]
2-[2-(3,5-Dimethoxy-phenyl)-vinyl]-thiophene [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for 2-[2-(3,5-Dimethoxy-phenyl)-vinyl]-thiophene. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 2-[2-(3,5-Dimethoxy-phenyl)-vinyl]-thiophene through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [129]
3-[2-(3,5-Dimethoxy-phenyl)-vinyl]-furan [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for 3-[2-(3,5-Dimethoxy-phenyl)-vinyl]-furan. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 3-[2-(3,5-Dimethoxy-phenyl)-vinyl]-furan through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [129]
4-[2-(3,5-Dimethoxy-phenyl)-vinyl]-pyridine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for 4-[2-(3,5-Dimethoxy-phenyl)-vinyl]-pyridine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 4-[2-(3,5-Dimethoxy-phenyl)-vinyl]-pyridine through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [129]
ACACETIN [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for ACACETIN. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ACACETIN through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [128]
APIGENIN [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for APIGENIN. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of APIGENIN through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [128]
Chrysin [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for Chrysin. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Chrysin through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [128]
CHRYSOERIOL [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for CHRYSOERIOL. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CHRYSOERIOL through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [128]
Dibutylphthalate [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for Dibutylphthalate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Dibutylphthalate through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [130]
DIOSMETIN [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for DIOSMETIN. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of DIOSMETIN through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [128]
ERIODICTYOL [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for ERIODICTYOL. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ERIODICTYOL through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [128]
Galangin [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for Galangin. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Galangin through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [129]
HOMOERIODICTYOL [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for HOMOERIODICTYOL. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of HOMOERIODICTYOL through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [128]
ISORHAMNETIN [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for ISORHAMNETIN. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISORHAMNETIN through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [128]
ISOSAKUTANETIN [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for ISOSAKUTANETIN. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISOSAKUTANETIN through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [128]
KAEMPFERIDE [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for KAEMPFERIDE. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of KAEMPFERIDE through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [128]
KAEMPFEROL [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for KAEMPFEROL. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of KAEMPFEROL through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [128]
N-(2,4-Dimethoxy-phenyl)-3,5-dimethoxy-benzamide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for N-(2,4-Dimethoxy-phenyl)-3,5-dimethoxy-benzamide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-(2,4-Dimethoxy-phenyl)-3,5-dimethoxy-benzamide through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [128]
TAMARIXETIN [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for TAMARIXETIN. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of TAMARIXETIN through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [128]
TRISMETHOXYRESVERATROL [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 1B1 (CYP1B1) is a therapeutic target for TRISMETHOXYRESVERATROL. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of TRISMETHOXYRESVERATROL through regulating the expression of Cytochrome P450 1B1 (CYP1B1). [38], [129]
Cytochrome P450 2C8 (CYP2C8)
Almotriptan malate [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Almotriptan malate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Almotriptan malate through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [132]
Aminophenazone [Phase 4]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Aminophenazone. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Aminophenazone through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [133]
Amiodarone hydrochloride [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Amiodarone hydrochloride. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Amiodarone hydrochloride through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [134]
Amitriptyline hydrochloride [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Amitriptyline hydrochloride. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Amitriptyline hydrochloride through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [135]
Amodiaquine [Phase 4]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Amodiaquine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Amodiaquine through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [136]
Anastrozole [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Anastrozole. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Anastrozole through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [137]
Apalutamide [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Apalutamide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Apalutamide through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [138]
Apixaban [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Apixaban. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Apixaban through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [139]
Atorvastatin calcium [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Atorvastatin calcium. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Atorvastatin calcium through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [140]
Azelastine [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Azelastine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Azelastine through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [141]
Benzyl alcohol [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Benzyl alcohol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Benzyl alcohol through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [142]
Beraprost [Phase 4]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Beraprost. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Beraprost through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [143]
Brigatinib [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Brigatinib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Brigatinib through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [144]
Bromfenac [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Bromfenac. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Bromfenac through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [145]
Buprenorphine hydrochloride [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Buprenorphine hydrochloride. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Buprenorphine hydrochloride through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [146]
Cabazitaxel [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Cabazitaxel. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cabazitaxel through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [147]
Caffeine [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Caffeine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Caffeine through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [148]
Capsaicin [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Capsaicin. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Capsaicin through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [149]
Carbamazepine [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Carbamazepine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Carbamazepine through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [150]
Cefaloridine [Phase 4]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Cefaloridine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cefaloridine through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [151]
Celecoxib [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Celecoxib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Celecoxib through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [152]
Cerivastatin sodium [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Cerivastatin sodium. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cerivastatin sodium through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [140]
Cisapride [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Cisapride. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cisapride through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [153]
Clozapine [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Clozapine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Clozapine through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [154]
Cyclophosphamide [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Cyclophosphamide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyclophosphamide through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [155]
Dabrafenib mesylate [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Dabrafenib mesylate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Dabrafenib mesylate through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [140]
Dapsone [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Dapsone. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Dapsone through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [156]
Desloratadine [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Desloratadine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Desloratadine through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [157]
Dexibuprofen [Phase 4]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Dexibuprofen. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Dexibuprofen through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [158]
Diazepam [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Diazepam. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Diazepam through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [159]
Diclofenac sodium [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Diclofenac sodium. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Diclofenac sodium through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [160]
Diethylstilbestrol [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Diethylstilbestrol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Diethylstilbestrol through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [161]
Diltiazem hydrochloride [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Diltiazem hydrochloride. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Diltiazem hydrochloride through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [162]
Eltrombopag olamine [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Eltrombopag olamine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Eltrombopag olamine through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [163]
Enasidenib [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Enasidenib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Enasidenib through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [164]
Enzalutamide [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Enzalutamide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Enzalutamide through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [140]
Estradiol acetate [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Estradiol acetate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Estradiol acetate through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [140]
Estradiol cypionate [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Estradiol cypionate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Estradiol cypionate through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [165]
Estradiol valerate [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Estradiol valerate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Estradiol valerate through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [165]
Eszopiclone [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Eszopiclone. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Eszopiclone through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [166]
Ethinyl estradiol [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Ethinyl estradiol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ethinyl estradiol through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [167]
Fluvastatin sodium [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Fluvastatin sodium. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Fluvastatin sodium through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [168]
Glasdegib [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Glasdegib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Glasdegib through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [169]
Halofantrine [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Halofantrine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Halofantrine through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [170]
Ibuprofen [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Ibuprofen. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ibuprofen through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [158]
Ifosfamide [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Ifosfamide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ifosfamide through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [155]
Imatinib mesylate [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Imatinib mesylate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Imatinib mesylate through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [140]
Irbesartan [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Irbesartan. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Irbesartan through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [167]
Istradefylline [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Istradefylline. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Istradefylline through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [171]
Ixazomib [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Ixazomib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ixazomib through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [172]
Ketobemidone [Phase 4]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Ketobemidone. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ketobemidone through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [173]
Ketorolac [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Ketorolac. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ketorolac through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [174]
Lansoprazole [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Lansoprazole. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Lansoprazole through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [175]
Lapatinib ditosylate [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Lapatinib ditosylate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Lapatinib ditosylate through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [176]
Levomilnacipran [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Levomilnacipran. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Levomilnacipran through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [177]
Lidocaine [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Lidocaine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Lidocaine through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [178]
Loperamide hydrochloride [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Loperamide hydrochloride. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Loperamide hydrochloride through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [179]
Loratadine [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Loratadine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Loratadine through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [140]
Lorlatinib [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Lorlatinib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Lorlatinib through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [180]
Losartan potassium [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Losartan potassium. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Losartan potassium through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [181]
Lovastatin [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Lovastatin. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Lovastatin through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [182]
Mefenamic acid [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Mefenamic acid. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Mefenamic acid through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [140]
Meloxicam [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Meloxicam. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Meloxicam through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [183]
Mephenytoin [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Mephenytoin. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Mephenytoin through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [184]
Mestranol [Phase 4]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Mestranol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Mestranol through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [185]
Methadone [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Methadone. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Methadone through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [186]
Mirtazapine [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Mirtazapine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Mirtazapine through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [178]
Montelukast sodium [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Montelukast sodium. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Montelukast sodium through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [187]
Morphine [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Morphine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Morphine through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [188]
Mycophenolate mofetil [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Mycophenolate mofetil. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Mycophenolate mofetil through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [189]
Naloxone [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Naloxone. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Naloxone through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [146]
Naproxen [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Naproxen. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Naproxen through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [190]
Nicardipine hydrochloride [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Nicardipine hydrochloride. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Nicardipine hydrochloride through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [178]
Nicotine [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Nicotine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Nicotine through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [191]
Nilotinib [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Nilotinib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Nilotinib through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [140]
Ombitasvir [Phase 4]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Ombitasvir. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ombitasvir through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [192]
Omeprazole [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Omeprazole. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Omeprazole through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [193]
Pazopanib [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Pazopanib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Pazopanib through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [194]
Pentamidine isethionate [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Pentamidine isethionate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Pentamidine isethionate through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [195]
Perphenazine [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Perphenazine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Perphenazine through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [196]
Phenobarbital [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Phenobarbital. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Phenobarbital through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [197]
Phenprocoumon [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Phenprocoumon. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Phenprocoumon through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [198]
Phenytoin [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Phenytoin. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Phenytoin through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [178]
Pioglitazone hydrochloride [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Pioglitazone hydrochloride. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Pioglitazone hydrochloride through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [199]
Piroxicam [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Piroxicam. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Piroxicam through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [200]
Pitavastatin calcium [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Pitavastatin calcium. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Pitavastatin calcium through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [201]
Propofol [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Propofol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Propofol through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [202]
Quinidine [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Quinidine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Quinidine through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [140]
Quinine sulfate [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Quinine sulfate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Quinine sulfate through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [140]
Repaglinide [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Repaglinide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Repaglinide through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [203]
Riociguat [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Riociguat. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Riociguat through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [204]
Rofecoxib [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Rofecoxib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Rofecoxib through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [140]
Rosiglitazone [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Rosiglitazone. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Rosiglitazone through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [205]
Selegiline hydrochloride [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Selegiline hydrochloride. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Selegiline hydrochloride through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [206]
Selexipag [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Selexipag. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Selexipag through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [207]
Simvastatin [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Simvastatin. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Simvastatin through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [208]
Sitagliptin [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Sitagliptin. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Sitagliptin through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [209]
Sulfadiazine [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Sulfadiazine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Sulfadiazine through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [210]
Sulfamethoxazole [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Sulfamethoxazole. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Sulfamethoxazole through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [211]
Sulfinpyrazone [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Sulfinpyrazone. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Sulfinpyrazone through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [178]
Tazarotene [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Tazarotene. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Tazarotene through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [212]
Tegafur [Phase 4]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Tegafur. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Tegafur through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [213]
Temazepam [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Temazepam. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Temazepam through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [214]
Terbinafine hydrochloride [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Terbinafine hydrochloride. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Terbinafine hydrochloride through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [166]
Testosterone cypionate [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Testosterone cypionate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Testosterone cypionate through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [140]
Testosterone enanthate [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Testosterone enanthate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Testosterone enanthate through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [140]
Testosterone undecanoate [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Testosterone undecanoate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Testosterone undecanoate through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [140]
Thalidomide [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Thalidomide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Thalidomide through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [215]
Tolbutamide [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Tolbutamide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Tolbutamide through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [216]
Torasemide [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Torasemide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Torasemide through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [217]
Treprostinil [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Treprostinil. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Treprostinil through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [218]
Trifarotene [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Trifarotene. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Trifarotene through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [219]
Trimethadione [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Trimethadione. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Trimethadione through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [220]
Trimethoprim [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Trimethoprim. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Trimethoprim through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [221]
Troglitazone [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Troglitazone. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Troglitazone through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [222]
Velpatasvir [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Velpatasvir. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Velpatasvir through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [223]
Verapamil hydrochloride [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Verapamil hydrochloride. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Verapamil hydrochloride through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [224]
Vortioxetine hydrobromide [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Vortioxetine hydrobromide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Vortioxetine hydrobromide through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [225]
Voxilaprevir [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Voxilaprevir. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Voxilaprevir through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [223]
Warfarin sodium [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Warfarin sodium. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Warfarin sodium through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [190]
Zafirlukast [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Zafirlukast. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Zafirlukast through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [221]
Zidovudine [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Zidovudine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Zidovudine through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [178]
Zopiclone [Phase 4]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Zopiclone. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Zopiclone through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [226]
BMS-298585 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for BMS-298585. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BMS-298585 through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [227]
BNP-1350 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for BNP-1350. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BNP-1350 through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [228]
CKD-501 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for CKD-501. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CKD-501 through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [229]
CYT-387 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for CYT-387. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CYT-387 through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [230]
Dasabuvir [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Dasabuvir. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Dasabuvir through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [231]
Domperidone [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Domperidone. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Domperidone through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [232]
DRF-2593 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for DRF-2593. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of DRF-2593 through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [229]
EMD-128130 [Phase 2/3]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for EMD-128130. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of EMD-128130 through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [233]
Estradiol [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Estradiol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Estradiol through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [140]
LAS-17177 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for LAS-17177. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LAS-17177 through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [234]
LAU-7b [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for LAU-7b. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LAU-7b through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [235]
LY-2484595 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for LY-2484595. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LY-2484595 through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [236]
NSC-122758 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for NSC-122758. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of NSC-122758 through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [237]
QLT-091001 [Phase 2/3]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for QLT-091001. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of QLT-091001 through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [237]
Rivoglitazone [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Rivoglitazone. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Rivoglitazone through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [238]
AZD-2014 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for AZD-2014. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AZD-2014 through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [239]
GSK-1278863 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for GSK-1278863. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of GSK-1278863 through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [240]
TAK-652 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for TAK-652. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of TAK-652 through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [241]
AG-1549 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for AG-1549. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AG-1549 through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [242]
AZD-9496 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for AZD-9496. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AZD-9496 through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [243]
H3B-6545 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for H3B-6545. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of H3B-6545 through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [244]
M-813 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for M-813. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of M-813 through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [245]
MK-0822 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for MK-0822. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MK-0822 through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [246]
Antipyrine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Antipyrine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Antipyrine through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [166]
Cyamemazine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Cyamemazine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cyamemazine through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [247]
Paraoxon [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Paraoxon. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Paraoxon through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [248]
ABT-001 [Discontinued]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for ABT-001. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ABT-001 through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [249]
ADD-3878 [Discontinued]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for ADD-3878. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ADD-3878 through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [229]
Aleglitazar [Discontinued in Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for Aleglitazar. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Aleglitazar through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [250]
ML-3000 [Discontinued]
In total 1 mechanisms lead to this potential drug response
Response Summary Cytochrome P450 2C8 (CYP2C8) is a therapeutic target for ML-3000. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ML-3000 through regulating the expression of Cytochrome P450 2C8 (CYP2C8). [131], [166]
DNA-binding factor KBF1 (p105)
CAT 1004 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary DNA-binding factor KBF1 (p105) is a therapeutic target for CAT 1004. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CAT 1004 through regulating the expression of DNA-binding factor KBF1 (p105). [251], [252]
P54 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary DNA-binding factor KBF1 (p105) is a therapeutic target for P54. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of P54 through regulating the expression of DNA-binding factor KBF1 (p105). [251], [253]
Dual-specificity tyrosine-phosphorylation regulated kinase 1A (DYRK1A)
KH-CB19 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Dual-specificity tyrosine-phosphorylation regulated kinase 1A (DYRK1A) is a therapeutic target for KH-CB19. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of KH-CB19 through regulating the expression of Dual-specificity tyrosine-phosphorylation regulated kinase 1A (DYRK1A). [254], [255]
leucettine L41 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Dual-specificity tyrosine-phosphorylation regulated kinase 1A (DYRK1A) is a therapeutic target for leucettine L41. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of leucettine L41 through regulating the expression of Dual-specificity tyrosine-phosphorylation regulated kinase 1A (DYRK1A). [254], [256]
ML315 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Dual-specificity tyrosine-phosphorylation regulated kinase 1A (DYRK1A) is a therapeutic target for ML315. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ML315 through regulating the expression of Dual-specificity tyrosine-phosphorylation regulated kinase 1A (DYRK1A). [254], [257]
WO2013026806C72 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Dual-specificity tyrosine-phosphorylation regulated kinase 1A (DYRK1A) is a therapeutic target for WO2013026806C72 . The Methyltransferase-like 14 (METTL14) has potential in affecting the response of WO2013026806C72 through regulating the expression of Dual-specificity tyrosine-phosphorylation regulated kinase 1A (DYRK1A). [254], [256]
Ephrin type-A receptor 3 (EPHA3)
Ifabotuzumab [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Ephrin type-A receptor 3 (EPHA3) is a therapeutic target for Ifabotuzumab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ifabotuzumab through regulating the expression of Ephrin type-A receptor 3 (EPHA3). [258], [259]
KB-004 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Ephrin type-A receptor 3 (EPHA3) is a therapeutic target for KB-004. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of KB-004 through regulating the expression of Ephrin type-A receptor 3 (EPHA3). [258], [260]
Ephrin type-B receptor 2 (EPHB2)
BVD-523 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Ephrin type-B receptor 2 (EPHB2) is a therapeutic target for BVD-523. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BVD-523 through regulating the expression of Ephrin type-B receptor 2 (EPHB2). [261], [262]
SEphB4-HSA [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Ephrin type-B receptor 2 (EPHB2) is a therapeutic target for SEphB4-HSA. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SEphB4-HSA through regulating the expression of Ephrin type-B receptor 2 (EPHB2). [261], [263]
KO-947 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Ephrin type-B receptor 2 (EPHB2) is a therapeutic target for KO-947. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of KO-947 through regulating the expression of Ephrin type-B receptor 2 (EPHB2). [15], [261]
MK-8353 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Ephrin type-B receptor 2 (EPHB2) is a therapeutic target for MK-8353. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MK-8353 through regulating the expression of Ephrin type-B receptor 2 (EPHB2). [15], [261]
AMP-PNP [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Ephrin type-B receptor 2 (EPHB2) is a therapeutic target for AMP-PNP. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AMP-PNP through regulating the expression of Ephrin type-B receptor 2 (EPHB2). [261], [264]
SNEWIQPRLPQH [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Ephrin type-B receptor 2 (EPHB2) is a therapeutic target for SNEWIQPRLPQH. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SNEWIQPRLPQH through regulating the expression of Ephrin type-B receptor 2 (EPHB2). [15], [261]
Epidermal growth factor receptor (EGFR)
Afatinib [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Afatinib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Afatinib through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [266]
Cetuximab [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Cetuximab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cetuximab through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [267]
Dacomitinib [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Dacomitinib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Dacomitinib through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [268]
Epidermal growth factor [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Epidermal growth factor. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Epidermal growth factor through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [269]
HEGF [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for HEGF. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of HEGF through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [270]
Icotinib hydrochloride [Registered]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Icotinib hydrochloride. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Icotinib hydrochloride through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [271]
Lapatinib [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Lapatinib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Lapatinib through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [272]
Merimepodib [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Merimepodib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Merimepodib through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [273]
Necitumumab [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Necitumumab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Necitumumab through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [274]
NERATINIB MALEATE [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for NERATINIB MALEATE. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of NERATINIB MALEATE through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [275]
Nitroglycerin [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Nitroglycerin. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Nitroglycerin through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [273]
Panitumumab [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Panitumumab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Panitumumab through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [276]
SKI-758 [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for SKI-758. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SKI-758 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
Vandetanib [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Vandetanib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Vandetanib through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [278]
AC0010 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for AC0010. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AC0010 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [279]
Almonertinib [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Almonertinib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Almonertinib through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [280]
Amivantamab [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Amivantamab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Amivantamab through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [281]
ASP1929 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for ASP1929. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ASP1929 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [282]
CO-1686 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for CO-1686. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CO-1686 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
DE-766 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for DE-766. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of DE-766 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [283]
EGF816 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for EGF816. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of EGF816 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
HKI-272 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for HKI-272. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of HKI-272 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [284]
Indium-111 [Phase 2/3]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Indium-111. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Indium-111 through regulating the expression of Epidermal growth factor receptor (EGFR). [90], [265]
Rindopepimut [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Rindopepimut. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Rindopepimut through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [285]
SYM-004 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for SYM-004. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SYM-004 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [286]
Varlitinib [Phase 2/3]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Varlitinib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Varlitinib through regulating the expression of Epidermal growth factor receptor (EGFR). [7], [265]
Zalutumumab [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Zalutumumab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Zalutumumab through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [268]
ABT-414 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for ABT-414. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ABT-414 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [267]
ABX-EGF [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for ABX-EGF. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ABX-EGF through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [287]
AFM24 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for AFM24. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AFM24 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [288]
ASP8273 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for ASP8273. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ASP8273 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [289]
BDTX-189 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for BDTX-189. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BDTX-189 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [290]
BMS-599626 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for BMS-599626. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BMS-599626 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [266]
BMS-690514 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for BMS-690514. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BMS-690514 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [285]
CART-EGFR [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for CART-EGFR. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CART-EGFR through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [291]
CetuGEX [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for CetuGEX. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CetuGEX through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [292]
CI-1033 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for CI-1033. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CI-1033 through regulating the expression of Epidermal growth factor receptor (EGFR). [15], [265]
CK-101 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for CK-101. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CK-101 through regulating the expression of Epidermal growth factor receptor (EGFR). [15], [265]
Depatuxizumab [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Depatuxizumab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Depatuxizumab through regulating the expression of Epidermal growth factor receptor (EGFR). [15], [265]
EGFR antisense DNA [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for EGFR antisense DNA. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of EGFR antisense DNA through regulating the expression of Epidermal growth factor receptor (EGFR). [15], [265]
EGFR CART [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for EGFR CART. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of EGFR CART through regulating the expression of Epidermal growth factor receptor (EGFR). [41], [265]
EMB-01 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for EMB-01. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of EMB-01 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [293]
EMD 55900 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for EMD 55900. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of EMD 55900 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [294]
HER1-VSSP vaccine [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for HER1-VSSP vaccine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of HER1-VSSP vaccine through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [295]
HM-78136B [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for HM-78136B. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of HM-78136B through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [296]
Matuzumab [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Matuzumab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Matuzumab through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [297]
MEHD-7945A [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for MEHD-7945A. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MEHD-7945A through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [298]
Pelitinib [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Pelitinib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Pelitinib through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [299]
RM-1929 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for RM-1929. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of RM-1929 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [300]
SN-32793 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for SN-32793. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SN-32793 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [301]
Sym013 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Sym013. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Sym013 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [302]
Sym015 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Sym015. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Sym015 through regulating the expression of Epidermal growth factor receptor (EGFR). [41], [265]
Tarloxotinib [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Tarloxotinib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Tarloxotinib through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [303]
TT-100 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for TT-100. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of TT-100 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [304]
VATALANIB [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for VATALANIB. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of VATALANIB through regulating the expression of Epidermal growth factor receptor (EGFR). [90], [265]
ZN-e4 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for ZN-e4. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ZN-e4 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [305]
AMG 595 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for AMG 595. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AMG 595 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [306]
Anti-EGFR CAR T [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Anti-EGFR CAR T. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Anti-EGFR CAR T through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [307]
AP32788 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for AP32788. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AP32788 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [308]
AST-1306 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for AST-1306. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AST-1306 through regulating the expression of Epidermal growth factor receptor (EGFR). [90], [265]
BCA101 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for BCA101. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BCA101 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [309]
BIBX-1382 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for BIBX-1382. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BIBX-1382 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [310]
Cipatinib [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Cipatinib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cipatinib through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [311]
CLN-081 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for CLN-081. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CLN-081 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [312]
CUDC-101 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for CUDC-101. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CUDC-101 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [313]
D2C7 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for D2C7. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of D2C7 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [314]
EGFR806-specific CAR T cell [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for EGFR806-specific CAR T cell. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of EGFR806-specific CAR T cell through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [315]
IMGN289 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for IMGN289. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of IMGN289 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
JNJ-26483327 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for JNJ-26483327. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of JNJ-26483327 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [316]
LY3164530 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for LY3164530. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LY3164530 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [317]
MCLA-158 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for MCLA-158. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MCLA-158 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [318]
MM-151 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for MM-151. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MM-151 through regulating the expression of Epidermal growth factor receptor (EGFR). [15], [265]
MR1-1 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for MR1-1. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MR1-1 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [319]
PF-05230907 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for PF-05230907. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PF-05230907 through regulating the expression of Epidermal growth factor receptor (EGFR). [41], [265]
Pyrotinib [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Pyrotinib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Pyrotinib through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [320]
S-222611 [Phase 1b]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for S-222611. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of S-222611 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
SI-B001 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for SI-B001. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SI-B001 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [321]
SYN004 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for SYN004. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SYN004 through regulating the expression of Epidermal growth factor receptor (EGFR). [41], [265]
111In-hEGF [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 111In-hEGF. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 111In-hEGF through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [322]
(3-Bromo-phenyl)-(5-nitro-quinazolin-4-yl)-amine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for (3-Bromo-phenyl)-(5-nitro-quinazolin-4-yl)-amine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of (3-Bromo-phenyl)-(5-nitro-quinazolin-4-yl)-amine through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [323]
(3-Bromo-phenyl)-quinazolin-4-yl-amine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for (3-Bromo-phenyl)-quinazolin-4-yl-amine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of (3-Bromo-phenyl)-quinazolin-4-yl-amine through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [324]
(E)-5-(4-Hydroxybenzylidene)-1-phenethylhydantoin [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for (E)-5-(4-Hydroxybenzylidene)-1-phenethylhydantoin. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of (E)-5-(4-Hydroxybenzylidene)-1-phenethylhydantoin through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [325]
(S)-benzyl 4-chloro-3-oxobutan-2-ylcarbamate [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for (S)-benzyl 4-chloro-3-oxobutan-2-ylcarbamate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of (S)-benzyl 4-chloro-3-oxobutan-2-ylcarbamate through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [323]
10-hydroxy-18-methoxybetaenone [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 10-hydroxy-18-methoxybetaenone. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 10-hydroxy-18-methoxybetaenone through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [323]
2-(4,5-Dihydroxy-indan-1-ylidene)-malononitrile [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 2-(4,5-Dihydroxy-indan-1-ylidene)-malononitrile. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 2-(4,5-Dihydroxy-indan-1-ylidene)-malononitrile through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [326]
2-(5,6-Dihydroxy-indan-1-ylidene)-malononitrile [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 2-(5,6-Dihydroxy-indan-1-ylidene)-malononitrile. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 2-(5,6-Dihydroxy-indan-1-ylidene)-malononitrile through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [327]
2-benzoyl-3-(3,4-dihydroxyphenyl)acrylonitrile [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 2-benzoyl-3-(3,4-dihydroxyphenyl)acrylonitrile. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 2-benzoyl-3-(3,4-dihydroxyphenyl)acrylonitrile through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [323]
2-cyano-3-(3,4-dihydroxyphenyl)acrylamide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 2-cyano-3-(3,4-dihydroxyphenyl)acrylamide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 2-cyano-3-(3,4-dihydroxyphenyl)acrylamide through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [323]
2-methoxy-4-(2-nitrovinyl)phenol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 2-methoxy-4-(2-nitrovinyl)phenol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 2-methoxy-4-(2-nitrovinyl)phenol through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [323]
3,4-di-(4-methoxyphenyl)-1H-pyrrole-2,5-dione [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 3,4-di-(4-methoxyphenyl)-1H-pyrrole-2,5-dione. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 3,4-di-(4-methoxyphenyl)-1H-pyrrole-2,5-dione through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [328]
3,4-diphenyl-1H-pyrrole-2,5-dione [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 3,4-diphenyl-1H-pyrrole-2,5-dione. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 3,4-diphenyl-1H-pyrrole-2,5-dione through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [329]
3-(3-Chloro-phenyl)-5,7-dihydroxy-chromen-4-one [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 3-(3-Chloro-phenyl)-5,7-dihydroxy-chromen-4-one. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 3-(3-Chloro-phenyl)-5,7-dihydroxy-chromen-4-one through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [330]
3-(4-methoxyphenyl)-4-phenyl-1H-pyrrole-2,5-dione [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 3-(4-methoxyphenyl)-4-phenyl-1H-pyrrole-2,5-dione. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 3-(4-methoxyphenyl)-4-phenyl-1H-pyrrole-2,5-dione through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [331]
3-(indole-3-yl)-4-phenyl-1H-pyrrole-2,5-dione [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 3-(indole-3-yl)-4-phenyl-1H-pyrrole-2,5-dione. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 3-(indole-3-yl)-4-phenyl-1H-pyrrole-2,5-dione through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [332]
3-Pyridin-4-yl-quinoline-6,7-diol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 3-Pyridin-4-yl-quinoline-6,7-diol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 3-Pyridin-4-yl-quinoline-6,7-diol through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [333]
4-(2-nitroprop-1-enyl)benzene-1,2-diol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 4-(2-nitroprop-1-enyl)benzene-1,2-diol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 4-(2-nitroprop-1-enyl)benzene-1,2-diol through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [323]
4-(2-nitrovinyl)benzene-1,2-diol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 4-(2-nitrovinyl)benzene-1,2-diol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 4-(2-nitrovinyl)benzene-1,2-diol through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [334]
4-(2-nitrovinyl)phenol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 4-(2-nitrovinyl)phenol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 4-(2-nitrovinyl)phenol through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [323]
4-(3-Bromo-phenoxy)-6,7-dimethoxy-quinazoline [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 4-(3-Bromo-phenoxy)-6,7-dimethoxy-quinazoline. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 4-(3-Bromo-phenoxy)-6,7-dimethoxy-quinazoline through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [335]
4-(3-Bromo-phenoxy)-6,7-dimethoxy-quinoline [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 4-(3-Bromo-phenoxy)-6,7-dimethoxy-quinoline. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 4-(3-Bromo-phenoxy)-6,7-dimethoxy-quinoline through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [324]
4-(4-(2-nitrovinyl)phenoxysulfonyl)benzoic acid [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 4-(4-(2-nitrovinyl)phenoxysulfonyl)benzoic acid. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 4-(4-(2-nitrovinyl)phenoxysulfonyl)benzoic acid through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [323]
4-(5-Bromoindole-3-yl)-6,7-dimethoxyquinazoline [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 4-(5-Bromoindole-3-yl)-6,7-dimethoxyquinazoline. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 4-(5-Bromoindole-3-yl)-6,7-dimethoxyquinazoline through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [336]
4-acrylamido-N-(3-bromophenyl)-2-hydroxybenzamide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 4-acrylamido-N-(3-bromophenyl)-2-hydroxybenzamide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 4-acrylamido-N-(3-bromophenyl)-2-hydroxybenzamide through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [337]
4-biphenyl-2-ylethynyl-6,7-dimethoxy-quinazoline [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 4-biphenyl-2-ylethynyl-6,7-dimethoxy-quinazoline. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 4-biphenyl-2-ylethynyl-6,7-dimethoxy-quinazoline through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [338]
4557W [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 4557W. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 4557W through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [339]
5,6-Bis-p-tolylamino-isoindole-1,3-dione [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 5,6-Bis-p-tolylamino-isoindole-1,3-dione. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 5,6-Bis-p-tolylamino-isoindole-1,3-dione through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [340]
5-acrylamido-N-(3-bromophenyl)-2-hydroxybenzamide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 5-acrylamido-N-(3-bromophenyl)-2-hydroxybenzamide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 5-acrylamido-N-(3-bromophenyl)-2-hydroxybenzamide through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [341]
6,7-diethoxy-4-(4-phenylbut-1-enyl)quinazoline [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 6,7-diethoxy-4-(4-phenylbut-1-enyl)quinazoline. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 6,7-diethoxy-4-(4-phenylbut-1-enyl)quinazoline through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [338]
6,7-diethoxy-4-(5-phenylpent-1-enyl)quinazoline [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 6,7-diethoxy-4-(5-phenylpent-1-enyl)quinazoline. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 6,7-diethoxy-4-(5-phenylpent-1-enyl)quinazoline through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [338]
6,7-diethoxy-4-styrylquinazoline [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 6,7-diethoxy-4-styrylquinazoline. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 6,7-diethoxy-4-styrylquinazoline through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [338]
6,7-dimethoxy-4-(2-phenylethynyl)quinazoline [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 6,7-dimethoxy-4-(2-phenylethynyl)quinazoline. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 6,7-dimethoxy-4-(2-phenylethynyl)quinazoline through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [338]
6,7-dimethoxy-4-(3-phenoxyprop-1-ynyl)quinazoline [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 6,7-dimethoxy-4-(3-phenoxyprop-1-ynyl)quinazoline. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 6,7-dimethoxy-4-(3-phenoxyprop-1-ynyl)quinazoline through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [338]
6,7-dimethoxy-4-(4-phenylbut-1-ynyl)quinazoline [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 6,7-dimethoxy-4-(4-phenylbut-1-ynyl)quinazoline. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 6,7-dimethoxy-4-(4-phenylbut-1-ynyl)quinazoline through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [342]
6,7-dimethoxy-N-m-tolylquinazolin-4-amine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 6,7-dimethoxy-N-m-tolylquinazolin-4-amine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 6,7-dimethoxy-N-m-tolylquinazolin-4-amine through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [331]
6-chloro-N-(3-chlorophenyl)quinazolin-4-amine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for 6-chloro-N-(3-chlorophenyl)quinazolin-4-amine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 6-chloro-N-(3-chlorophenyl)quinazolin-4-amine through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [331]
AFM-21 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for AFM-21. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AFM-21 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
AG 112 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for AG 112. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AG 112 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [343]
AG 9 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for AG 9. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AG 9 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
AG-213 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for AG-213. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AG-213 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [323]
AG-538 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for AG-538. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AG-538 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [344]
AG1478 [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for AG1478. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AG1478 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [345]
AGT-2000 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for AGT-2000. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AGT-2000 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
AL-6802 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for AL-6802. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AL-6802 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
Anti-EGFR humanized mabs [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Anti-EGFR humanized mabs. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Anti-EGFR humanized mabs through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
Anti-EGFR mab [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Anti-EGFR mab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Anti-EGFR mab through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
ARX-AHD [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for ARX-AHD. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ARX-AHD through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
Benzo[g]quinazolin-4-yl-(3-bromo-phenyl)-amine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Benzo[g]quinazolin-4-yl-(3-bromo-phenyl)-amine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Benzo[g]quinazolin-4-yl-(3-bromo-phenyl)-amine through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [335]
Benzyl-quinazolin-4-yl-amine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Benzyl-quinazolin-4-yl-amine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Benzyl-quinazolin-4-yl-amine through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [336]
Bmab-200 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Bmab-200. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Bmab-200 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
BPIQ-I [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for BPIQ-I. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BPIQ-I through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [346]
CL-387785 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for CL-387785. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CL-387785 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [337]
Cochliobolic acid [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Cochliobolic acid. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cochliobolic acid through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [347]
EDP-13 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for EDP-13. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of EDP-13 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
EGFR inhibitor [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for EGFR inhibitor. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of EGFR inhibitor through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [348]
Epitinib [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Epitinib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Epitinib through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
FHT-2107 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for FHT-2107. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of FHT-2107 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
GI-3000 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for GI-3000. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of GI-3000 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
HDS-029 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for HDS-029. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of HDS-029 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [349]
HKI-9924129 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for HKI-9924129. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of HKI-9924129 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [350]
HM-61713B [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for HM-61713B. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of HM-61713B through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
HTS-00213 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for HTS-00213. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of HTS-00213 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [331]
HTS-02876 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for HTS-02876. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of HTS-02876 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [351]
HTS-05058 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for HTS-05058. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of HTS-05058 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [328]
ICR 62 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for ICR 62. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ICR 62 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [352]
IPS-01003 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for IPS-01003. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of IPS-01003 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
LA22-radioimmunoconjugates [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for LA22-radioimmunoconjugates. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LA22-radioimmunoconjugates through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
LAVENDUSTIN A [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for LAVENDUSTIN A. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LAVENDUSTIN A through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [338]
mabionHER2 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for mabionHER2. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of mabionHER2 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
MDP-01 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for MDP-01. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MDP-01 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
MG-111 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for MG-111. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MG-111 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [353]
MT-062 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for MT-062. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MT-062 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
N*4*-(3-Bromo-phenyl)-quinazoline-4,6,7-triamine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for N*4*-(3-Bromo-phenyl)-quinazoline-4,6,7-triamine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N*4*-(3-Bromo-phenyl)-quinazoline-4,6,7-triamine through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [354]
N*4*-(3-Bromo-phenyl)-quinazoline-4,6-diamine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for N*4*-(3-Bromo-phenyl)-quinazoline-4,6-diamine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N*4*-(3-Bromo-phenyl)-quinazoline-4,6-diamine through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [355]
N*4*-(3-Bromo-phenyl)-quinazoline-4,7-diamine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for N*4*-(3-Bromo-phenyl)-quinazoline-4,7-diamine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N*4*-(3-Bromo-phenyl)-quinazoline-4,7-diamine through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [356]
N*4*-Benzyl-pyrido[4,3-d]pyrimidine-4,7-diamine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for N*4*-Benzyl-pyrido[4,3-d]pyrimidine-4,7-diamine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N*4*-Benzyl-pyrido[4,3-d]pyrimidine-4,7-diamine through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [344]
N-(4-(phenylamino)quinazolin-6-yl)acrylamide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for N-(4-(phenylamino)quinazolin-6-yl)acrylamide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-(4-(phenylamino)quinazolin-6-yl)acrylamide through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [352]
N-(4-m-Tolylamino-quinazolin-6-yl)-acrylamide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for N-(4-m-Tolylamino-quinazolin-6-yl)-acrylamide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-(4-m-Tolylamino-quinazolin-6-yl)-acrylamide through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [326]
N-(4-m-Tolylamino-quinazolin-7-yl)-acrylamide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for N-(4-m-Tolylamino-quinazolin-7-yl)-acrylamide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-(4-m-Tolylamino-quinazolin-7-yl)-acrylamide through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [324]
N4-(3-chlorophenyl)quinazoline-4,6-diamine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for N4-(3-chlorophenyl)quinazoline-4,6-diamine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N4-(3-chlorophenyl)quinazoline-4,6-diamine through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [354]
N4-(3-methylphenyl)-4,6-quinazolinediamine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for N4-(3-methylphenyl)-4,6-quinazolinediamine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N4-(3-methylphenyl)-4,6-quinazolinediamine through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [328]
NRC-2694 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for NRC-2694. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of NRC-2694 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
ON-128 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for ON-128. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ON-128 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [324]
OSI-75 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for OSI-75. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of OSI-75 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [357]
PD-0166326 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for PD-0166326. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PD-0166326 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [325]
PD-0173956 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for PD-0173956. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PD-0173956 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [325]
PD-158780 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for PD-158780. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PD-158780 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [324]
PD-168393 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for PD-168393. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PD-168393 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [356]
PD182905 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for PD182905. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PD182905 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [301]
PF 5208766 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for PF 5208766. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PF 5208766 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [358]
PP121 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for PP121. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PP121 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [359]
RG-50810 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for RG-50810. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of RG-50810 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [351]
RM-6427 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for RM-6427. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of RM-6427 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
Ro-4396686 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Ro-4396686. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ro-4396686 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [328]
RX-1792 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for RX-1792. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of RX-1792 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
SYM-011 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for SYM-011. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SYM-011 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
TGF alpha [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for TGF alpha. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of TGF alpha through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
Theliatinib [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Theliatinib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Theliatinib through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [360]
WHI-P154 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for WHI-P154. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of WHI-P154 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [342]
WZ-3146 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for WZ-3146. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of WZ-3146 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [277]
AZD-9935 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for AZD-9935. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AZD-9935 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [361]
AZD4769 [Discontinued in Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for AZD4769. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AZD4769 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [266]
CGP-52411 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for CGP-52411. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CGP-52411 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [362]
CGP-53353 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for CGP-53353. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CGP-53353 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [301]
Heparin-EGF-like factor [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for Heparin-EGF-like factor. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Heparin-EGF-like factor through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [363]
PD-153035 [Discontinued in Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for PD-153035. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PD-153035 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [364]
PKI166 [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for PKI166. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PKI166 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [365]
RG7160 [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for RG7160. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of RG7160 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [366]
TAK165 [Discontinued in Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Epidermal growth factor receptor (EGFR) is a therapeutic target for TAK165. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of TAK165 through regulating the expression of Epidermal growth factor receptor (EGFR). [265], [367]
Fascin (FSCN1)
NP-G2-044 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Fascin (FSCN1) is a therapeutic target for NP-G2-044. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of NP-G2-044 through regulating the expression of Fascin (FSCN1). [368], [369]
Fibroblast growth factor receptor 4 (FGFR4)
FGF401 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Fibroblast growth factor receptor 4 (FGFR4) is a therapeutic target for FGF401. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of FGF401 through regulating the expression of Fibroblast growth factor receptor 4 (FGFR4). [15], [34]
INCB62079 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Fibroblast growth factor receptor 4 (FGFR4) is a therapeutic target for INCB62079. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of INCB62079 through regulating the expression of Fibroblast growth factor receptor 4 (FGFR4). [34], [370]
ISIS-FGFR4 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Fibroblast growth factor receptor 4 (FGFR4) is a therapeutic target for ISIS-FGFR4. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS-FGFR4 through regulating the expression of Fibroblast growth factor receptor 4 (FGFR4). [34], [332]
BLU-554 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Fibroblast growth factor receptor 4 (FGFR4) is a therapeutic target for BLU-554. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BLU-554 through regulating the expression of Fibroblast growth factor receptor 4 (FGFR4). [15], [34]
H3B-6527 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Fibroblast growth factor receptor 4 (FGFR4) is a therapeutic target for H3B-6527. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of H3B-6527 through regulating the expression of Fibroblast growth factor receptor 4 (FGFR4). [15], [34]
ABC-4 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Fibroblast growth factor receptor 4 (FGFR4) is a therapeutic target for ABC-4. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ABC-4 through regulating the expression of Fibroblast growth factor receptor 4 (FGFR4). [34], [371]
ACTB-1003 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Fibroblast growth factor receptor 4 (FGFR4) is a therapeutic target for ACTB-1003. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ACTB-1003 through regulating the expression of Fibroblast growth factor receptor 4 (FGFR4). [15], [34]
Ro-4396686 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Fibroblast growth factor receptor 4 (FGFR4) is a therapeutic target for Ro-4396686. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ro-4396686 through regulating the expression of Fibroblast growth factor receptor 4 (FGFR4). [34], [372]
PD-0183812 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Fibroblast growth factor receptor 4 (FGFR4) is a therapeutic target for PD-0183812. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PD-0183812 through regulating the expression of Fibroblast growth factor receptor 4 (FGFR4). [15], [34]
Forkhead box protein O1A (FOXO1)
AS-1708727 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Forkhead box protein O1A (FOXO1) is a therapeutic target for AS-1708727. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AS-1708727 through regulating the expression of Forkhead box protein O1A (FOXO1). [373], [374]
ISIS 188755 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Forkhead box protein O1A (FOXO1) is a therapeutic target for ISIS 188755. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 188755 through regulating the expression of Forkhead box protein O1A (FOXO1). [373], [375]
ISIS 188757 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Forkhead box protein O1A (FOXO1) is a therapeutic target for ISIS 188757. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 188757 through regulating the expression of Forkhead box protein O1A (FOXO1). [373], [375]
ISIS 188759 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Forkhead box protein O1A (FOXO1) is a therapeutic target for ISIS 188759. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 188759 through regulating the expression of Forkhead box protein O1A (FOXO1). [373], [375]
ISIS 188761 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Forkhead box protein O1A (FOXO1) is a therapeutic target for ISIS 188761. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 188761 through regulating the expression of Forkhead box protein O1A (FOXO1). [373], [375]
ISIS 188763 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Forkhead box protein O1A (FOXO1) is a therapeutic target for ISIS 188763. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 188763 through regulating the expression of Forkhead box protein O1A (FOXO1). [373], [375]
ISIS 188778 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Forkhead box protein O1A (FOXO1) is a therapeutic target for ISIS 188778. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 188778 through regulating the expression of Forkhead box protein O1A (FOXO1). [373], [375]
ISIS 188780 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Forkhead box protein O1A (FOXO1) is a therapeutic target for ISIS 188780. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 188780 through regulating the expression of Forkhead box protein O1A (FOXO1). [373], [375]
ISIS 188781 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Forkhead box protein O1A (FOXO1) is a therapeutic target for ISIS 188781. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 188781 through regulating the expression of Forkhead box protein O1A (FOXO1). [373], [375]
ISIS 188782 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Forkhead box protein O1A (FOXO1) is a therapeutic target for ISIS 188782. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 188782 through regulating the expression of Forkhead box protein O1A (FOXO1). [373], [376]
Glycogen synthase kinase-3 beta (GSK-3B)
AMO-02 [Phase 2/3]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for AMO-02. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AMO-02 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [377]
9-ING-41 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for 9-ING-41. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 9-ING-41 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [378]
Lithium [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for Lithium. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Lithium through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [379]
LY2090314 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for LY2090314. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LY2090314 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [380]
Neu-120 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for Neu-120. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Neu-120 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [381]
Tideglusib [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for Tideglusib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Tideglusib through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [382]
(E)-N-(6-(prop-1-enyl)-1H-indazol-3-yl)butyramide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for (E)-N-(6-(prop-1-enyl)-1H-indazol-3-yl)butyramide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of (E)-N-(6-(prop-1-enyl)-1H-indazol-3-yl)butyramide through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [383]
12,13-DEHYDRO-8-O-ACETYLMANZAMINE A [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for 12,13-DEHYDRO-8-O-ACETYLMANZAMINE A. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 12,13-DEHYDRO-8-O-ACETYLMANZAMINE A through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [384]
12,13-DEHYDROMANZAMINE A [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for 12,13-DEHYDROMANZAMINE A. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 12,13-DEHYDROMANZAMINE A through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [384]
3-(6-(phenylamino)-9H-purin-8-yl)benzonitrile [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for 3-(6-(phenylamino)-9H-purin-8-yl)benzonitrile. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 3-(6-(phenylamino)-9H-purin-8-yl)benzonitrile through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [385]
3-phenyl-4-(phenylamino)-1H-pyrrole-2,5-dione [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for 3-phenyl-4-(phenylamino)-1H-pyrrole-2,5-dione. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 3-phenyl-4-(phenylamino)-1H-pyrrole-2,5-dione through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [386]
4,5,6,7-tetrabromo-1H-benzo[d][1,2,3]triazole [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for 4,5,6,7-tetrabromo-1H-benzo[d][1,2,3]triazole. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 4,5,6,7-tetrabromo-1H-benzo[d][1,2,3]triazole through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [387]
4-(5-bromo-1H-indol-3-yl)pyrimidin-2-amine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for 4-(5-bromo-1H-indol-3-yl)pyrimidin-2-amine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 4-(5-bromo-1H-indol-3-yl)pyrimidin-2-amine through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [369]
6-deoxymanzamine X [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for 6-deoxymanzamine X. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 6-deoxymanzamine X through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [384]
8-O-(4-bromobenzenesulfonyl)manzamine F [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for 8-O-(4-bromobenzenesulfonyl)manzamine F. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 8-O-(4-bromobenzenesulfonyl)manzamine F through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [384]
8-O-(4-chlorobenzenesulfonyl)manzamine F [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for 8-O-(4-chlorobenzenesulfonyl)manzamine F. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 8-O-(4-chlorobenzenesulfonyl)manzamine F through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [388]
8-O-(4-toluenesulfonyl)manzamine A [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for 8-O-(4-toluenesulfonyl)manzamine A. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 8-O-(4-toluenesulfonyl)manzamine A through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [388]
8-OH-MANZAMINE A [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for 8-OH-MANZAMINE A. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 8-OH-MANZAMINE A through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [389]
9-N-ETHYL-8-ETHOXY-MANZAMINE A [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for 9-N-ETHYL-8-ETHOXY-MANZAMINE A. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 9-N-ETHYL-8-ETHOXY-MANZAMINE A through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [384]
9-N-METHYL-8-METHOXY-MANZAMINE A [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for 9-N-METHYL-8-METHOXY-MANZAMINE A. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 9-N-METHYL-8-METHOXY-MANZAMINE A through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [384]
alsterpaullone 2-cyanoethyl [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for alsterpaullone 2-cyanoethyl. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of alsterpaullone 2-cyanoethyl through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [390]
AMP-PNP [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for AMP-PNP. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AMP-PNP through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [391]
AS-601245 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for AS-601245. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AS-601245 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [392]
AZAKENPAULLONE [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for AZAKENPAULLONE. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AZAKENPAULLONE through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [393]
Bisindolylmaleimide-I [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for Bisindolylmaleimide-I. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Bisindolylmaleimide-I through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [393]
BX-795 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for BX-795. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BX-795 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [390]
BX-912 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for BX-912. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BX-912 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [342]
CHIR-98014 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for CHIR-98014. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CHIR-98014 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [394]
CHIR-98023 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for CHIR-98023. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CHIR-98023 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [395]
CI-1040 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for CI-1040. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CI-1040 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [396]
CP-70949 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for CP-70949. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CP-70949 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [397]
CT-98024 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for CT-98024. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CT-98024 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [398]
DM-204 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for DM-204. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of DM-204 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [378]
ELLAGIC ACID [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for ELLAGIC ACID. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ELLAGIC ACID through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [385]
GSK-3beta inhibitor II [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for GSK-3beta inhibitor II. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of GSK-3beta inhibitor II through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [399]
GSK-3beta inhibitor XI [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for GSK-3beta inhibitor XI. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of GSK-3beta inhibitor XI through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [400]
I-5 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for I-5. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of I-5 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [96]
IM-12 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for IM-12. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of IM-12 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [401]
indirubin deriv. 8a [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for indirubin deriv. 8a. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of indirubin deriv. 8a through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [402]
K00244 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for K00244. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of K00244 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [403]
L-779450 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for L-779450. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of L-779450 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [404]
LEUCETTAMINE B [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for LEUCETTAMINE B. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LEUCETTAMINE B through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [405]
MANZAMINE A [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for MANZAMINE A. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MANZAMINE A through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [384]
Manzamine E [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for Manzamine E. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Manzamine E through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [384]
Manzamine Y [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for Manzamine Y. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Manzamine Y through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [388]
N,8-diphenyl-9H-purin-6-amine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for N,8-diphenyl-9H-purin-6-amine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N,8-diphenyl-9H-purin-6-amine through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [388]
N-(6-(2-chlorophenyl)-1H-indazol-3-yl)butyramide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for N-(6-(2-chlorophenyl)-1H-indazol-3-yl)butyramide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-(6-(2-chlorophenyl)-1H-indazol-3-yl)butyramide through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [395]
N-(6-(3-hydroxyphenyl)-1H-indazol-3-yl)butyramide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for N-(6-(3-hydroxyphenyl)-1H-indazol-3-yl)butyramide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-(6-(3-hydroxyphenyl)-1H-indazol-3-yl)butyramide through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [395]
N-(6-(4-aminophenyl)-1H-indazol-3-yl)butyramide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for N-(6-(4-aminophenyl)-1H-indazol-3-yl)butyramide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-(6-(4-aminophenyl)-1H-indazol-3-yl)butyramide through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [395]
N-(6-(4-fluorophenyl)-1H-indazol-3-yl)butyramide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for N-(6-(4-fluorophenyl)-1H-indazol-3-yl)butyramide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-(6-(4-fluorophenyl)-1H-indazol-3-yl)butyramide through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [395]
N-(6-(4-hydroxyphenyl)-1H-indazol-3-yl)butyramide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for N-(6-(4-hydroxyphenyl)-1H-indazol-3-yl)butyramide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-(6-(4-hydroxyphenyl)-1H-indazol-3-yl)butyramide through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [395]
N-(6-(furan-3-yl)-1H-indazol-3-yl)butyramide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for N-(6-(furan-3-yl)-1H-indazol-3-yl)butyramide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-(6-(furan-3-yl)-1H-indazol-3-yl)butyramide through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [395]
N-(6-(pyridin-3-yl)-1H-indazol-3-yl)butyramide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for N-(6-(pyridin-3-yl)-1H-indazol-3-yl)butyramide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-(6-(pyridin-3-yl)-1H-indazol-3-yl)butyramide through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [406]
N-(6-(pyridin-4-yl)-1H-indazol-3-yl)butyramide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for N-(6-(pyridin-4-yl)-1H-indazol-3-yl)butyramide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-(6-(pyridin-4-yl)-1H-indazol-3-yl)butyramide through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [405]
N-(6-(thiophen-3-yl)-1H-indazol-3-yl)butyramide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for N-(6-(thiophen-3-yl)-1H-indazol-3-yl)butyramide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-(6-(thiophen-3-yl)-1H-indazol-3-yl)butyramide through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [383]
N-(6-(trifluoromethyl)-1H-indazol-3-yl)butyramide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for N-(6-(trifluoromethyl)-1H-indazol-3-yl)butyramide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-(6-(trifluoromethyl)-1H-indazol-3-yl)butyramide through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [395]
N-(6-benzyl-1H-indazol-3-yl)butyramide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for N-(6-benzyl-1H-indazol-3-yl)butyramide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-(6-benzyl-1H-indazol-3-yl)butyramide through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [395]
N-(6-bromo-1H-indazol-3-yl)butyramide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for N-(6-bromo-1H-indazol-3-yl)butyramide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-(6-bromo-1H-indazol-3-yl)butyramide through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [395]
N-(6-chloro-1H-indazol-3-yl)butyramide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for N-(6-chloro-1H-indazol-3-yl)butyramide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-(6-chloro-1H-indazol-3-yl)butyramide through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [395]
N-(6-chloro-5-p-tolyl-1H-indazol-3-yl)butyramide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for N-(6-chloro-5-p-tolyl-1H-indazol-3-yl)butyramide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-(6-chloro-5-p-tolyl-1H-indazol-3-yl)butyramide through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [395]
N-(6-chloro-5-phenyl-1H-indazol-3-yl)butyramide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for N-(6-chloro-5-phenyl-1H-indazol-3-yl)butyramide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-(6-chloro-5-phenyl-1H-indazol-3-yl)butyramide through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [395]
N-(6-phenethyl-1H-indazol-3-yl)butyramide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for N-(6-phenethyl-1H-indazol-3-yl)butyramide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-(6-phenethyl-1H-indazol-3-yl)butyramide through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [383]
N-(6-phenyl-1H-indazol-3-yl)butyramide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for N-(6-phenyl-1H-indazol-3-yl)butyramide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-(6-phenyl-1H-indazol-3-yl)butyramide through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [395]
N-(8-(3-cyanophenyl)-9H-purin-6-yl)pentanamide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for N-(8-(3-cyanophenyl)-9H-purin-6-yl)pentanamide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-(8-(3-cyanophenyl)-9H-purin-6-yl)pentanamide through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [385]
Neo-kauluamine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for Neo-kauluamine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Neo-kauluamine through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [407]
NU-6102 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for NU-6102. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of NU-6102 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [408]
PAULLONE [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for PAULLONE. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PAULLONE through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [377]
PF-228 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for PF-228. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PF-228 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [395]
PYRAZOLOPYRIDAZINE 1 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for PYRAZOLOPYRIDAZINE 1. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PYRAZOLOPYRIDAZINE 1 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [391]
PYRAZOLOPYRIDAZINE 2 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for PYRAZOLOPYRIDAZINE 2. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PYRAZOLOPYRIDAZINE 2 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [405]
Quinoxaline1 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for Quinoxaline1. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Quinoxaline1 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [409]
RGB-286147 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for RGB-286147. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of RGB-286147 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [342]
Ro31-8220 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for Ro31-8220. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ro31-8220 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [410]
SB-415286 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for SB-415286. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SB-415286 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [369]
STAUROSPORINONE [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for STAUROSPORINONE. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of STAUROSPORINONE through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [411]
Thieno analogue of kenpaullone [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for Thieno analogue of kenpaullone. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Thieno analogue of kenpaullone through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [412]
TWS-119 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for TWS-119. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of TWS-119 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [413]
AZD-1080 [Discontinued in Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for AZD-1080. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AZD-1080 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [414]
RO-320432 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for RO-320432. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of RO-320432 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [415]
SAN-61 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Glycogen synthase kinase-3 beta (GSK-3B) is a therapeutic target for SAN-61. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SAN-61 through regulating the expression of Glycogen synthase kinase-3 beta (GSK-3B). [34], [416]
Insulin-like growth factor-I (IGF1)
Xentuzumab [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor-I (IGF1) is a therapeutic target for Xentuzumab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Xentuzumab through regulating the expression of Insulin-like growth factor-I (IGF1). [417], [418]
BI-836845 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor-I (IGF1) is a therapeutic target for BI-836845. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BI-836845 through regulating the expression of Insulin-like growth factor-I (IGF1). [41], [417]
MEDI-573 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor-I (IGF1) is a therapeutic target for MEDI-573. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MEDI-573 through regulating the expression of Insulin-like growth factor-I (IGF1). [417], [419]
Interferon-beta (IFNB1)
Interferon beta-1a [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Interferon-beta (IFNB1) is a therapeutic target for Interferon beta-1a. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Interferon beta-1a through regulating the expression of Interferon-beta (IFNB1). [420], [421]
PEGylated IFN beta 1-a [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Interferon-beta (IFNB1) is a therapeutic target for PEGylated IFN beta 1-a. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PEGylated IFN beta 1-a through regulating the expression of Interferon-beta (IFNB1). [420], [422]
PLEGRIDY [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Interferon-beta (IFNB1) is a therapeutic target for PLEGRIDY. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PLEGRIDY through regulating the expression of Interferon-beta (IFNB1). [420], [423]
Biferonex [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Interferon-beta (IFNB1) is a therapeutic target for Biferonex. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Biferonex through regulating the expression of Interferon-beta (IFNB1). [420], [424]
FP-1201 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Interferon-beta (IFNB1) is a therapeutic target for FP-1201. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of FP-1201 through regulating the expression of Interferon-beta (IFNB1). [420], [425]
NU-100 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Interferon-beta (IFNB1) is a therapeutic target for NU-100. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of NU-100 through regulating the expression of Interferon-beta (IFNB1). [420], [426]
AZ-01, PEGylated interferon-beta [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Interferon-beta (IFNB1) is a therapeutic target for AZ-01, PEGylated interferon-beta. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AZ-01, PEGylated interferon-beta through regulating the expression of Interferon-beta (IFNB1). [90], [420]
Interferon beta 1a [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Interferon-beta (IFNB1) is a therapeutic target for Interferon beta 1a. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Interferon beta 1a through regulating the expression of Interferon-beta (IFNB1). [420], [427]
PF-06823859 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Interferon-beta (IFNB1) is a therapeutic target for PF-06823859. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PF-06823859 through regulating the expression of Interferon-beta (IFNB1). [420], [427]
ARX-424 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Interferon-beta (IFNB1) is a therapeutic target for ARX-424. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ARX-424 through regulating the expression of Interferon-beta (IFNB1). [420], [428]
Gene therapy, IFN-b [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Interferon-beta (IFNB1) is a therapeutic target for Gene therapy, IFN-b. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Gene therapy, IFN-b through regulating the expression of Interferon-beta (IFNB1). [39], [420]
TV-1390 [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Interferon-beta (IFNB1) is a therapeutic target for TV-1390. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of TV-1390 through regulating the expression of Interferon-beta (IFNB1). [420], [427]
Maxy-10 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Interferon-beta (IFNB1) is a therapeutic target for Maxy-10. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Maxy-10 through regulating the expression of Interferon-beta (IFNB1). [420], [429]
Interferon-gamma (IFNG)
Emapalumab [Approved]
In total 2 mechanisms lead to this potential drug response
Response Summary Interferon-gamma (IFNG) is a therapeutic target for Emapalumab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Emapalumab through regulating the expression of Interferon-gamma (IFNG). [65], [430]
Interferon-gamma (IFNG) is a therapeutic target for Emapalumab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Emapalumab through regulating the expression of Interferon-gamma (IFNG). [65], [369]
Fumaric acid [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Interferon-gamma (IFNG) is a therapeutic target for Fumaric acid. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Fumaric acid through regulating the expression of Interferon-gamma (IFNG). [65], [431]
VIR-201 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Interferon-gamma (IFNG) is a therapeutic target for VIR-201. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of VIR-201 through regulating the expression of Interferon-gamma (IFNG). [65], [432]
AMG 811 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Interferon-gamma (IFNG) is a therapeutic target for AMG 811. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AMG 811 through regulating the expression of Interferon-gamma (IFNG). [65], [433]
CIGB-128 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Interferon-gamma (IFNG) is a therapeutic target for CIGB-128. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CIGB-128 through regulating the expression of Interferon-gamma (IFNG). [65], [434]
VPM-4-001 [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Interferon-gamma (IFNG) is a therapeutic target for VPM-4-001. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of VPM-4-001 through regulating the expression of Interferon-gamma (IFNG). [65], [435]
CRx-191 [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Interferon-gamma (IFNG) is a therapeutic target for CRx-191. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CRx-191 through regulating the expression of Interferon-gamma (IFNG). [65], [436]
Fontolizumab [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Interferon-gamma (IFNG) is a therapeutic target for Fontolizumab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Fontolizumab through regulating the expression of Interferon-gamma (IFNG). [65], [437]
TAK-603 [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Interferon-gamma (IFNG) is a therapeutic target for TAK-603. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of TAK-603 through regulating the expression of Interferon-gamma (IFNG). [65], [438]
TG-1042 [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Interferon-gamma (IFNG) is a therapeutic target for TG-1042. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of TG-1042 through regulating the expression of Interferon-gamma (IFNG). [65], [439]
Interleukin-6 (IL6)
Siltuximab [Approved]
In total 2 mechanisms lead to this potential drug response
Response Summary Interleukin-6 (IL6) is a therapeutic target for Siltuximab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Siltuximab through regulating the expression of Interleukin-6 (IL6). [251], [440]
Interleukin-6 (IL6) is a therapeutic target for Siltuximab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Siltuximab through regulating the expression of Interleukin-6 (IL6). [251], [442]
Olokizumab [Phase 3]
In total 2 mechanisms lead to this potential drug response
Response Summary Interleukin-6 (IL6) is a therapeutic target for Olokizumab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Olokizumab through regulating the expression of Interleukin-6 (IL6). [37], [251]
Interleukin-6 (IL6) is a therapeutic target for Olokizumab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Olokizumab through regulating the expression of Interleukin-6 (IL6). [251], [441]
Sirukumab [Phase 3]
In total 2 mechanisms lead to this potential drug response
Response Summary Interleukin-6 (IL6) is a therapeutic target for Sirukumab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Sirukumab through regulating the expression of Interleukin-6 (IL6). [251], [422]
Interleukin-6 (IL6) is a therapeutic target for Sirukumab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Sirukumab through regulating the expression of Interleukin-6 (IL6). [251], [445]
ALD-518 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Interleukin-6 (IL6) is a therapeutic target for ALD-518. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ALD-518 through regulating the expression of Interleukin-6 (IL6). [37], [251]
CDP-6038 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Interleukin-6 (IL6) is a therapeutic target for CDP-6038. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CDP-6038 through regulating the expression of Interleukin-6 (IL6). [90], [251]
Clazakizumab [Phase 2]
In total 2 mechanisms lead to this potential drug response
Response Summary Interleukin-6 (IL6) is a therapeutic target for Clazakizumab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Clazakizumab through regulating the expression of Interleukin-6 (IL6). [37], [251]
Interleukin-6 (IL6) is a therapeutic target for Clazakizumab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Clazakizumab through regulating the expression of Interleukin-6 (IL6). [251], [443]
PF-04236921 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Interleukin-6 (IL6) is a therapeutic target for PF-04236921. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PF-04236921 through regulating the expression of Interleukin-6 (IL6). [251], [444]
YSIL6 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Interleukin-6 (IL6) is a therapeutic target for YSIL6. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of YSIL6 through regulating the expression of Interleukin-6 (IL6). [90], [251]
C326 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Interleukin-6 (IL6) is a therapeutic target for C326. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of C326 through regulating the expression of Interleukin-6 (IL6). [251], [446]
Gerilimzumab [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Interleukin-6 (IL6) is a therapeutic target for Gerilimzumab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Gerilimzumab through regulating the expression of Interleukin-6 (IL6). [251], [447]
MEDI5117 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Interleukin-6 (IL6) is a therapeutic target for MEDI5117. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MEDI5117 through regulating the expression of Interleukin-6 (IL6). [251], [448]
OP-R003 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Interleukin-6 (IL6) is a therapeutic target for OP-R003. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of OP-R003 through regulating the expression of Interleukin-6 (IL6). [37], [251]
Kruppel like factor 4 (KLF4)
APTO-253 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Kruppel like factor 4 (KLF4) is a therapeutic target for APTO-253. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of APTO-253 through regulating the expression of Kruppel like factor 4 (KLF4). [99], [449]
Mammalian target of rapamycin complex 1 (mTORC1)
RBT-101 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Mammalian target of rapamycin complex 1 (mTORC1) is a therapeutic target for RBT-101. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of RBT-101 through regulating the expression of Mammalian target of rapamycin complex 1 (mTORC1). [450], [451]
AZD-2014 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Mammalian target of rapamycin complex 1 (mTORC1) is a therapeutic target for AZD-2014. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AZD-2014 through regulating the expression of Mammalian target of rapamycin complex 1 (mTORC1). [450], [452]
ME-344 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Mammalian target of rapamycin complex 1 (mTORC1) is a therapeutic target for ME-344. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ME-344 through regulating the expression of Mammalian target of rapamycin complex 1 (mTORC1). [15], [450]
NV-5138 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Mammalian target of rapamycin complex 1 (mTORC1) is a therapeutic target for NV-5138. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of NV-5138 through regulating the expression of Mammalian target of rapamycin complex 1 (mTORC1). [450], [453]
Palomid-529 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Mammalian target of rapamycin complex 1 (mTORC1) is a therapeutic target for Palomid-529. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Palomid-529 through regulating the expression of Mammalian target of rapamycin complex 1 (mTORC1). [15], [450]
VS-5584 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Mammalian target of rapamycin complex 1 (mTORC1) is a therapeutic target for VS-5584. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of VS-5584 through regulating the expression of Mammalian target of rapamycin complex 1 (mTORC1). [450], [454]
MAP kinase signal-integrating kinase 2 (MKNK2)
EFT508 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary MAP kinase signal-integrating kinase 2 (MKNK2) is a therapeutic target for EFT508. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of EFT508 through regulating the expression of MAP kinase signal-integrating kinase 2 (MKNK2). [261], [455]
MAPK/ERK kinase kinase 3 (MAP3K3)
ISIS 122970 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary MAPK/ERK kinase kinase 3 (MAP3K3) is a therapeutic target for ISIS 122970. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 122970 through regulating the expression of MAPK/ERK kinase kinase 3 (MAP3K3). [112], [254]
ISIS 122971 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary MAPK/ERK kinase kinase 3 (MAP3K3) is a therapeutic target for ISIS 122971. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 122971 through regulating the expression of MAPK/ERK kinase kinase 3 (MAP3K3). [112], [254]
ISIS 122974 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary MAPK/ERK kinase kinase 3 (MAP3K3) is a therapeutic target for ISIS 122974. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 122974 through regulating the expression of MAPK/ERK kinase kinase 3 (MAP3K3). [112], [254]
ISIS 122975 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary MAPK/ERK kinase kinase 3 (MAP3K3) is a therapeutic target for ISIS 122975. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 122975 through regulating the expression of MAPK/ERK kinase kinase 3 (MAP3K3). [112], [254]
ISIS 122976 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary MAPK/ERK kinase kinase 3 (MAP3K3) is a therapeutic target for ISIS 122976. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 122976 through regulating the expression of MAPK/ERK kinase kinase 3 (MAP3K3). [112], [254]
ISIS 122984 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary MAPK/ERK kinase kinase 3 (MAP3K3) is a therapeutic target for ISIS 122984. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 122984 through regulating the expression of MAPK/ERK kinase kinase 3 (MAP3K3). [112], [254]
ISIS 122985 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary MAPK/ERK kinase kinase 3 (MAP3K3) is a therapeutic target for ISIS 122985. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 122985 through regulating the expression of MAPK/ERK kinase kinase 3 (MAP3K3). [112], [254]
ISIS 122986 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary MAPK/ERK kinase kinase 3 (MAP3K3) is a therapeutic target for ISIS 122986. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 122986 through regulating the expression of MAPK/ERK kinase kinase 3 (MAP3K3). [112], [254]
ISIS 122990 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary MAPK/ERK kinase kinase 3 (MAP3K3) is a therapeutic target for ISIS 122990. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 122990 through regulating the expression of MAPK/ERK kinase kinase 3 (MAP3K3). [112], [254]
ISIS 122991 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary MAPK/ERK kinase kinase 3 (MAP3K3) is a therapeutic target for ISIS 122991. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 122991 through regulating the expression of MAPK/ERK kinase kinase 3 (MAP3K3). [254], [456]
Myb messenger RNA (MYB mRNA)
LR3001 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Myb messenger RNA (MYB mRNA) is a therapeutic target for LR3001. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LR3001 through regulating the expression of Myb messenger RNA (MYB mRNA). [72], [252]
NAD-dependent deacetylase sirtuin-1 (SIRT1)
GSK2245840 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary NAD-dependent deacetylase sirtuin-1 (SIRT1) is a therapeutic target for GSK2245840. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of GSK2245840 through regulating the expression of NAD-dependent deacetylase sirtuin-1 (SIRT1). [457], [458]
MB-12066 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary NAD-dependent deacetylase sirtuin-1 (SIRT1) is a therapeutic target for MB-12066. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MB-12066 through regulating the expression of NAD-dependent deacetylase sirtuin-1 (SIRT1). [457], [459]
SEN-196 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary NAD-dependent deacetylase sirtuin-1 (SIRT1) is a therapeutic target for SEN-196. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SEN-196 through regulating the expression of NAD-dependent deacetylase sirtuin-1 (SIRT1). [457], [460]
SRT2379 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary NAD-dependent deacetylase sirtuin-1 (SIRT1) is a therapeutic target for SRT2379. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SRT2379 through regulating the expression of NAD-dependent deacetylase sirtuin-1 (SIRT1). [457], [461]
SRT3025 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary NAD-dependent deacetylase sirtuin-1 (SIRT1) is a therapeutic target for SRT3025. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SRT3025 through regulating the expression of NAD-dependent deacetylase sirtuin-1 (SIRT1). [457], [462]
(R)-sirtinol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary NAD-dependent deacetylase sirtuin-1 (SIRT1) is a therapeutic target for (R)-sirtinol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of (R)-sirtinol through regulating the expression of NAD-dependent deacetylase sirtuin-1 (SIRT1). [457], [463]
(S)-sirtinol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary NAD-dependent deacetylase sirtuin-1 (SIRT1) is a therapeutic target for (S)-sirtinol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of (S)-sirtinol through regulating the expression of NAD-dependent deacetylase sirtuin-1 (SIRT1). [457], [463]
2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary NAD-dependent deacetylase sirtuin-1 (SIRT1) is a therapeutic target for 2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide through regulating the expression of NAD-dependent deacetylase sirtuin-1 (SIRT1). [457], [464]
2H-chromeno[2,3-d]pyrimidine-2,4(3H)-dione [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary NAD-dependent deacetylase sirtuin-1 (SIRT1) is a therapeutic target for 2H-chromeno[2,3-d]pyrimidine-2,4(3H)-dione. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 2H-chromeno[2,3-d]pyrimidine-2,4(3H)-dione through regulating the expression of NAD-dependent deacetylase sirtuin-1 (SIRT1). [267], [457]
Meta-sirtinol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary NAD-dependent deacetylase sirtuin-1 (SIRT1) is a therapeutic target for Meta-sirtinol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Meta-sirtinol through regulating the expression of NAD-dependent deacetylase sirtuin-1 (SIRT1). [457], [465]
Para-sirtinol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary NAD-dependent deacetylase sirtuin-1 (SIRT1) is a therapeutic target for Para-sirtinol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Para-sirtinol through regulating the expression of NAD-dependent deacetylase sirtuin-1 (SIRT1). [457], [463]
RO-316233 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary NAD-dependent deacetylase sirtuin-1 (SIRT1) is a therapeutic target for RO-316233. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of RO-316233 through regulating the expression of NAD-dependent deacetylase sirtuin-1 (SIRT1). [457], [464]
Ro31-8220 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary NAD-dependent deacetylase sirtuin-1 (SIRT1) is a therapeutic target for Ro31-8220. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ro31-8220 through regulating the expression of NAD-dependent deacetylase sirtuin-1 (SIRT1). [457], [466]
splitomicin [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary NAD-dependent deacetylase sirtuin-1 (SIRT1) is a therapeutic target for splitomicin. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of splitomicin through regulating the expression of NAD-dependent deacetylase sirtuin-1 (SIRT1). [457], [467]
SRT1720 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary NAD-dependent deacetylase sirtuin-1 (SIRT1) is a therapeutic target for SRT1720. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SRT1720 through regulating the expression of NAD-dependent deacetylase sirtuin-1 (SIRT1). [457], [463]
YK-3237 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary NAD-dependent deacetylase sirtuin-1 (SIRT1) is a therapeutic target for YK-3237. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of YK-3237 through regulating the expression of NAD-dependent deacetylase sirtuin-1 (SIRT1). [457], [466]
GSK184072 [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary NAD-dependent deacetylase sirtuin-1 (SIRT1) is a therapeutic target for GSK184072. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of GSK184072 through regulating the expression of NAD-dependent deacetylase sirtuin-1 (SIRT1). [457], [468]
NF-kappa-B inhibitor alpha (NFKBIA)
I3C [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary NF-kappa-B inhibitor alpha (NFKBIA) is a therapeutic target for I3C. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of I3C through regulating the expression of NF-kappa-B inhibitor alpha (NFKBIA). [469], [470]
Fucoxanthin [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary NF-kappa-B inhibitor alpha (NFKBIA) is a therapeutic target for Fucoxanthin. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Fucoxanthin through regulating the expression of NF-kappa-B inhibitor alpha (NFKBIA). [469], [471]
Notch-1 receptor (NOTCH1)
LY3039478 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Notch-1 receptor (NOTCH1) is a therapeutic target for LY3039478. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LY3039478 through regulating the expression of Notch-1 receptor (NOTCH1). [472], [473]
OMP-52M51 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Notch-1 receptor (NOTCH1) is a therapeutic target for OMP-52M51. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of OMP-52M51 through regulating the expression of Notch-1 receptor (NOTCH1). [15], [472]
Peroxisome proliferator-activated receptor alpha (PPARA)
Bezafibrate [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for Bezafibrate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Bezafibrate through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [475]
Ciprofibrate [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for Ciprofibrate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ciprofibrate through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [476]
Fenofibrate [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for Fenofibrate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Fenofibrate through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [477]
Lobeglitazone [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for Lobeglitazone. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Lobeglitazone through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [478]
Pemafibrate [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for Pemafibrate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Pemafibrate through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [475]
BMS-298585 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for BMS-298585. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BMS-298585 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [451], [474]
CS-038 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for CS-038. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CS-038 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [479]
GFT-505 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for GFT-505. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of GFT-505 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [480]
Imiglitazar [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for Imiglitazar. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Imiglitazar through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [481]
Ragaglitazar [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for Ragaglitazar. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ragaglitazar through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [482]
TESAGLITAZAR [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for TESAGLITAZAR. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of TESAGLITAZAR through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [483]
ZYH-1 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for ZYH-1. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ZYH-1 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [484]
GFT14 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for GFT14. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of GFT14 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [485]
LY-518674 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for LY-518674. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LY-518674 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [486]
Naveglitazar [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for Naveglitazar. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Naveglitazar through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [90], [474]
ONO-5129 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for ONO-5129. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ONO-5129 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [487]
ZYH7 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for ZYH7. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ZYH7 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [488]
AVE0897 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for AVE0897. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AVE0897 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [489]
CDT-fenofibrate [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for CDT-fenofibrate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CDT-fenofibrate through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [490]
GW-409544 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for GW-409544. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of GW-409544 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [491]
Oxeglitazar [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for Oxeglitazar. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Oxeglitazar through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [492]
TPST-1120 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for TPST-1120. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of TPST-1120 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [493]
MC-3001 [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for MC-3001. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MC-3001 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [494]
MC-3002 [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for MC-3002. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MC-3002 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [495]
PIRINIXIC ACID [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for PIRINIXIC ACID. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PIRINIXIC ACID through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [496]
Romazarit [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for Romazarit. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Romazarit through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [90], [474]
(9Z,12E)-12-nitrooctadeca-9,12-dienoic acid [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for (9Z,12E)-12-nitrooctadeca-9,12-dienoic acid. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of (9Z,12E)-12-nitrooctadeca-9,12-dienoic acid through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [497]
(E)-12-Nitrooctadec-12-enoic Acid [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for (E)-12-Nitrooctadec-12-enoic Acid. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of (E)-12-Nitrooctadec-12-enoic Acid through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [498]
(E)-13-Nitrooctadec-12-enoic Acid [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for (E)-13-Nitrooctadec-12-enoic Acid. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of (E)-13-Nitrooctadec-12-enoic Acid through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [498]
(E)-4-(3,5-dimethoxystyryl)phenol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for (E)-4-(3,5-dimethoxystyryl)phenol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of (E)-4-(3,5-dimethoxystyryl)phenol through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [499]
8S-HETE [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for 8S-HETE. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 8S-HETE through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [484]
AD-5061 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for AD-5061. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AD-5061 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [500]
BMS-687453 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for BMS-687453. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BMS-687453 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [501]
CP-775146 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for CP-775146. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CP-775146 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [394], [474]
DB-900 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for DB-900. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of DB-900 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [502]
Deoxy-Bigchap [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for Deoxy-Bigchap. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Deoxy-Bigchap through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [503]
DRF 2519 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for DRF 2519. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of DRF 2519 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [504]
eicosatetranoic acid [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for eicosatetranoic acid. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of eicosatetranoic acid through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [505]
Fibrates [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for Fibrates. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Fibrates through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [506]
GSK-9578 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for GSK-9578. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of GSK-9578 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [498]
GW-2331 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for GW-2331. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of GW-2331 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [507]
GW7647 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for GW7647. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of GW7647 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [508]
L-165461 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for L-165461. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of L-165461 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [506]
L-796449 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for L-796449. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of L-796449 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [475]
LL-6531 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for LL-6531. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LL-6531 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [509]
LY-465608 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for LY-465608. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LY-465608 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [510]
N-oleoylethanolamide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for N-oleoylethanolamide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N-oleoylethanolamide through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [511]
pristanic acid [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for pristanic acid. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of pristanic acid through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [512]
reglitazar [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for reglitazar. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of reglitazar through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [513]
TZD18 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for TZD18. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of TZD18 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [514]
ZY H2 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for ZY H2. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ZY H2 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [515]
Aleglitazar [Discontinued in Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for Aleglitazar. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Aleglitazar through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [516]
AR-H049020 [Discontinued in Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for AR-H049020. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AR-H049020 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [512]
AVE-0847 [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for AVE-0847. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AVE-0847 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [517]
AVE-8134 [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for AVE-8134. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AVE-8134 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [518]
BM-17.0744 [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for BM-17.0744. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BM-17.0744 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [90], [474]
BVT-142 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for BVT-142. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BVT-142 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [519]
CS-204 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for CS-204. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CS-204 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [520]
CS-207 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for CS-207. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CS-207 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [521]
DRF 10945 [Discontinued in Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for DRF 10945. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of DRF 10945 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [522]
E-3030 [Discontinued in Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for E-3030. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of E-3030 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [523]
GSK-677954 [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for GSK-677954. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of GSK-677954 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [524]
Indeglitazar [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for Indeglitazar. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Indeglitazar through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [7], [474]
KRP-101 [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for KRP-101. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of KRP-101 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [525]
KRP-105 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for KRP-105. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of KRP-105 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [483]
KRP-297 [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for KRP-297. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of KRP-297 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [512]
LG-101280 [Discontinued in Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for LG-101280. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LG-101280 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [526]
LY-929 [Discontinued in Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for LY-929. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LY-929 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [527]
MP-136 [Discontinued in Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for MP-136. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MP-136 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [528]
NS-220 [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for NS-220. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of NS-220 through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [529]
Reglixane [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for Reglixane. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Reglixane through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [530]
Sipoglitazar [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for Sipoglitazar. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Sipoglitazar through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [531]
Sodelglitazar [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Peroxisome proliferator-activated receptor alpha (PPARA) is a therapeutic target for Sodelglitazar. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Sodelglitazar through regulating the expression of Peroxisome proliferator-activated receptor alpha (PPARA). [474], [532]
PI3-kinase alpha (PIK3CA)
Alpelisib [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase alpha (PIK3CA) is a therapeutic target for Alpelisib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Alpelisib through regulating the expression of PI3-kinase alpha (PIK3CA). [265], [278]
BAY 80-6946 [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase alpha (PIK3CA) is a therapeutic target for BAY 80-6946. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BAY 80-6946 through regulating the expression of PI3-kinase alpha (PIK3CA). [265], [533]
Buparlisib [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase alpha (PIK3CA) is a therapeutic target for Buparlisib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Buparlisib through regulating the expression of PI3-kinase alpha (PIK3CA). [265], [534]
GDC-0032 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase alpha (PIK3CA) is a therapeutic target for GDC-0032. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of GDC-0032 through regulating the expression of PI3-kinase alpha (PIK3CA). [265], [535]
LY3023414 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase alpha (PIK3CA) is a therapeutic target for LY3023414. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LY3023414 through regulating the expression of PI3-kinase alpha (PIK3CA). [265], [536]
MLN1117 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase alpha (PIK3CA) is a therapeutic target for MLN1117. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MLN1117 through regulating the expression of PI3-kinase alpha (PIK3CA). [265], [537]
PA-799 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase alpha (PIK3CA) is a therapeutic target for PA-799. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PA-799 through regulating the expression of PI3-kinase alpha (PIK3CA). [265], [538]
BLY719 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase alpha (PIK3CA) is a therapeutic target for BLY719. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BLY719 through regulating the expression of PI3-kinase alpha (PIK3CA). [90], [265]
HHCYH33 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase alpha (PIK3CA) is a therapeutic target for HHCYH33. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of HHCYH33 through regulating the expression of PI3-kinase alpha (PIK3CA). [265], [539]
PWT-33597 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase alpha (PIK3CA) is a therapeutic target for PWT-33597. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PWT-33597 through regulating the expression of PI3-kinase alpha (PIK3CA). [265], [540]
ETP-46321 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase alpha (PIK3CA) is a therapeutic target for ETP-46321. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ETP-46321 through regulating the expression of PI3-kinase alpha (PIK3CA). [265], [541]
PI3-kinase beta (PIK3CB)
Buparlisib [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for Buparlisib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Buparlisib through regulating the expression of PI3-kinase beta (PIK3CB). [394], [542]
PA-799 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for PA-799. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PA-799 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [543]
PQR309 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for PQR309. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PQR309 through regulating the expression of PI3-kinase beta (PIK3CB). [535], [542]
AZD8186 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for AZD8186. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AZD8186 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [544]
BAY 1082439 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for BAY 1082439. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BAY 1082439 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [545]
GSK2636771 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for GSK2636771. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of GSK2636771 through regulating the expression of PI3-kinase beta (PIK3CB). [90], [542]
3-(4-morpholinothieno[3,2-d]pyrimidin-2-yl)phenol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for 3-(4-morpholinothieno[3,2-d]pyrimidin-2-yl)phenol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 3-(4-morpholinothieno[3,2-d]pyrimidin-2-yl)phenol through regulating the expression of PI3-kinase beta (PIK3CB). [542], [546]
Ethyl 1-[(1H-benzimidazol-2(3H)one-5-yl)sulfonyl]-1H-pyrrole-2-carboxylate [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for Ethyl 1-[(1H-benzimidazol-2(3H)one-5-yl)sulfonyl]-1H-pyrrole-2-carboxylate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ethyl 1-[(1H-benzimidazol-2(3H)one-5-yl)sulfonyl]-1H-pyrrole-2-carboxylate through regulating the expression of PI3-kinase beta (PIK3CB). [542], [547]
ISIS 31963 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for ISIS 31963. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 31963 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [548]
ISIS 31982 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for ISIS 31982. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 31982 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [548]
ISIS 31996 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for ISIS 31996. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 31996 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [548]
ISIS 32000 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for ISIS 32000. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 32000 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [548]
ISIS 32002 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for ISIS 32002. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 32002 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [548]
ISIS 32003 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for ISIS 32003. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 32003 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [548]
ISIS 32004 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for ISIS 32004. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 32004 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [548]
ISIS 32005 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for ISIS 32005. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 32005 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [548]
ISIS 32006 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for ISIS 32006. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 32006 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [548]
ISIS 32008 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for ISIS 32008. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 32008 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [548]
ISIS 32010 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for ISIS 32010. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 32010 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [548]
ISIS 32014 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for ISIS 32014. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 32014 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [548]
ISIS 32015 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for ISIS 32015. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 32015 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [548]
ISIS 32020 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for ISIS 32020. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 32020 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [548]
ISIS 32021 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for ISIS 32021. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 32021 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [548]
ISIS 32024 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for ISIS 32024. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 32024 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [548]
ISIS 32028 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for ISIS 32028. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 32028 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [548]
ISIS 32035 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for ISIS 32035. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 32035 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [548]
ISIS 32039 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for ISIS 32039. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 32039 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [549]
KU-0060648 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for KU-0060648. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of KU-0060648 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [550]
LY-292223 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for LY-292223. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LY-292223 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [549]
PI-3065 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for PI-3065. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PI-3065 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [547]
PIK-75 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for PIK-75. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PIK-75 through regulating the expression of PI3-kinase beta (PIK3CB). [349], [542]
PP121 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for PP121. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PP121 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [551]
TGX-221 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary PI3-kinase beta (PIK3CB) is a therapeutic target for TGX-221. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of TGX-221 through regulating the expression of PI3-kinase beta (PIK3CB). [542], [552]
Protein arginine methyltransferase 1 (PRMT1)
GSK3368715 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Protein arginine methyltransferase 1 (PRMT1) is a therapeutic target for GSK3368715. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of GSK3368715 through regulating the expression of Protein arginine methyltransferase 1 (PRMT1). [553], [554]
AMI-1 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Protein arginine methyltransferase 1 (PRMT1) is a therapeutic target for AMI-1. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AMI-1 through regulating the expression of Protein arginine methyltransferase 1 (PRMT1). [553], [555]
RM65 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Protein arginine methyltransferase 1 (PRMT1) is a therapeutic target for RM65. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of RM65 through regulating the expression of Protein arginine methyltransferase 1 (PRMT1). [553], [556]
Protein phosphatase 1A (PPM1A)
VP-102 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Protein phosphatase 1A (PPM1A) is a therapeutic target for VP-102. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of VP-102 through regulating the expression of Protein phosphatase 1A (PPM1A). [75], [557]
Proto-oncogene c-Myc (MYC)
AVI-5126 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Proto-oncogene c-Myc (MYC) is a therapeutic target for AVI-5126. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AVI-5126 through regulating the expression of Proto-oncogene c-Myc (MYC). [368], [558]
Resten-NG [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Proto-oncogene c-Myc (MYC) is a therapeutic target for Resten-NG. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Resten-NG through regulating the expression of Proto-oncogene c-Myc (MYC). [368], [559]
TWS-119 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Proto-oncogene c-Myc (MYC) is a therapeutic target for TWS-119. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of TWS-119 through regulating the expression of Proto-oncogene c-Myc (MYC). [42], [368]
RAC-alpha serine/threonine-protein kinase (AKT1)
AZD5363 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for AZD5363. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AZD5363 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [15], [265]
Enzastaurin [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for Enzastaurin. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Enzastaurin through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [560]
GDC-0068 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for GDC-0068. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of GDC-0068 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [15], [265]
ARQ 092 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for ARQ 092. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ARQ 092 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [561]
CI-1033 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for CI-1033. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CI-1033 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [15], [265]
CMX-2043 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for CMX-2043. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CMX-2043 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [266]
GSK2110183 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for GSK2110183. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of GSK2110183 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [562]
PTX-200 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for PTX-200. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PTX-200 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [15], [265]
RX-0201 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for RX-0201. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of RX-0201 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [563]
Triciribine prodrug [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for Triciribine prodrug. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Triciribine prodrug through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [315]
ARQ 751 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for ARQ 751. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ARQ 751 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [563]
BMS-754807 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for BMS-754807. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BMS-754807 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [564]
M2698 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for M2698. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of M2698 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [15], [265]
(Z)-3-((1H-pyrrol-2-yl)methylene)indolin-2-one [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for (Z)-3-((1H-pyrrol-2-yl)methylene)indolin-2-one. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of (Z)-3-((1H-pyrrol-2-yl)methylene)indolin-2-one through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [369]
4,5,6,7-tetrabromo-1H-benzo[d][1,2,3]triazole [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for 4,5,6,7-tetrabromo-1H-benzo[d][1,2,3]triazole. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 4,5,6,7-tetrabromo-1H-benzo[d][1,2,3]triazole through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [408]
4,5,6-trihydroxy-3-methylphthalide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for 4,5,6-trihydroxy-3-methylphthalide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 4,5,6-trihydroxy-3-methylphthalide through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [369]
A-443654 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for A-443654. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of A-443654 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [369]
A-674563 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for A-674563. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of A-674563 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [565]
Akt inhibitor VIII [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for Akt inhibitor VIII. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Akt inhibitor VIII through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [394]
ALM-301 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for ALM-301. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ALM-301 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [566]
Bisindolylmaleimide-I [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for Bisindolylmaleimide-I. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Bisindolylmaleimide-I through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [567]
BMS 536924 [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for BMS 536924. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BMS 536924 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [369]
BX-517 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for BX-517. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BX-517 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [386]
CI-1040 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for CI-1040. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CI-1040 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [563]
Inositol 1,3,4,5-Tetrakisphosphate [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for Inositol 1,3,4,5-Tetrakisphosphate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Inositol 1,3,4,5-Tetrakisphosphate through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [568]
KN-62 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for KN-62. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of KN-62 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [567]
Lactoquinomycin [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for Lactoquinomycin. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Lactoquinomycin through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [569]
LD-101 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for LD-101. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LD-101 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [563]
MYRIOCIN [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for MYRIOCIN. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MYRIOCIN through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [570]
NU-1001-41 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for NU-1001-41. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of NU-1001-41 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [563]
RO-316233 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for RO-316233. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of RO-316233 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [369]
Ro31-8220 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for Ro31-8220. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ro31-8220 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [571]
SB-747651A [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for SB-747651A. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SB-747651A through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [376]
STAUROSPORINONE [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for STAUROSPORINONE. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of STAUROSPORINONE through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [570]
VLI-27 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for VLI-27. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of VLI-27 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [265], [563]
Squalestatin 1 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary RAC-alpha serine/threonine-protein kinase (AKT1) is a therapeutic target for Squalestatin 1. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Squalestatin 1 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [15], [265]
Retinoic acid-inducible gene-1 (RIG-1)
SB-9200 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Retinoic acid-inducible gene-1 (RIG-1) is a therapeutic target for SB-9200. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SB-9200 through regulating the expression of Retinoic acid-inducible gene-1 (RIG-1). [572], [573]
CV8102 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Retinoic acid-inducible gene-1 (RIG-1) is a therapeutic target for CV8102. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CV8102 through regulating the expression of Retinoic acid-inducible gene-1 (RIG-1). [572], [574]
MK-4621 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Retinoic acid-inducible gene-1 (RIG-1) is a therapeutic target for MK-4621. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MK-4621 through regulating the expression of Retinoic acid-inducible gene-1 (RIG-1). [572], [575]
Serine/threonine-protein kinase mTOR (mTOR)
Glasdegib [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for Glasdegib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Glasdegib through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [577]
Novolimus [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for Novolimus. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Novolimus through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [379], [576]
Temsirolimus [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for Temsirolimus. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Temsirolimus through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [578]
Zotarolimus [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for Zotarolimus. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Zotarolimus through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [263], [576]
Ridaforolimus [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for Ridaforolimus. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ridaforolimus through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [579]
ABI-009 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for ABI-009. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ABI-009 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [580]
AZD-2014 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for AZD-2014. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AZD-2014 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [263], [576]
BEZ235 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for BEZ235. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BEZ235 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [15], [576]
BGT226 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for BGT226. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BGT226 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [263], [576]
CC-223 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for CC-223. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CC-223 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [581]
INK128 [Phase 2]
In total 2 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for INK128. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of INK128 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [582]
Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for INK128. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of INK128 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [599]
LY3023414 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for LY3023414. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LY3023414 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [583]
ME-344 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for ME-344. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ME-344 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [584]
MM-141 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for MM-141. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MM-141 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [15], [576]
OSI-027 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for OSI-027. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of OSI-027 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [585]
PF-04691502 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for PF-04691502. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PF-04691502 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [586]
PF-05212384 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for PF-05212384. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PF-05212384 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [537], [576]
PQR309 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for PQR309. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PQR309 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [535], [576]
Salirasib [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for Salirasib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Salirasib through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [263], [576]
SAR245409 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for SAR245409. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SAR245409 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [587]
SF1126 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for SF1126. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SF1126 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [15], [576]
BI 860585 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for BI 860585. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BI 860585 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [588]
DS-3078 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for DS-3078. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of DS-3078 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [589]
DS-7423 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for DS-7423. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of DS-7423 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [590]
GDC-0349 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for GDC-0349. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of GDC-0349 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [263], [576]
LAM-001 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for LAM-001. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LAM-001 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [591]
PWT-33597 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for PWT-33597. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PWT-33597 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [315], [576]
VS-5584 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for VS-5584. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of VS-5584 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [592]
(4-(6-morpholino-9H-purin-2-yl)phenyl)methanol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for (4-(6-morpholino-9H-purin-2-yl)phenyl)methanol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of (4-(6-morpholino-9H-purin-2-yl)phenyl)methanol through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [593]
2-(2-Methyl-morpholin-4-yl)-benzo[h]chromen-4-one [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for 2-(2-Methyl-morpholin-4-yl)-benzo[h]chromen-4-one. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 2-(2-Methyl-morpholin-4-yl)-benzo[h]chromen-4-one through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [594]
2-(6-morpholino-9H-purin-2-yl)phenol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for 2-(6-morpholino-9H-purin-2-yl)phenol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 2-(6-morpholino-9H-purin-2-yl)phenol through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [593]
2-chloro-N-(6-cyanopyridin-3-yl)propanamide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for 2-chloro-N-(6-cyanopyridin-3-yl)propanamide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 2-chloro-N-(6-cyanopyridin-3-yl)propanamide through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [595]
2-Morpholin-4-yl-pyrimido[2,1-a]isoquinolin-4-one [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for 2-Morpholin-4-yl-pyrimido[2,1-a]isoquinolin-4-one. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 2-Morpholin-4-yl-pyrimido[2,1-a]isoquinolin-4-one through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [596]
3-(6-morpholino-9H-purin-2-yl)phenol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for 3-(6-morpholino-9H-purin-2-yl)phenol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 3-(6-morpholino-9H-purin-2-yl)phenol through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [593]
4-(2-(1H-indol-6-yl)-9H-purin-6-yl)morpholine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for 4-(2-(1H-indol-6-yl)-9H-purin-6-yl)morpholine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 4-(2-(1H-indol-6-yl)-9H-purin-6-yl)morpholine through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [593]
4-(2-(thiophen-2-yl)-9H-purin-6-yl)morpholine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for 4-(2-(thiophen-2-yl)-9H-purin-6-yl)morpholine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 4-(2-(thiophen-2-yl)-9H-purin-6-yl)morpholine through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [597]
4-(2-(thiophen-3-yl)-9H-purin-6-yl)morpholine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for 4-(2-(thiophen-3-yl)-9H-purin-6-yl)morpholine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 4-(2-(thiophen-3-yl)-9H-purin-6-yl)morpholine through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [593]
4-(6-morpholino-9H-purin-2-yl)phenol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for 4-(6-morpholino-9H-purin-2-yl)phenol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 4-(6-morpholino-9H-purin-2-yl)phenol through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [593]
AP-21967 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for AP-21967. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AP-21967 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [594]
AR-mTOR-26 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for AR-mTOR-26. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AR-mTOR-26 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [263], [576]
C-16-(S)-3-methylindolerapamycin [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for C-16-(S)-3-methylindolerapamycin. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of C-16-(S)-3-methylindolerapamycin through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [593]
CU-906 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for CU-906. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CU-906 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [263], [576]
EC-0565 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for EC-0565. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of EC-0565 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [263], [576]
EC-0845 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for EC-0845. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of EC-0845 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [263], [576]
EM-101 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for EM-101. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of EM-101 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [598]
Ethyl 1-[(1H-benzimidazol-2(3H)one-5-yl)sulfonyl]-1H-pyrrole-2-carboxylate [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for Ethyl 1-[(1H-benzimidazol-2(3H)one-5-yl)sulfonyl]-1H-pyrrole-2-carboxylate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ethyl 1-[(1H-benzimidazol-2(3H)one-5-yl)sulfonyl]-1H-pyrrole-2-carboxylate through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [596]
HM-5016699 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for HM-5016699. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of HM-5016699 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [263], [576]
OXA-01 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for OXA-01. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of OXA-01 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [263], [576]
P-2281 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for P-2281. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of P-2281 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [263], [576]
P-6915 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for P-6915. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of P-6915 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [263], [576]
PF-03772304 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for PF-03772304. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PF-03772304 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [263], [576]
PF-05094037 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for PF-05094037. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PF-05094037 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [600]
PP-242 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for PP-242. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PP-242 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [340], [576]
PP121 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for PP121. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PP121 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [349], [576]
Rapamycin complexed with immunophilin FKBP12 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for Rapamycin complexed with immunophilin FKBP12. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Rapamycin complexed with immunophilin FKBP12 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [596]
SB-2280 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for SB-2280. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SB-2280 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [263], [576]
SX-MTR1 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for SX-MTR1. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SX-MTR1 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [263], [576]
torin 1 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for torin 1. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of torin 1 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [349], [576]
Torin2 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for Torin2. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Torin2 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [601]
X-387 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for X-387. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of X-387 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [263], [576]
AZD8055 [Discontinued in Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for AZD8055. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AZD8055 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [602]
SCR-44001 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for SCR-44001. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SCR-44001 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [603]
TAFA-93 [Discontinued in Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Serine/threonine-protein kinase mTOR (mTOR) is a therapeutic target for TAFA-93. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of TAFA-93 through regulating the expression of Serine/threonine-protein kinase mTOR (mTOR). [576], [604]
Signal transducer and activator of transcription 1 (STAT1)
AVT-02 UE [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 1 (STAT1) is a therapeutic target for AVT-02 UE. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AVT-02 UE through regulating the expression of Signal transducer and activator of transcription 1 (STAT1). [65], [605]
Solute carrier family 40 member 1 (SLC40A1)
LY2928057 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Solute carrier family 40 member 1 (SLC40A1) is a therapeutic target for LY2928057. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of LY2928057 through regulating the expression of Solute carrier family 40 member 1 (SLC40A1). [34], [606]
Ferroportin mab [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Solute carrier family 40 member 1 (SLC40A1) is a therapeutic target for Ferroportin mab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ferroportin mab through regulating the expression of Solute carrier family 40 member 1 (SLC40A1). [34], [607]
M012 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Solute carrier family 40 member 1 (SLC40A1) is a therapeutic target for M012. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of M012 through regulating the expression of Solute carrier family 40 member 1 (SLC40A1). [34], [608]
SRSF protein kinase 1 (SRPK1)
SPHINX31 [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary SRSF protein kinase 1 (SRPK1) is a therapeutic target for SPHINX31. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of SPHINX31 through regulating the expression of SRSF protein kinase 1 (SRPK1). [254], [609]
Target of rapamycin complex 2 MAPKAP1 (MTORC2)
AZD-2014 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Target of rapamycin complex 2 MAPKAP1 (MTORC2) is a therapeutic target for AZD-2014. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AZD-2014 through regulating the expression of Target of rapamycin complex 2 MAPKAP1 (MTORC2). [394], [610]
ME-344 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Target of rapamycin complex 2 MAPKAP1 (MTORC2) is a therapeutic target for ME-344. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ME-344 through regulating the expression of Target of rapamycin complex 2 MAPKAP1 (MTORC2). [15], [610]
Palomid-529 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Target of rapamycin complex 2 MAPKAP1 (MTORC2) is a therapeutic target for Palomid-529. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Palomid-529 through regulating the expression of Target of rapamycin complex 2 MAPKAP1 (MTORC2). [15], [610]
VS-5584 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Target of rapamycin complex 2 MAPKAP1 (MTORC2) is a therapeutic target for VS-5584. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of VS-5584 through regulating the expression of Target of rapamycin complex 2 MAPKAP1 (MTORC2). [453], [610]
Thrombospondin-1 (THBS1)
ABT-510 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Thrombospondin-1 (THBS1) is a therapeutic target for ABT-510. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ABT-510 through regulating the expression of Thrombospondin-1 (THBS1). [611], [612]
CVX-045 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Thrombospondin-1 (THBS1) is a therapeutic target for CVX-045. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CVX-045 through regulating the expression of Thrombospondin-1 (THBS1). [611], [613]
Thymidine kinase 1 (TK1)
DEOXYCYTIDINE [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for DEOXYCYTIDINE. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of DEOXYCYTIDINE through regulating the expression of Thymidine kinase 1 (TK1). [368], [394]
Penciclovir [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for Penciclovir. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Penciclovir through regulating the expression of Thymidine kinase 1 (TK1). [368], [614]
TK-DLI [Preregistration]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for TK-DLI. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of TK-DLI through regulating the expression of Thymidine kinase 1 (TK1). [368], [394]
FV-100 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for FV-100. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of FV-100 through regulating the expression of Thymidine kinase 1 (TK1). [368], [615]
Radiosensitizer gene therapy [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for Radiosensitizer gene therapy. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Radiosensitizer gene therapy through regulating the expression of Thymidine kinase 1 (TK1). [368], [616]
RP101 [Phase 2/3]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for RP101. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of RP101 through regulating the expression of Thymidine kinase 1 (TK1). [368], [394]
HQK-1004 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for HQK-1004. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of HQK-1004 through regulating the expression of Thymidine kinase 1 (TK1). [368], [617]
Rilapladib [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for Rilapladib. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Rilapladib through regulating the expression of Thymidine kinase 1 (TK1). [368], [618]
Thymidine kinase-expressing adenovirus and ganciclovir suicide gene therapy [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for Thymidine kinase-expressing adenovirus and ganciclovir suicide gene therapy. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Thymidine kinase-expressing adenovirus and ganciclovir suicide gene therapy through regulating the expression of Thymidine kinase 1 (TK1). [368], [619]
(South)-Methanocarba-Thymidine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for (South)-Methanocarba-Thymidine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of (South)-Methanocarba-Thymidine through regulating the expression of Thymidine kinase 1 (TK1). [368], [394]
1-[(Z)-4-(triphenylmethoxy)-2-butenyl]thymine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for 1-[(Z)-4-(triphenylmethoxy)-2-butenyl]thymine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 1-[(Z)-4-(triphenylmethoxy)-2-butenyl]thymine through regulating the expression of Thymidine kinase 1 (TK1). [368], [620]
1-[2-(2-triphenylmethoxyethoxy)ethyl]thymine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for 1-[2-(2-triphenylmethoxyethoxy)ethyl]thymine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 1-[2-(2-triphenylmethoxyethoxy)ethyl]thymine through regulating the expression of Thymidine kinase 1 (TK1). [368], [620]
1-[5-(triphenylmethoxy)pentyl]thymine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for 1-[5-(triphenylmethoxy)pentyl]thymine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 1-[5-(triphenylmethoxy)pentyl]thymine through regulating the expression of Thymidine kinase 1 (TK1). [368], [620]
1-[6-(triphenylmethoxy)hexyl]thymine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for 1-[6-(triphenylmethoxy)hexyl]thymine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 1-[6-(triphenylmethoxy)hexyl]thymine through regulating the expression of Thymidine kinase 1 (TK1). [368], [620]
1-[7-(triphenylmethoxy)heptyl]thymine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for 1-[7-(triphenylmethoxy)heptyl]thymine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 1-[7-(triphenylmethoxy)heptyl]thymine through regulating the expression of Thymidine kinase 1 (TK1). [368], [621]
2'-deoxythymidine triphosphate [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for 2'-deoxythymidine triphosphate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 2'-deoxythymidine triphosphate through regulating the expression of Thymidine kinase 1 (TK1). [368], [618]
2'-Deoxyuridine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for 2'-Deoxyuridine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 2'-Deoxyuridine through regulating the expression of Thymidine kinase 1 (TK1). [368], [622]
3'-(1,2,3-Triazol-1-yl)-3'-deoxy-beta-D-thymidine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for 3'-(1,2,3-Triazol-1-yl)-3'-deoxy-beta-D-thymidine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 3'-(1,2,3-Triazol-1-yl)-3'-deoxy-beta-D-thymidine through regulating the expression of Thymidine kinase 1 (TK1). [368], [614]
3-(2-propyn-1-yl)thymidine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for 3-(2-propyn-1-yl)thymidine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 3-(2-propyn-1-yl)thymidine through regulating the expression of Thymidine kinase 1 (TK1). [368], [623]
5-Bromothienyldeoxyuridine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for 5-Bromothienyldeoxyuridine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 5-Bromothienyldeoxyuridine through regulating the expression of Thymidine kinase 1 (TK1). [368], [394]
5-Iodo-2'-Deoxyuridine-5'-Monophosphate [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for 5-Iodo-2'-Deoxyuridine-5'-Monophosphate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 5-Iodo-2'-Deoxyuridine-5'-Monophosphate through regulating the expression of Thymidine kinase 1 (TK1). [368], [394]
5-propyl-2'-deoxyuridine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for 5-propyl-2'-deoxyuridine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 5-propyl-2'-deoxyuridine through regulating the expression of Thymidine kinase 1 (TK1). [368], [623]
6-(Dihydroxy-Isobutyl)-Thymine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for 6-(Dihydroxy-Isobutyl)-Thymine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 6-(Dihydroxy-Isobutyl)-Thymine through regulating the expression of Thymidine kinase 1 (TK1). [368], [394]
6-Hydroxypropylthymine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for 6-Hydroxypropylthymine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 6-Hydroxypropylthymine through regulating the expression of Thymidine kinase 1 (TK1). [368], [624]
9-(4-Hydroxybutyl)-N2-Phenylguanine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for 9-(4-Hydroxybutyl)-N2-Phenylguanine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 9-(4-Hydroxybutyl)-N2-Phenylguanine through regulating the expression of Thymidine kinase 1 (TK1). [368], [394]
9-Hydroxypropyladenine, R-Isomer [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for 9-Hydroxypropyladenine, R-Isomer. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 9-Hydroxypropyladenine, R-Isomer through regulating the expression of Thymidine kinase 1 (TK1). [368], [394]
9-Hydroxypropyladenine, S-Isomer [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for 9-Hydroxypropyladenine, S-Isomer. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 9-Hydroxypropyladenine, S-Isomer through regulating the expression of Thymidine kinase 1 (TK1). [368], [394]
BVDU-MP [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for BVDU-MP. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BVDU-MP through regulating the expression of Thymidine kinase 1 (TK1). [368], [625]
Deoxythymidine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for Deoxythymidine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Deoxythymidine through regulating the expression of Thymidine kinase 1 (TK1). [368], [394]
Edoxudine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for Edoxudine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Edoxudine through regulating the expression of Thymidine kinase 1 (TK1). [368], [623]
ITdU [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for ITdU. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ITdU through regulating the expression of Thymidine kinase 1 (TK1). [368], [620]
L-5-(bromovinyl)deoxyuridine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for L-5-(bromovinyl)deoxyuridine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of L-5-(bromovinyl)deoxyuridine through regulating the expression of Thymidine kinase 1 (TK1). [368], [626]
L-5-iodo-2'-deoxyuridine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for L-5-iodo-2'-deoxyuridine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of L-5-iodo-2'-deoxyuridine through regulating the expression of Thymidine kinase 1 (TK1). [368], [623]
N2-(3-trifluoromethylphenyl)guanine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for N2-(3-trifluoromethylphenyl)guanine. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of N2-(3-trifluoromethylphenyl)guanine through regulating the expression of Thymidine kinase 1 (TK1). [368], [623]
P1-(5'-Adenosyl)P5-(5'-Thymidyl)Pentaphosphate [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for P1-(5'-Adenosyl)P5-(5'-Thymidyl)Pentaphosphate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of P1-(5'-Adenosyl)P5-(5'-Thymidyl)Pentaphosphate through regulating the expression of Thymidine kinase 1 (TK1). [368], [394]
Thymidine-5'-Phosphate [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for Thymidine-5'-Phosphate. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Thymidine-5'-Phosphate through regulating the expression of Thymidine kinase 1 (TK1). [368], [394]
Sitimagene ceradenovec [Discontinued in Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Thymidine kinase 1 (TK1) is a therapeutic target for Sitimagene ceradenovec. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Sitimagene ceradenovec through regulating the expression of Thymidine kinase 1 (TK1). [368], [627]
Tumor necrosis factor (TNF)
Adalimumab [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Adalimumab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Adalimumab through regulating the expression of Tumor necrosis factor (TNF). [628], [629]
Certolizumab [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Certolizumab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Certolizumab through regulating the expression of Tumor necrosis factor (TNF). [628], [630]
Enbrel [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Enbrel. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Enbrel through regulating the expression of Tumor necrosis factor (TNF). [628], [631]
Etanercept [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Etanercept. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Etanercept through regulating the expression of Tumor necrosis factor (TNF). [628], [632]
Golimumab [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Golimumab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Golimumab through regulating the expression of Tumor necrosis factor (TNF). [628], [633]
Infliximab [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Infliximab. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Infliximab through regulating the expression of Tumor necrosis factor (TNF). [628], [634]
Lenalidomide [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Lenalidomide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Lenalidomide through regulating the expression of Tumor necrosis factor (TNF). [628], [635]
Nafamostat [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Nafamostat. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Nafamostat through regulating the expression of Tumor necrosis factor (TNF). [628], [636]
Pentoxifylline [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Pentoxifylline. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Pentoxifylline through regulating the expression of Tumor necrosis factor (TNF). [628], [637]
Thalidomide [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Thalidomide. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Thalidomide through regulating the expression of Tumor necrosis factor (TNF). [604], [628]
ABP 501 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for ABP 501. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ABP 501 through regulating the expression of Tumor necrosis factor (TNF). [628], [638]
CPL-7075 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for CPL-7075. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CPL-7075 through regulating the expression of Tumor necrosis factor (TNF). [628], [639]
Golnerminogene pradenovac [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Golnerminogene pradenovac. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Golnerminogene pradenovac through regulating the expression of Tumor necrosis factor (TNF). [628], [640]
PF-06410293 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for PF-06410293. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PF-06410293 through regulating the expression of Tumor necrosis factor (TNF). [628], [641]
PF-06438179 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for PF-06438179. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PF-06438179 through regulating the expression of Tumor necrosis factor (TNF). [628], [642]
ABT-122 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for ABT-122. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ABT-122 through regulating the expression of Tumor necrosis factor (TNF). [628], [643]
AN0128 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for AN0128. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AN0128 through regulating the expression of Tumor necrosis factor (TNF). [628], [644]
AP-301-IH [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for AP-301-IH. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AP-301-IH through regulating the expression of Tumor necrosis factor (TNF). [628], [645]
ART621 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for ART621. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ART621 through regulating the expression of Tumor necrosis factor (TNF). [313], [628]
BAICALEIN [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for BAICALEIN. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BAICALEIN through regulating the expression of Tumor necrosis factor (TNF). [628], [646]
COVA322 [Phase 1/2a]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for COVA322. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of COVA322 through regulating the expression of Tumor necrosis factor (TNF). [628], [647]
DLX-105 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for DLX-105. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of DLX-105 through regulating the expression of Tumor necrosis factor (TNF). [628], [648]
ESBA-105 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for ESBA-105. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ESBA-105 through regulating the expression of Tumor necrosis factor (TNF). [628], [649]
Ortataxel [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Ortataxel. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Ortataxel through regulating the expression of Tumor necrosis factor (TNF). [628], [650]
Pegsunercept [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Pegsunercept. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Pegsunercept through regulating the expression of Tumor necrosis factor (TNF). [628], [651]
RDP58 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for RDP58. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of RDP58 through regulating the expression of Tumor necrosis factor (TNF). [628], [652]
TNF alpha kinoid [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for TNF alpha kinoid. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of TNF alpha kinoid through regulating the expression of Tumor necrosis factor (TNF). [628], [653]
ABBV-257 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for ABBV-257. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ABBV-257 through regulating the expression of Tumor necrosis factor (TNF). [628], [654]
AST-005 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for AST-005. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AST-005 through regulating the expression of Tumor necrosis factor (TNF). [37], [628]
AVX-470 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for AVX-470. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AVX-470 through regulating the expression of Tumor necrosis factor (TNF). [37], [628]
CYT-609 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for CYT-609. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CYT-609 through regulating the expression of Tumor necrosis factor (TNF). [628], [655]
INB03 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for INB03. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of INB03 through regulating the expression of Tumor necrosis factor (TNF). [628], [656]
PF-05230905 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for PF-05230905. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PF-05230905 through regulating the expression of Tumor necrosis factor (TNF). [39], [628]
PMI-005 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for PMI-005. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PMI-005 through regulating the expression of Tumor necrosis factor (TNF). [628], [657]
ABX-0401 [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for ABX-0401. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ABX-0401 through regulating the expression of Tumor necrosis factor (TNF). [6], [628]
Celastrol [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Celastrol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Celastrol through regulating the expression of Tumor necrosis factor (TNF). [90], [628]
2-Propanol, Isopropanol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for 2-Propanol, Isopropanol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of 2-Propanol, Isopropanol through regulating the expression of Tumor necrosis factor (TNF). [628], [658]
DOM-0215 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for DOM-0215. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of DOM-0215 through regulating the expression of Tumor necrosis factor (TNF). [628], [659]
IK-862 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for IK-862. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of IK-862 through regulating the expression of Tumor necrosis factor (TNF). [628], [660]
PKF-241-466 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for PKF-241-466. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PKF-241-466 through regulating the expression of Tumor necrosis factor (TNF). [628], [660]
PKF-242-484 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for PKF-242-484. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PKF-242-484 through regulating the expression of Tumor necrosis factor (TNF). [507], [628]
Y-39041 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Y-39041. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Y-39041 through regulating the expression of Tumor necrosis factor (TNF). [628], [661]
ALS-00T2-0501 [Discontinued in Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for ALS-00T2-0501. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ALS-00T2-0501 through regulating the expression of Tumor necrosis factor (TNF). [628], [662]
AME-527 [Discontinued in Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for AME-527. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AME-527 through regulating the expression of Tumor necrosis factor (TNF). [628], [659]
Camobucol [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Camobucol. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Camobucol through regulating the expression of Tumor necrosis factor (TNF). [628], [663]
CDP571 [Discontinued in Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for CDP571. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CDP571 through regulating the expression of Tumor necrosis factor (TNF). [628], [664]
CRx-191 [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for CRx-191. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CRx-191 through regulating the expression of Tumor necrosis factor (TNF). [628], [665]
CYT-007-TNFQb [Discontinued in Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for CYT-007-TNFQb. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of CYT-007-TNFQb through regulating the expression of Tumor necrosis factor (TNF). [435], [628]
FR-133605 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for FR-133605. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of FR-133605 through regulating the expression of Tumor necrosis factor (TNF). [628], [666]
ISIS 104838 [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for ISIS 104838. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 104838 through regulating the expression of Tumor necrosis factor (TNF). [628], [667]
MDL-201112 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for MDL-201112. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MDL-201112 through regulating the expression of Tumor necrosis factor (TNF). [628], [668]
PNU-282987 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for PNU-282987. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PNU-282987 through regulating the expression of Tumor necrosis factor (TNF). [26], [628]
Segard [Discontinued in Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Segard. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Segard through regulating the expression of Tumor necrosis factor (TNF). [628], [669]
TNFQb therapeutic vaccines [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for TNFQb therapeutic vaccines. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of TNFQb therapeutic vaccines through regulating the expression of Tumor necrosis factor (TNF). [628], [670]
Tyrosine-protein kinase EIF2AK2 (p68)
ASN-11124542 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Tyrosine-protein kinase EIF2AK2 (p68) is a therapeutic target for ASN-11124542. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ASN-11124542 through regulating the expression of Tyrosine-protein kinase EIF2AK2 (p68). [671], [672]
NU6140 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Tyrosine-protein kinase EIF2AK2 (p68) is a therapeutic target for NU6140. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of NU6140 through regulating the expression of Tyrosine-protein kinase EIF2AK2 (p68). [671], [673]
Ubiquitin-protein ligase E3 Mdm2 (MDM2)
RG7388 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Ubiquitin-protein ligase E3 Mdm2 (MDM2) is a therapeutic target for RG7388. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of RG7388 through regulating the expression of Ubiquitin-protein ligase E3 Mdm2 (MDM2). [89], [674]
ALRN-6924 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Ubiquitin-protein ligase E3 Mdm2 (MDM2) is a therapeutic target for ALRN-6924. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ALRN-6924 through regulating the expression of Ubiquitin-protein ligase E3 Mdm2 (MDM2). [89], [675]
AMG 232 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Ubiquitin-protein ligase E3 Mdm2 (MDM2) is a therapeutic target for AMG 232. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of AMG 232 through regulating the expression of Ubiquitin-protein ligase E3 Mdm2 (MDM2). [15], [89]
APG-115 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Ubiquitin-protein ligase E3 Mdm2 (MDM2) is a therapeutic target for APG-115. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of APG-115 through regulating the expression of Ubiquitin-protein ligase E3 Mdm2 (MDM2). [89], [676]
ASTX295 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Ubiquitin-protein ligase E3 Mdm2 (MDM2) is a therapeutic target for ASTX295. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ASTX295 through regulating the expression of Ubiquitin-protein ligase E3 Mdm2 (MDM2). [89], [677]
BI 907828 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Ubiquitin-protein ligase E3 Mdm2 (MDM2) is a therapeutic target for BI 907828. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of BI 907828 through regulating the expression of Ubiquitin-protein ligase E3 Mdm2 (MDM2). [89], [678]
DS-3032 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Ubiquitin-protein ligase E3 Mdm2 (MDM2) is a therapeutic target for DS-3032. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of DS-3032 through regulating the expression of Ubiquitin-protein ligase E3 Mdm2 (MDM2). [89], [679]
HDM201 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Ubiquitin-protein ligase E3 Mdm2 (MDM2) is a therapeutic target for HDM201. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of HDM201 through regulating the expression of Ubiquitin-protein ligase E3 Mdm2 (MDM2). [89], [680]
JNJ-26854165 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Ubiquitin-protein ligase E3 Mdm2 (MDM2) is a therapeutic target for JNJ-26854165. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of JNJ-26854165 through regulating the expression of Ubiquitin-protein ligase E3 Mdm2 (MDM2). [15], [89]
RG7775 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Ubiquitin-protein ligase E3 Mdm2 (MDM2) is a therapeutic target for RG7775. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of RG7775 through regulating the expression of Ubiquitin-protein ligase E3 Mdm2 (MDM2). [89], [681]
ISIS 16507 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Ubiquitin-protein ligase E3 Mdm2 (MDM2) is a therapeutic target for ISIS 16507. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 16507 through regulating the expression of Ubiquitin-protein ligase E3 Mdm2 (MDM2). [74], [89]
ISIS 16518 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Ubiquitin-protein ligase E3 Mdm2 (MDM2) is a therapeutic target for ISIS 16518. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of ISIS 16518 through regulating the expression of Ubiquitin-protein ligase E3 Mdm2 (MDM2). [89], [104]
MI-219 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Ubiquitin-protein ligase E3 Mdm2 (MDM2) is a therapeutic target for MI-219. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of MI-219 through regulating the expression of Ubiquitin-protein ligase E3 Mdm2 (MDM2). [89], [682]
NSC-66811 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Ubiquitin-protein ligase E3 Mdm2 (MDM2) is a therapeutic target for NSC-66811. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of NSC-66811 through regulating the expression of Ubiquitin-protein ligase E3 Mdm2 (MDM2). [89], [683]
NU-8231 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Ubiquitin-protein ligase E3 Mdm2 (MDM2) is a therapeutic target for NU-8231. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of NU-8231 through regulating the expression of Ubiquitin-protein ligase E3 Mdm2 (MDM2). [89], [684]
NUTLIN-3 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Ubiquitin-protein ligase E3 Mdm2 (MDM2) is a therapeutic target for NUTLIN-3. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of NUTLIN-3 through regulating the expression of Ubiquitin-protein ligase E3 Mdm2 (MDM2). [89], [685]
PLSQETFSDLWKLLPEN-NH2 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Ubiquitin-protein ligase E3 Mdm2 (MDM2) is a therapeutic target for PLSQETFSDLWKLLPEN-NH2. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of PLSQETFSDLWKLLPEN-NH2 through regulating the expression of Ubiquitin-protein ligase E3 Mdm2 (MDM2). [89], [686]
Vacuolar-type proton ATPase catalytic A (v-ATPase-A)
Cruentaren [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Vacuolar-type proton ATPase catalytic A (v-ATPase-A) is a therapeutic target for Cruentaren. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of Cruentaren through regulating the expression of Vacuolar-type proton ATPase catalytic A (v-ATPase-A). [254], [687]
References
Ref 1 Methyltransferase-like 14 silencing relieves the development of atherosclerosis via m(6)A modification of p65 mRNA. Bioengineered. 2022 May;13(5):11832-11843. doi: 10.1080/21655979.2022.2031409.
Ref 2 ABT-199, a potent and selective BCL-2 inhibitor, achieves antitumor activity while sparing platelets. Nat Med. 2013 Feb;19(2):202-8. doi: 10.1038/nm.3048. Epub 2013 Jan 6.
Ref 3 Paclitaxel directly binds to Bcl-2 and functionally mimics activity of Nur77. Cancer Res. 2009 Sep 1;69(17):6906-14.
Ref 4 Emerging therapies for multiple myeloma. Expert Opin Emerg Drugs. 2009 Mar;14(1):99-127. doi: 10.1517/14728210802676278.
Ref 5 Two concurrent phase II trials of paclitaxel/carboplatin/trastuzumab (weekly or every-3-week schedule) as first-line therapy in women with HER2-overexpressing metastatic breast cancer: NCCTG study 983252. Clin Breast Cancer. 2005 Dec;6(5):425-32. doi: 10.3816/CBC.2005.n.047.
Ref 6 Emerging disease-modifying therapies for the treatment of motor neuron disease/amyotropic lateral sclerosis. Expert Opin Emerg Drugs. 2007 May;12(2):229-52.
Ref 7 Clinical pipeline report, company report or official report of Roche (2009).
Ref 8 Multicentre phase I/II study of PI-88, a heparanase inhibitor in combination with docetaxel in patients with metastatic castrate-resistant prostate cancer. Ann Oncol. 2010 Jun;21(6):1302-1307. doi: 10.1093/annonc/mdp524. Epub 2009 Nov 16.
Ref 9 Design and optimisation of dendrimer-conjugated Bcl-2/x(L) inhibitor, AZD0466, with improved therapeutic index for cancer therapy. Commun Biol. 2021 Jan 25;4(1):112. doi: 10.1038/s42003-020-01631-8.
Ref 10 Bcl-2/Bcl-xl inhibitor APG-1252-M1 is a promising therapeutic strategy for gastric carcinoma. Cancer Med. 2020 Jun;9(12):4197-4206. doi: 10.1002/cam4.3090. Epub 2020 Apr 28.
Ref 11 Clinical pipeline report, company report or official report of ProNAi.
Ref 12 Phase II study of obatoclax mesylate (GX15-070), a small-molecule BCL-2 family antagonist, for patients with myelofibrosis. Clin Lymphoma Myeloma Leuk. 2010 Aug;10(4):285-9. doi: 10.3816/CLML.2010.n.059.
Ref 13 Apoptosis as a mechanism for the treatment of adult T cell leukemia: promising drugs from benchside to bedside. Drug Discov Today. 2020 Jul;25(7):1189-1197. doi: 10.1016/j.drudis.2020.04.023. Epub 2020 May 7.
Ref 14 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 1728).
Ref 15 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
Ref 16 National Cancer Institute Drug Dictionary (drug name LP-108).
Ref 17 A Novel BCL-2 Inhibitor APG-2575 Exerts Synthetic Lethality With BTK or MDM2-p53 Inhibitor in Diffuse Large B-Cell Lymphoma. Oncol Res. 2020 Sep 1;28(4):331-344. doi: 10.3727/096504020X15825405463920. Epub 2020 Feb 24.
Ref 18 Combination of novel imidazopyridazine mps-1 kinase inhibitors and bcl-2 family protein inhibitors. ACS Med Chem Lett. 2014 Jul 30;6(1):7-8. doi: 10.1021/ml5003037. eCollection 2015 Jan 8.
Ref 19 Inhibition of Anti-Apoptotic Bcl-2 Proteins in Preclinical and Clinical Studies: Current Overview in Cancer. Cells. 2020 May 21;9(5):1287. doi: 10.3390/cells9051287.
Ref 20 Intravenous hydrophobic drug delivery: a porous particle formulation of paclitaxel (AI-850). Pharm Res. 2005 Mar;22(3):347-55. doi: 10.1007/s11095-004-1871-1.
Ref 21 Clinical pipeline report, company report or official report of BeiGene.
Ref 22 Vaccinia virus virulence factor N1L is a novel promising target for antiviral therapeutic intervention. J Med Chem. 2010 May 27;53(10):3899-906. doi: 10.1021/jm901446n.
Ref 23 The small-molecule Bcl-2 inhibitor HA14-1 interacts synergistically with flavopiridol to induce mitochondrial injury and apoptosis in human myeloma cells through a free radical-dependent and Jun NH2-terminal kinase-dependent mechanism. Mol Cancer Ther. 2004 Dec;3(12):1513-24.
Ref 24 Structure-based design of potent small-molecule inhibitors of anti-apoptotic Bcl-2 proteins. J Med Chem. 2006 Oct 19;49(21):6139-42. doi: 10.1021/jm060460o.
Ref 25 Discovery of small-molecule inhibitors of Bcl-2 through structure-based computer screening. J Med Chem. 2001 Dec 6;44(25):4313-24. doi: 10.1021/jm010016f.
Ref 26 Design and development of antisense drugs. Expert Opin. Drug Discov. 2008 3(10):1189-1207.
Ref 27 Antitumor activity of irofulven monotherapy and in combination with mitoxantrone or docetaxel against human prostate cancer models. Prostate. 2004 Apr 1;59(1):22-32. doi: 10.1002/pros.10351.
Ref 28 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 7920).
Ref 29 Mcl-1 inhibitors: a patent review. Expert Opin Ther Pat. 2017 Feb;27(2):163-178. doi: 10.1080/13543776.2017.1249848. Epub 2016 Nov 17.
Ref 30 Dysregulated m6A modification promotes lipogenesis and development of non-alcoholic fatty liver disease and hepatocellular carcinoma. Mol Ther. 2022 Jun 1;30(6):2342-2353. doi: 10.1016/j.ymthe.2022.02.021. Epub 2022 Feb 19.
Ref 31 A liver-selective LXR inverse agonist that suppresses hepatic steatosis. ACS Chem Biol. 2013 Mar 15;8(3):559-67. doi: 10.1021/cb300541g. Epub 2012 Dec 27.
Ref 32 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2020
Ref 33 2-hydroxy-N-arylbenzenesulfonamides as ATP-citrate lyase inhibitors. Bioorg Med Chem Lett. 2007 Jun 1;17(11):3208-11. doi: 10.1016/j.bmcl.2007.03.017. Epub 2007 Mar 12.
Ref 34 N6-methyladenosine regulated FGFR4 attenuates ferroptotic cell death in recalcitrant HER2-positive breast cancer. Nat Commun. 2022 May 13;13(1):2672. doi: 10.1038/s41467-022-30217-7.
Ref 35 Discovery and preclinical evaluation of anti-miR-17 oligonucleotide RGLS4326 for the treatment of polycystic kidney disease. Nat Commun. 2019 Sep 12;10(1):4148. doi: 10.1038/s41467-019-11918-y.
Ref 36 Endostar, a modified recombinant human endostatin, suppresses angiogenesis through inhibition of Wnt/Beta-catenin signaling pathway. PLoS One. 2014 Sep 18;9(9):e107463. doi: 10.1371/journal.pone.0107463. eCollection 2014.
Ref 37 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
Ref 38 LNC942 promoting METTL14-mediated m(6)A methylation in breast cancer cell proliferation and progression. Oncogene. 2020 Jul;39(31):5358-5372. doi: 10.1038/s41388-020-1338-9. Epub 2020 Jun 23.
Ref 39 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
Ref 40 The CXCR4 Antagonist BL-8040 Efficiently Induces Apoptosis and Inhibits The Survival Of AML Cells. November 15, 2013; Blood: 122 (21).
Ref 41 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
Ref 42 Anti-ageing pipeline starts to mature. Nat Rev Drug Discov. 2018 Sep;17(9):609-612. doi: 10.1038/nrd.2018.134. Epub 2018 Aug 3.
Ref 43 Pharmacokinetic effect of AMD070, an Oral CXCR4 antagonist, on CYP3A4 and CYP2D6 substrates midazolam and dextromethorphan in healthy volunteers. J Acquir Immune Defic Syndr. 2008 Apr 15;47(5):559-65. doi: 10.1097/QAI.0b013e3181627566.
Ref 44 CXCR4 inhibitors: tumor vasculature and therapeutic challenges. Recent Pat Anticancer Drug Discov. 2012 Sep;7(3):251-64. doi: 10.2174/157489212801820039.
Ref 45 CXCR4 Antagonist TG-0054 Mobilizes Mesenchymal Stem Cells, Attenuates Inflammation, and Preserves Cardiac Systolic Function in a Porcine Model of Myocardial Infarction. Cell Transplant. 2015;24(7):1313-28. doi: 10.3727/096368914X681739. Epub 2014 May 12.
Ref 46 Beneficial effect of a CXCR4 agonist in murine models of systemic inflammation. Inflammation. 2012 Feb;35(1):130-7. doi: 10.1007/s10753-011-9297-5.
Ref 47 BMS-936564/MDX-1338: a fully human anti-CXCR4 antibody induces apoptosis in vitro and shows antitumor activity in vivo in hematologic malignancies. Clin Cancer Res. 2013 Jan 15;19(2):357-66. doi: 10.1158/1078-0432.CCR-12-2333. Epub 2012 Dec 4.
Ref 48 A CXCR4 antagonist CTCE-9908 inhibits primary tumor growth and metastasis of breast cancer. J Surg Res. 2009 Aug;155(2):231-6. doi: 10.1016/j.jss.2008.06.044. Epub 2008 Aug 9.
Ref 49 Clinical pipeline report, company report or official report of GlycoMimetics.
Ref 50 Therapeutic antibodies directed at G protein-coupled receptors. MAbs. 2010 Nov-Dec; 2(6): 594-606.
Ref 51 Inhibition of CXCR4 by LY2624587, a Fully Humanized Anti-CXCR4 Antibody Induces Apoptosis of Hematologic Malignancies. PLoS One. 2016 Mar 8;11(3):e0150585. doi: 10.1371/journal.pone.0150585. eCollection 2016.
Ref 52 CN patent application no. 101094684, With the combination of chemokine activation progenitor cells/stem cells.
Ref 53 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Target id: 71).
Ref 54 Orally bioavailable isothioureas block function of the chemokine receptor CXCR4 in vitro and in vivo. J Med Chem. 2008 Dec 25;51(24):7915-20. doi: 10.1021/jm801065q.
Ref 55 Discovery of small molecule CXCR4 antagonists. J Med Chem. 2007 Nov 15;50(23):5655-64. doi: 10.1021/jm070679i. Epub 2007 Oct 24.
Ref 56 Structure-activity relationships of cyclic peptide-based chemokine receptor CXCR4 antagonists: disclosing the importance of side-chain and backbone functionalities. J Med Chem. 2007 Jan 25;50(2):192-8. doi: 10.1021/jm0607350.
Ref 57 Progress in targeting HIV-1 entry. Drug Discov Today. 2005 Aug 15;10(16):1085-94. doi: 10.1016/S1359-6446(05)03550-6.
Ref 58 Identification of novel non-peptide CXCR4 antagonists by ligand-based design approach. Bioorg Med Chem Lett. 2008 Jul 15;18(14):4124-9. doi: 10.1016/j.bmcl.2008.05.092. Epub 2008 May 29.
Ref 59 A low-molecular-weight inhibitor against the chemokine receptor CXCR4: a strong anti-HIV peptide T140. Biochem Biophys Res Commun. 1998 Dec 30;253(3):877-82. doi: 10.1006/bbrc.1998.9871.
Ref 60 A broad-spectrum chemokine antagonist encoded by Kaposi's sarcoma-associated herpesvirus. Science. 1997 Sep 12;277(5332):1656-9. doi: 10.1126/science.277.5332.1656.
Ref 61 Noncompetitive allosteric inhibitors of the inflammatory chemokine receptors CXCR1 and CXCR2: prevention of reperfusion injury. Proc Natl Acad Sci U S A. 2004 Aug 10;101(32):11791-6. doi: 10.1073/pnas.0402090101. Epub 2004 Jul 28.
Ref 62 Suradista NSC 651016 inhibits the angiogenic activity of CXCL12-stromal cell-derived factor 1alpha. Clin Cancer Res. 2002 Dec;8(12):3955-60.
Ref 63 Caspase-dependent apoptosis of cells expressing the chemokine receptor CXCR4 is induced by cell membrane-associated human immunodeficiency virus type 1 envelope glycoprotein (gp120). Virology. 2000 Mar 15;268(2):329-44. doi: 10.1006/viro.1999.0151.
Ref 64 Comparative evaluation of CC chemokine-induced migration of murine CD8alpha+ and CD8alpha- dendritic cells and their in vivo trafficking. J Leukoc Biol. 2004 Feb;75(2):275-85. doi: 10.1189/jlb.1202613. Epub 2003 Nov 3.
Ref 65 m(6) A RNA methyltransferases METTL3/14 regulate immune responses to anti-PD-1 therapy. EMBO J. 2020 Oct 15;39(20):e104514. doi: 10.15252/embj.2020104514. Epub 2020 Sep 23.
Ref 66 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800029267)
Ref 67 Antitumor efficacy of a thrombospondin 1 mimetic CovX-body. Transl Oncol. 2011 Aug;4(4):249-57. doi: 10.1593/tlo.11136. Epub 2011 Aug 1.
Ref 68 Anti-IP-10 antibody (BMS-936557) for ulcerative colitis: a phase II randomised study. Gut. 2014 Mar;63(3):442-50. doi: 10.1136/gutjnl-2012-303424. Epub 2013 Mar 5.
Ref 69 A phase II, randomized, double-blind, placebo-controlled study evaluating the efficacy and safety of MDX-1100, a fully human anti-CXCL10 monoclonal antibody, in combination with methotrexate in patients with rheumatoid arthritis. Arthritis Rheum. 2012 Jun;64(6):1730-9. doi: 10.1002/art.34330. Epub 2011 Dec 6.
Ref 70 Clinical pipeline report, company report or official report of PsiOxus Therapeutics.
Ref 71 The anti-inflammatory mechanism of sulfasalazine is related to adenosine release at inflamed sites. J Immunol. 1996 Mar 1;156(5):1937-41.
Ref 72 METTL14 Inhibits Hematopoietic Stem/Progenitor Differentiation and Promotes Leukemogenesis via mRNA m(6)A Modification. Cell Stem Cell. 2018 Feb 1;22(2):191-205.e9. doi: 10.1016/j.stem.2017.11.016. Epub 2017 Dec 28.
Ref 73 US patent application no. 6,271,030, Antisense inhibition of C/EBP beta expression.
Ref 74 US patent application no. 6,238,921, Antisense oligonucleotide modulation of human mdm2 expression.
Ref 75 m(6)A mRNA methylation regulates testosterone synthesis through modulating autophagy in Leydig cells. Autophagy. 2021 Feb;17(2):457-475. doi: 10.1080/15548627.2020.1720431. Epub 2020 Jan 31.
Ref 76 7,8-dichloro-1-oxo-Beta-carbolines as a versatile scaffold for the development of potent and selective kinase inhibitors with unusual binding modes. J Med Chem. 2012 Jan 12;55(1):403-13. doi: 10.1021/jm201286z. Epub 2012 Jan 3.
Ref 77 METTL14 Overexpression Promotes Osteosarcoma Cell Apoptosis and Slows Tumor Progression via Caspase 3 Activation. Cancer Manag Res. 2020 Dec 11;12:12759-12767. doi: 10.2147/CMAR.S284273. eCollection 2020.
Ref 78 4-Alkoxy-2,6-diaminopyrimidine derivatives: inhibitors of cyclin dependent kinases 1 and 2. Bioorg Med Chem Lett. 2003 Jan 20;13(2):217-22. doi: 10.1016/s0960-894x(02)00884-3.
Ref 79 Design, synthesis, and biological evaluation of isoquinoline-1,3,4-trione derivatives as potent caspase-3 inhibitors. J Med Chem. 2006 Mar 9;49(5):1613-23. doi: 10.1021/jm050896o.
Ref 80 Design, synthesis, and discovery of novel non-peptide inhibitor of Caspase-3 using ligand based and structure based virtual screening approach. Bioorg Med Chem. 2009 Aug 15;17(16):6040-7. doi: 10.1016/j.bmc.2009.06.069. Epub 2009 Jul 7.
Ref 81 Synthesis and evaluation of vinyl sulfones as caspase-3 inhibitors. A structure-activity study. Eur J Med Chem. 2010 Sep;45(9):3858-63. doi: 10.1016/j.ejmech.2010.05.039. Epub 2010 May 24.
Ref 82 Small-molecule activation of procaspase-3 to caspase-3 as a personalized anticancer strategy. Nat Chem Biol. 2006 Oct;2(10):543-50. doi: 10.1038/nchembio814. Epub 2006 Aug 27.
Ref 83 Design and synthesis of a potent and selective peptidomimetic inhibitor of caspase-3. J Med Chem. 2004 Dec 16;47(26):6455-8. doi: 10.1021/jm049248f.
Ref 84 Distinctive roles of PHAP proteins and prothymosin-alpha in a death regulatory pathway. Science. 2003 Jan 10;299(5604):223-6. doi: 10.1126/science.1076807.
Ref 85 Novel small molecule inhibitors of caspase-3 block cellular and biochemical features of apoptosis. J Pharmacol Exp Ther. 2003 Jan;304(1):433-40. doi: 10.1124/jpet.102.039651.
Ref 86 Novel pyrazinone mono-amides as potent and reversible caspase-3 inhibitors. Bioorg Med Chem Lett. 2005 Feb 15;15(4):1173-80. doi: 10.1016/j.bmcl.2004.12.006.
Ref 87 Glionitrin A, a new diketopiperazine disulfide, activates ATM-ATR-Chk1/2 via 53BP1 phosphorylation in DU145 cells and shows antitumor effect in xenograft model. Biol Pharm Bull. 2014;37(3):378-86. doi: 10.1248/bpb.b13-00719.
Ref 88 The selective class I PI3K inhibitor CH5132799 targets human cancers harboring oncogenic PIK3CA mutations. Clin Cancer Res. 2011 May 15;17(10):3272-81. doi: 10.1158/1078-0432.CCR-10-2882. Epub 2011 May 10.
Ref 89 The m(6)A RNA methyltransferase METTL3/METTL14 promotes leukemogenesis through the mdm2/p53 pathway in acute myeloid leukemia. J Cancer. 2022 Jan 4;13(3):1019-1030. doi: 10.7150/jca.60381. eCollection 2022.
Ref 90 Interpreting expression profiles of cancers by genome-wide survey of breadth of expression in normal tissues. Genomics. 2005 Aug;86(2):127-41. doi: 10.1016/j.ygeno.2005.04.008.
Ref 91 Comparison of Antitumor Effects of Combined and Separate Treatment with NO Synthase Inhibitor T1023 and PDK1 Inhibitor Dichloroacetate. Bull Exp Biol Med. 2019 Nov;168(1):92-94. doi: 10.1007/s10517-019-04655-1. Epub 2019 Nov 25.
Ref 92 A review of contusugene ladenovec (Advexin) p53 therapy. Curr Opin Mol Ther. 2009 Feb;11(1):54-61.
Ref 93 Transferrin receptor targeting nanomedicine delivering wild-type p53 gene sensitizes pancreatic cancer to gemcitabine therapy. Cancer Gene Ther. 2013 Apr;20(4):222-8. doi: 10.1038/cgt.2013.9. Epub 2013 Mar 8.
Ref 94 INGN-225: a dendritic cell-based p53 vaccine (Ad.p53-DC) in small cell lung cancer: observed association between immune response and enhanced chemotherapy effect. Expert Opin Biol Ther. 2010 Jun;10(6):983-91. doi: 10.1517/14712598.2010.484801.
Ref 95 Phase I trial of ALT-801, an interleukin-2/T-cell receptor fusion protein targeting p53 (aa264-272)/HLA-A*0201 complex, in patients with advanced malignancies. Clin Cancer Res. 2011 Dec 15;17(24):7765-75. doi: 10.1158/1078-0432.CCR-11-1817. Epub 2011 Oct 12.
Ref 96 The Protein Data Bank. Nucleic Acids Res. 2000 Jan 1;28(1):235-42. doi: 10.1093/nar/28.1.235.
Ref 97 STO-609, a specific inhibitor of the Ca(2+)/calmodulin-dependent protein kinase kinase. J Biol Chem. 2002 May 3;277(18):15813-8. doi: 10.1074/jbc.M201075200. Epub 2002 Feb 26.
Ref 98 Assessment of p53 gene transfer and biological activities in a clinical study of adenovirus-p53 gene therapy for recurrent ovarian cancer. Cancer Gene Ther. 2003 Mar;10(3):224-38. doi: 10.1038/sj.cgt.7700562.
Ref 99 Phase 2 randomized study of p53 antisense oligonucleotide (cenersen) plus idarubicin with or without cytarabine in refractory and relapsed acute myeloid leukemia. Cancer. 2012 Jan 15;118(2):418-27. doi: 10.1002/cncr.26292. Epub 2011 Jun 29.
Ref 100 WO patent application no. 2013,1850,32, Nanotherapeutics for drug targeting.
Ref 101 National Cancer Institute Drug Dictionary (drug id 761551).
Ref 102 Late viral RNA export, rather than p53 inactivation, determines ONYX-015 tumor selectivity. Cancer Cell. 2004 Dec;6(6):611-23. doi: 10.1016/j.ccr.2004.11.012.
Ref 103 SAR405838: an optimized inhibitor of MDM2-p53 interaction that induces complete and durable tumor regression. Cancer Res. 2014 Oct 15;74(20):5855-65. doi: 10.1158/0008-5472.CAN-14-0799. Epub 2014 Aug 21.
Ref 104 Small-molecule inhibitors of the MDM2-p53 protein-protein interaction based on an isoindolinone scaffold. J Med Chem. 2006 Oct 19;49(21):6209-21. doi: 10.1021/jm0601194.
Ref 105 2011 Pipeline of Quark Pharm.
Ref 106 Discovery and optimization of chromenotriazolopyrimidines as potent inhibitors of the mouse double minute 2-tumor protein 53 protein-protein interaction. J Med Chem. 2009 Nov 26;52(22):7044-53. doi: 10.1021/jm900681h.
Ref 107 An evaluation of the ability of pifithrin-alpha and -beta to inhibit p53 function in two wild-type p53 human tumor cell lines. Mol Cancer Ther. 2005 Sep;4(9):1369-77. doi: 10.1158/1535-7163.MCT-04-0341.
Ref 108 Vaccination with p53-peptide-pulsed dendritic cells, of patients with advanced breast cancer: report from a phase I study. Cancer Immunol Immunother. 2004 Jul;53(7):633-41. doi: 10.1007/s00262-003-0493-5. Epub 2004 Feb 25.
Ref 109 Regulation of host gene expression by HIV-1 TAR microRNAs. Retrovirology. 2013; 10: 86.
Ref 110 Prevent Oral Cancer With Mouthwash. Introgen Therapeutics.
Ref 111 The glutamate/cystine antiporter SLC7A11/xCT enhances cancer cell dependency on glucose by exporting glutamate. J Biol Chem. 2017 Aug 25;292(34):14240-14249. doi: 10.1074/jbc.M117.798405. Epub 2017 Jun 19.
Ref 112 US patent application no. 6,498,035, Antisense modulation of MEKK3 expression.
Ref 113 Amodiaquine clearance and its metabolism to N-desethylamodiaquine is mediated by CYP2C8: a new high affinity and turnover enzyme-specific probe substrate. J Pharmacol Exp Ther. 2002 Feb;300(2):399-407. doi: 10.1124/jpet.300.2.399.
Ref 114 Oxidation of xenobiotics by recombinant human cytochrome P450 1B1. Drug Metab Dispos. 1997 May;25(5):617-22.
Ref 115 Cytochromes P450 in crustacea. Comp Biochem Physiol C Pharmacol Toxicol Endocrinol. 1998 Nov;121(1-3):157-72. doi: 10.1016/s0742-8413(98)10036-1.
Ref 116 A common CYP1B1 polymorphism is associated with 2-OHE1/16-OHE1 urinary estrone ratio. Clin Chem Lab Med. 2005;43(7):702-6. doi: 10.1515/CCLM.2005.119.
Ref 117 Human CYP1B1 and anticancer agent metabolism: mechanism for tumor-specific drug inactivation?. J Pharmacol Exp Ther. 2001 Feb;296(2):537-41.
Ref 118 NADPH- and hydroperoxide-supported 17beta-estradiol hydroxylation catalyzed by a variant form (432L, 453S) of human cytochrome P450 1B1. J Steroid Biochem Mol Biol. 2000 Sep;74(1-2):11-8. doi: 10.1016/s0960-0760(00)00083-2.
Ref 119 Metabolism of melatonin by human cytochromes p450. Drug Metab Dispos. 2005 Apr;33(4):489-94. doi: 10.1124/dmd.104.002410. Epub 2004 Dec 22.
Ref 120 The influence of metabolic gene polymorphisms on urinary 1-hydroxypyrene concentrations in Chinese coke oven workers. Sci Total Environ. 2007 Aug 1;381(1-3):38-46. doi: 10.1016/j.scitotenv.2007.02.021. Epub 2007 May 11.
Ref 121 Tumour cytochrome P450 and drug activation. Curr Pharm Des. 2002;8(15):1335-47. doi: 10.2174/1381612023394502.
Ref 122 Catalytic properties of polymorphic human cytochrome P450 1B1 variants. Carcinogenesis. 1999 Aug;20(8):1607-13. doi: 10.1093/carcin/20.8.1607.
Ref 123 Pharmacokinetics of rosuvastatin when coadministered with rifampicin in healthy males: a randomized, single-blind, placebo-controlled, crossover study. Clin Ther. 2008 Jul;30(7):1283-9. doi: 10.1016/s0149-2918(08)80052-5.
Ref 124 Cytochrome P450 isoforms catalyze formation of catechol estrogen quinones that react with DNA. Metabolism. 2007 Jul;56(7):887-94. doi: 10.1016/j.metabol.2007.03.001.
Ref 125 Cytochrome P450 CYP1B1 interacts with 8-methoxypsoralen (8-MOP) and influences psoralen-ultraviolet A (PUVA) sensitivity. PLoS One. 2013 Sep 23;8(9):e75494. doi: 10.1371/journal.pone.0075494. eCollection 2013.
Ref 126 Metabolism of retinoids and arachidonic acid by human and mouse cytochrome P450 1b1. Drug Metab Dispos. 2004 Aug;32(8):840-7. doi: 10.1124/dmd.32.8.840.
Ref 127 US patent application no. 6,277,636, Antisense inhibition of MADH6 expression.
Ref 128 Selective inhibition of methoxyflavonoids on human CYP1B1 activity. Bioorg Med Chem. 2010 Sep 1;18(17):6310-5. doi: 10.1016/j.bmc.2010.07.020. Epub 2010 Jul 13.
Ref 129 Design, synthesis, and discovery of novel trans-stilbene analogues as potent and selective human cytochrome P450 1B1 inhibitors. J Med Chem. 2002 Jan 3;45(1):160-4. doi: 10.1021/jm010298j.
Ref 130 Inhibition of human cytochrome p450 1b1 further clarifies its role in the activation of dibenzo[a,l]pyrene in cells in culture. J Biochem Mol Toxicol. 2007;21(3):101-9. doi: 10.1002/jbt.20168.
Ref 131 Methylation of adenosine at the N(6) position post-transcriptionally regulates hepatic P450s expression. Biochem Pharmacol. 2020 Jan;171:113697. doi: 10.1016/j.bcp.2019.113697. Epub 2019 Nov 7.
Ref 132 Identification of the human liver enzymes involved in the metabolism of the antimigraine agent almotriptan. Drug Metab Dispos. 2003 Apr;31(4):404-11. doi: 10.1124/dmd.31.4.404.
Ref 133 Contribution of human hepatic cytochrome P450s and steroidogenic CYP17 to the N-demethylation of aminopyrine. Xenobiotica. 1999 Feb;29(2):187-93. doi: 10.1080/004982599238731.
Ref 134 Functional characterization of five novel CYP2C8 variants, G171S, R186X, R186G, K247R, and K383N, found in a Japanese population. Drug Metab Dispos. 2005 May;33(5):630-6. doi: 10.1124/dmd.105.003830. Epub 2005 Feb 16.
Ref 135 The xenobiotic inhibitor profile of cytochrome P4502C8. Br J Clin Pharmacol. 2000 Dec;50(6):573-80. doi: 10.1046/j.1365-2125.2000.00316.x.
Ref 136 Amodiaquine metabolism is impaired by common polymorphisms in CYP2C8: implications for malaria treatment in Africa. Clin Pharmacol Ther. 2007 Aug;82(2):197-203. doi: 10.1038/sj.clpt.6100122. Epub 2007 Mar 14.
Ref 137 In vitro and in vivo oxidative metabolism and glucuronidation of anastrozole. Br J Clin Pharmacol. 2010 Dec;70(6):854-69. doi: 10.1111/j.1365-2125.2010.03791.x.
Ref 138 Apalutamide: First Global Approval. Drugs. 2018 Apr;78(6):699-705. doi: 10.1007/s40265-018-0900-z.
Ref 139 Apixaban. Hosp Pharm. 2013 Jun;48(6):494-509. doi: 10.1310/hpj4806-494.
Ref 140 Role of Cytochrome P450 2C8 in Drug Metabolism and Interactions. Pharmacol Rev. 2016 Jan;68(1):168-241. doi: 10.1124/pr.115.011411.
Ref 141 Azelastine N-demethylation by cytochrome P-450 (CYP)3A4, CYP2D6, and CYP1A2 in human liver microsomes: evaluation of approach to predict the contribution of multiple CYPs. Drug Metab Dispos. 1999 Dec;27(12):1381-91.
Ref 142 Cytochrome P450 isozymes responsible for the metabolism of toluene and styrene in human liver microsomes. Xenobiotica. 1997 Jul;27(7):657-65. doi: 10.1080/004982597240253.
Ref 143 Evaluation of drug-drug interaction potential of beraprost sodium mediated by P450 in vitro. Yakugaku Zasshi. 2008 Oct;128(10):1459-65. doi: 10.1248/yakushi.128.1459.
Ref 144 Brigatinib: First Global Approval. Drugs. 2017 Jul;77(10):1131-1135. doi: 10.1007/s40265-017-0776-3.
Ref 145 Metabolite Profiling and Reaction Phenotyping for the in Vitro Assessment of the Bioactivation of Bromfenac ?. Chem Res Toxicol. 2020 Jan 21;33(1):249-257. doi: 10.1021/acs.chemrestox.9b00268. Epub 2019 Dec 23.
Ref 146 Buprenorphine in cancer pain. Support Care Cancer. 2005 Nov;13(11):878-87. doi: 10.1007/s00520-005-0849-9. Epub 2005 Jul 12.
Ref 147 DAILYMED.nlm.nih.gov: JEVTANA- cabazitaxel kit.
Ref 148 PharmGKB summary: caffeine pathway. Pharmacogenet Genomics. 2012 May;22(5):389-95. doi: 10.1097/FPC.0b013e3283505d5e.
Ref 149 Metabolism of capsaicin by cytochrome P450 produces novel dehydrogenated metabolites and decreases cytotoxicity to lung and liver cells. Chem Res Toxicol. 2003 Mar;16(3):336-49. doi: 10.1021/tx025599q.
Ref 150 Potential interaction between ritonavir and carbamazepine. Pharmacotherapy. 2000 Jul;20(7):851-4. doi: 10.1592/phco.20.9.851.35206.
Ref 151 Gemfibrozil and its glucuronide inhibit the organic anion transporting polypeptide 2 (OATP2/OATP1B1:SLC21A6)-mediated hepatic uptake and CYP2C8-mediated metabolism of cerivastatin: analysis of the mechanism of the clinically relevant drug-drug interaction between cerivastatin and gemfibrozil. J Pharmacol Exp Ther. 2004 Oct;311(1):228-36. doi: 10.1124/jpet.104.068536. Epub 2004 Jun 11.
Ref 152 Cytochrome P450 2C8 pharmacogenetics: a review of clinical studies. Pharmacogenomics. 2009 Sep;10(9):1489-510. doi: 10.2217/pgs.09.82.
Ref 153 Interaction of cisapride with the human cytochrome P450 system: metabolism and inhibition studies. Drug Metab Dispos. 2000 Jul;28(7):789-800.
Ref 154 Elucidation of individual cytochrome P450 enzymes involved in the metabolism of clozapine. Naunyn Schmiedebergs Arch Pharmacol. 1998 Nov;358(5):592-9. doi: 10.1007/pl00005298.
Ref 155 Enhanced cyclophosphamide and ifosfamide activation in primary human hepatocyte cultures: response to cytochrome P-450 inducers and autoinduction by oxazaphosphorines. Cancer Res. 1997 May 15;57(10):1946-54.
Ref 156 CYP2C8/9 mediate dapsone N-hydroxylation at clinical concentrations of dapsone. Drug Metab Dispos. 2000 Aug;28(8):865-8.
Ref 157 Further Characterization of the Metabolism of Desloratadine and Its Cytochrome P450 and UDP-glucuronosyltransferase Inhibition Potential: Identification of Desloratadine as a Relatively Selective UGT2B10 Inhibitor. Drug Metab Dispos. 2015 Sep;43(9):1294-302. doi: 10.1124/dmd.115.065011. Epub 2015 Jul 1.
Ref 158 Influence of CYP2C8 polymorphisms on the hydroxylation metabolism of paclitaxel, repaglinide and ibuprofen enantiomers in vitro. Biopharm Drug Dispos. 2013 Jul;34(5):278-87. doi: 10.1002/bdd.1842. Epub 2013 Jun 3.
Ref 159 Use of inhibitory monoclonal antibodies to assess the contribution of cytochromes P450 to human drug metabolism. Eur J Pharmacol. 2000 Apr 14;394(2-3):199-209. doi: 10.1016/s0014-2999(00)00079-0.
Ref 160 Analysis of human cytochrome P450 2C8 substrate specificity using a substrate pharmacophore and site-directed mutants. Biochemistry. 2004 Dec 14;43(49):15379-92. doi: 10.1021/bi0489309.
Ref 161 Reversible inhibition of four important human liver cytochrome P450 enzymes by diethylstilbestrol. Pharmazie. 2011 Mar;66(3):216-21.
Ref 162 Role of CYP3A4 in human hepatic diltiazem N-demethylation: inhibition of CYP3A4 activity by oxidized diltiazem metabolites. J Pharmacol Exp Ther. 1997 Jul;282(1):294-300.
Ref 163 Eltrombopag-Induced Acute Liver Failure in a Pediatric Patient: A Pharmacokinetic and Pharmacogenetic Analysis. Ther Drug Monit. 2018 Aug;40(4):386-388. doi: 10.1097/FTD.0000000000000522.
Ref 164 FDA Label of Enasidenib. The 2020 official website of the U.S. Food and Drug Administration.
Ref 165 Role of cytochrome P450 in estradiol metabolism in vitro. Acta Pharmacol Sin. 2001 Feb;22(2):148-54.
Ref 166 Substrates, inducers, inhibitors and structure-activity relationships of human Cytochrome P450 2C9 and implications in drug development. Curr Med Chem. 2009;16(27):3480-675. doi: 10.2174/092986709789057635. Epub 2009 Sep 1.
Ref 167 Examination of 209 drugs for inhibition of cytochrome P450 2C8. J Clin Pharmacol. 2005 Jan;45(1):68-78. doi: 10.1177/0091270004270642.
Ref 168 Comparison of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors (statins) as inhibitors of cytochrome P450 2C8. Basic Clin Pharmacol Toxicol. 2005 Aug;97(2):104-8. doi: 10.1111/j.1742-7843.2005.pto_134.x.
Ref 169 Metabolism, excretion and pharmacokinetics of [(14)C]glasdegib (PF-04449913) in healthy volunteers following oral administration. Xenobiotica. 2017 Dec;47(12):1064-1076. doi: 10.1080/00498254.2016.1261307. Epub 2017 Jan 3.
Ref 170 Halofantrine metabolism in microsomes in man: major role of CYP 3A4 and CYP 3A5. J Pharm Pharmacol. 1999 Apr;51(4):419-26. doi: 10.1211/0022357991772628.
Ref 171 Effects of Rifampin on the Pharmacokinetics of a Single Dose of Istradefylline in Healthy Subjects. J Clin Pharmacol. 2018 Feb;58(2):193-201. doi: 10.1002/jcph.1003. Epub 2017 Sep 7.
Ref 172 Ninlaro- European Medicines Agency - European Union
Ref 173 Ketobemidone is a substrate for cytochrome P4502C9 and 3A4, but not for P-glycoprotein. Xenobiotica. 2005 Aug;35(8):785-96. doi: 10.1080/00498250500183181.
Ref 174 Body weight, gender and pregnancy affect enantiomer-specific ketorolac pharmacokinetics. Br J Clin Pharmacol. 2017 Sep;83(9):1966-1975. doi: 10.1111/bcp.13311. Epub 2017 May 14.
Ref 175 Identification of the human P450 enzymes involved in lansoprazole metabolism. J Pharmacol Exp Ther. 1996 May;277(2):805-16.
Ref 176 Mechanism-based inactivation of cytochrome P450 3A4 by lapatinib. Mol Pharmacol. 2010 Oct;78(4):693-703. doi: 10.1124/mol.110.065839. Epub 2010 Jul 12.
Ref 177 The Role of Levomilnacipran in the Management of Major Depressive Disorder: A Comprehensive Review. Curr Neuropharmacol. 2016;14(2):191-9. doi: 10.2174/1570159x14666151117122458.
Ref 178 Summary of information on human CYP enzymes: human P450 metabolism data. Drug Metab Rev. 2002 Feb-May;34(1-2):83-448. doi: 10.1081/dmr-120001392.
Ref 179 Identification of cytochrome P450 isoforms involved in the metabolism of loperamide in human liver microsomes. Eur J Clin Pharmacol. 2004 Oct;60(8):575-81. doi: 10.1007/s00228-004-0815-3. Epub 2004 Sep 8.
Ref 180 FDA label of Lorlatinib. The 2020 official website of the U.S. Food and Drug Administration.
Ref 181 Drug-drug Interaction between Losartan and Paclitaxel in Human Liver Microsomes with Different CYP2C8 Genotypes. Basic Clin Pharmacol Toxicol. 2015 Jun;116(6):493-8. doi: 10.1111/bcpt.12355. Epub 2014 Dec 23.
Ref 182 Pharmacogenomics of statins: understanding susceptibility to adverse effects. Pharmgenomics Pers Med. 2016 Oct 3;9:97-106. doi: 10.2147/PGPM.S86013. eCollection 2016.
Ref 183 Genetically based impairment in CYP2C8- and CYP2C9-dependent NSAID metabolism as a risk factor for gastrointestinal bleeding: is a combination of pharmacogenomics and metabolomics required to improve personalized medicine?. Expert Opin Drug Metab Toxicol. 2009 Jun;5(6):607-20. doi: 10.1517/17425250902970998.
Ref 184 Evidence that CYP2C19 is the major (S)-mephenytoin 4'-hydroxylase in humans. Biochemistry. 1994 Feb 22;33(7):1743-52. doi: 10.1021/bi00173a017.
Ref 185 Loss of orally administered drugs in GI tract. Saudi Pharm J. 2012 Oct;20(4):331-44. doi: 10.1016/j.jsps.2012.03.005. Epub 2012 Apr 20.
Ref 186 Methadone Metabolism and Drug-Drug Interactions: In?Vitro and In?Vivo Literature Review. J Pharm Sci. 2018 Dec;107(12):2983-2991. doi: 10.1016/j.xphs.2018.08.025. Epub 2018 Sep 8.
Ref 187 Determinants of cytochrome P450 2C8 substrate binding: structures of complexes with montelukast, troglitazone, felodipine, and 9-cis-retinoic acid. J Biol Chem. 2008 Jun 20;283(25):17227-37. doi: 10.1074/jbc.M802180200. Epub 2008 Apr 15.
Ref 188 In vitro metabolism study of buprenorphine: evidence for new metabolic pathways. Drug Metab Dispos. 2005 May;33(5):689-95. doi: 10.1124/dmd.105.003681. Epub 2005 Mar 2.
Ref 189 PharmGKB summary: mycophenolic acid pathway. Pharmacogenet Genomics. 2014 Jan;24(1):73-9. doi: 10.1097/FPC.0000000000000010.
Ref 190 Involvement of multiple cytochrome P450 isoforms in naproxen O-demethylation. Eur J Clin Pharmacol. 1997;52(4):293-8. doi: 10.1007/s002280050293.
Ref 191 Roles of CYP2A6 and CYP2B6 in nicotine C-oxidation by human liver microsomes. Arch Toxicol. 1999 Mar;73(2):65-70. doi: 10.1007/s002040050588.
Ref 192 Metabolism and Disposition of Pan-Genotypic Inhibitor of Hepatitis C Virus NS5A Ombitasvir in Humans. Drug Metab Dispos. 2016 Aug;44(8):1148-57. doi: 10.1124/dmd.115.067496. Epub 2016 May 13.
Ref 193 Human CYP2C19 is a major omeprazole 5-hydroxylase, as demonstrated with recombinant cytochrome P450 enzymes. Drug Metab Dispos. 1996 Oct;24(10):1081-7.
Ref 194 Pazopanib, a new therapy for metastatic soft tissue sarcoma. Expert Opin Pharmacother. 2013 May;14(7):929-35. doi: 10.1517/14656566.2013.780030. Epub 2013 Mar 14.
Ref 195 Identification of human cytochrome P(450)s that metabolise anti-parasitic drugs and predictions of in vivo drug hepatic clearance from in vitro data. Eur J Clin Pharmacol. 2003 Sep;59(5-6):429-42. doi: 10.1007/s00228-003-0636-9. Epub 2003 Aug 12.
Ref 196 Identification of the human cytochrome P450 isoforms mediating in vitro N-dealkylation of perphenazine. Br J Clin Pharmacol. 2000 Dec;50(6):563-71. doi: 10.1046/j.1365-2125.2000.00298.x.
Ref 197 Colchicine down-regulates cytochrome P450 2B6, 2C8, 2C9, and 3A4 in human hepatocytes by affecting their glucocorticoid receptor-mediated regulation. Mol Pharmacol. 2003 Jul;64(1):160-9. doi: 10.1124/mol.64.1.160.
Ref 198 Identification of cytochromes P450 2C9 and 3A4 as the major catalysts of phenprocoumon hydroxylation in vitro. Eur J Clin Pharmacol. 2004 May;60(3):173-82. doi: 10.1007/s00228-004-0740-5. Epub 2004 Mar 31.
Ref 199 The role of human CYP2C8 and CYP2C9 variants in pioglitazone metabolism in vitro. Basic Clin Pharmacol Toxicol. 2009 Dec;105(6):374-9. doi: 10.1111/j.1742-7843.2009.00457.x. Epub 2009 Jul 15.
Ref 200 Efficacy of piroxicam for postoperative pain after lower third molar surgery associated with CYP2C8*3 and CYP2C9. J Pain Res. 2017 Jul 6;10:1581-1589. doi: 10.2147/JPR.S138147. eCollection 2017.
Ref 201 Comparison of the safety, tolerability, and pharmacokinetic profile of a single oral dose of pitavastatin 4 mg in adult subjects with severe renal impairment not on hemodialysis versus healthy adult subjects. J Cardiovasc Pharmacol. 2012 Jul;60(1):42-8. doi: 10.1097/FJC.0b013e318256cdf0.
Ref 202 Possible involvement of multiple human cytochrome P450 isoforms in the liver metabolism of propofol. Br J Anaesth. 1998 Jun;80(6):788-95. doi: 10.1093/bja/80.6.788.
Ref 203 Drug-drug and food-drug pharmacokinetic interactions with new insulinotropic agents repaglinide and nateglinide. Clin Pharmacokinet. 2007;46(2):93-108. doi: 10.2165/00003088-200746020-00001.
Ref 204 Riociguat (adempas): a novel agent for the treatment of pulmonary arterial hypertension and chronic thromboembolic pulmonary hypertension. P T. 2014 Nov;39(11):749-58.
Ref 205 Characterization of the cytochrome P450 enzymes involved in the in vitro metabolism of rosiglitazone. Br J Clin Pharmacol. 1999 Sep;48(3):424-32. doi: 10.1046/j.1365-2125.1999.00030.x.
Ref 206 Comparative studies on the cytochrome p450-associated metabolism and interaction potential of selegiline between human liver-derived in vitro systems. Drug Metab Dispos. 2003 Sep;31(9):1093-102. doi: 10.1124/dmd.31.9.1093.
Ref 207 FDA Label of Uptravi. The 2020 official website of the U.S. Food and Drug Administration.
Ref 208 Drug interactions with lipid-lowering drugs: mechanisms and clinical relevance. Clin Pharmacol Ther. 2006 Dec;80(6):565-81. doi: 10.1016/j.clpt.2006.09.003.
Ref 209 Pharmacokinetics of dipeptidylpeptidase-4 inhibitors. Diabetes Obes Metab. 2010 Aug;12(8):648-58. doi: 10.1111/j.1463-1326.2010.01212.x.
Ref 210 Reduction of sulfamethoxazole and dapsone hydroxylamines by a microsomal enzyme system purified from pig liver and pig and human liver microsomes. Life Sci. 2005 May 27;77(2):205-19. doi: 10.1016/j.lfs.2004.12.028. Epub 2005 Feb 8.
Ref 211 Sulfamethoxazole and its metabolite nitroso sulfamethoxazole stimulate dendritic cell costimulatory signaling. J Immunol. 2007 May 1;178(9):5533-42. doi: 10.4049/jimmunol.178.9.5533.
Ref 212 Cytochrome P450 2C8 and flavin-containing monooxygenases are involved in the metabolism of tazarotenic acid in humans. Drug Metab Dispos. 2003 Apr;31(4):476-81. doi: 10.1124/dmd.31.4.476.
Ref 213 Roles of cytochromes P450 1A2, 2A6, and 2C8 in 5-fluorouracil formation from tegafur, an anticancer prodrug, in human liver microsomes. Drug Metab Dispos. 2000 Dec;28(12):1457-63.
Ref 214 Human liver microsomal diazepam metabolism using cDNA-expressed cytochrome P450s: role of CYP2B6, 2C19 and the 3A subfamily. Xenobiotica. 1996 Nov;26(11):1155-66. doi: 10.3109/00498259609050260.
Ref 215 Thalidomide metabolism by the CYP2C subfamily. Clin Cancer Res. 2002 Jun;8(6):1964-73.
Ref 216 Prediction of in vivo drug-drug interactions between tolbutamide and various sulfonamides in humans based on in vitro experiments. Drug Metab Dispos. 2000 Apr;28(4):475-81.
Ref 217 Mechanism-based inactivation of human cytochrome P4502C8 by drugs in vitro. J Pharmacol Exp Ther. 2004 Dec;311(3):996-1007. doi: 10.1124/jpet.104.071803. Epub 2004 Aug 10.
Ref 218 FDA label of Treprostinil. The 2020 official website of the U.S. Food and Drug Administration.
Ref 219 FDA label of Trifarotene. The 2020 official website of the U.S. Food and Drug Administration.
Ref 220 Trimethadione metabolism by human liver cytochrome P450: evidence for the involvement of CYP2E1. Xenobiotica. 1998 Nov;28(11):1041-7. doi: 10.1080/004982598238930.
Ref 221 Pioglitazone is metabolised by CYP2C8 and CYP3A4 in vitro: potential for interactions with CYP2C8 inhibitors. Basic Clin Pharmacol Toxicol. 2006 Jul;99(1):44-51. doi: 10.1111/j.1742-7843.2006.pto_437.x.
Ref 222 Effect of genetic polymorphisms in cytochrome p450 (CYP) 2C9 and CYP2C8 on the pharmacokinetics of oral antidiabetic drugs: clinical relevance. Clin Pharmacokinet. 2005;44(12):1209-25. doi: 10.2165/00003088-200544120-00002.
Ref 223 FDA Label of Vosevi. The 2020 official website of the U.S. Food and Drug Administration.
Ref 224 Differential expression and function of CYP2C isoforms in human intestine and liver. Pharmacogenetics. 2003 Sep;13(9):565-75. doi: 10.1097/00008571-200309000-00005.
Ref 225 Identification of the cytochrome P450 and other enzymes involved in the in vitro oxidative metabolism of a novel antidepressant, Lu AA21004. Drug Metab Dispos. 2012 Jul;40(7):1357-65. doi: 10.1124/dmd.112.044610. Epub 2012 Apr 11.
Ref 226 Cytochrome P-450 3A4 and 2C8 are involved in zopiclone metabolism. Drug Metab Dispos. 1999 Sep;27(9):1068-73.
Ref 227 Involvement of multiple cytochrome P450 and UDP-glucuronosyltransferase enzymes in the in vitro metabolism of muraglitazar. Drug Metab Dispos. 2007 Jan;35(1):139-49. doi: 10.1124/dmd.106.011932. Epub 2006 Oct 24.
Ref 228 Evaluation of in vitro drug interactions with karenitecin, a novel, highly lipophilic camptothecin derivative in phase II clinical development. J Clin Pharmacol. 2003 Sep;43(9):1008-14. doi: 10.1177/0091270003255921.
Ref 229 Effects of gemfibrozil, itraconazole, and their combination on the pharmacokinetics of pioglitazone. Clin Pharmacol Ther. 2005 May;77(5):404-14. doi: 10.1016/j.clpt.2004.12.266.
Ref 230 Pharmacokinetics and Disposition of Momelotinib Revealed a Disproportionate Human Metabolite-Resolution for Clinical Development. Drug Metab Dispos. 2018 Mar;46(3):237-247. doi: 10.1124/dmd.117.078899. Epub 2018 Jan 8.
Ref 231 Metabolism and Disposition of Hepatitis C Polymerase Inhibitor Dasabuvir in Humans. Drug Metab Dispos. 2016 Aug;44(8):1139-47. doi: 10.1124/dmd.115.067512. Epub 2016 May 13.
Ref 232 Characterization of human cytochrome P450 enzymes catalyzing domperidone N-dealkylation and hydroxylation in vitro. Br J Clin Pharmacol. 2004 Sep;58(3):277-87. doi: 10.1111/j.1365-2125.2004.02156.x.
Ref 233 In vitro characterization of sarizotan metabolism: hepatic clearance, identification and characterization of metabolites, drug-metabolizing enzyme identification, and evaluation of cytochrome p450 inhibition. Drug Metab Dispos. 2010 Jun;38(6):905-16. doi: 10.1124/dmd.109.029835. Epub 2010 Mar 10.
Ref 234 The prokinetic cinitapride has no clinically relevant pharmacokinetic interaction and effect on QT during coadministration with ketoconazole. Drug Metab Dispos. 2007 Jul;35(7):1149-56. doi: 10.1124/dmd.106.010835. Epub 2007 Apr 16.
Ref 235 Characterization of the metabolism of fenretinide by human liver microsomes, cytochrome P450 enzymes and UDP-glucuronosyltransferases. Br J Pharmacol. 2011 Feb;162(4):989-99. doi: 10.1111/j.1476-5381.2010.01104.x.
Ref 236 Identification of cytochrome P450 enzymes involved in the metabolism of 4'-methoxy-alpha-pyrrolidinopropiophenone (MOPPP), a designer drug, in human liver microsomes. Xenobiotica. 2003 Oct;33(10):989-98. doi: 10.1080/00498250310001602775.
Ref 237 Effects of arachidonic acid, prostaglandins, retinol, retinoic acid and cholecalciferol on xenobiotic oxidations catalysed by human cytochrome P450 enzymes. Xenobiotica. 1999 Mar;29(3):231-41. doi: 10.1080/004982599238632.
Ref 238 In vitro metabolism of rivoglitazone, a novel peroxisome proliferator-activated receptor Gamma agonist, in rat, monkey, and human liver microsomes and freshly isolated hepatocytes. Drug Metab Dispos. 2011 Jul;39(7):1311-9. doi: 10.1124/dmd.111.038729. Epub 2011 Apr 21.
Ref 239 First-in-Human Pharmacokinetic and Pharmacodynamic Study of the Dual m-TORC 1/2 Inhibitor AZD2014. Clin Cancer Res. 2015 Aug 1;21(15):3412-9. doi: 10.1158/1078-0432.CCR-14-2422. Epub 2015 Mar 24.
Ref 240 Pharmacokinetics, pharmacodynamics and safety of single, oral doses of GSK1278863, a novel HIF-prolyl hydroxylase inhibitor, in healthy Japanese and Caucasian subjects. Drug Metab Pharmacokinet. 2015 Dec;30(6):410-8. doi: 10.1016/j.dmpk.2015.08.004. Epub 2015 Aug 28.
Ref 241 Pharmacokinetics, Safety, and CCR2/CCR5 Antagonist Activity?of Cenicriviroc in Participants With Mild or Moderate Hepatic?Impairment. Clin Transl Sci. 2016 Jun;9(3):139-48. doi: 10.1111/cts.12397. Epub 2016 May 12.
Ref 242 Identification of enzymes responsible for primary and sequential oxygenation reactions of capravirine in human liver microsomes. Drug Metab Dispos. 2006 Nov;34(11):1798-802. doi: 10.1124/dmd.106.011189. Epub 2006 Aug 16.
Ref 243 Complete Substrate Inhibition of Cytochrome P450 2C8 by AZD9496, an Oral Selective Estrogen Receptor Degrader. Drug Metab Dispos. 2018 Sep;46(9):1268-1276. doi: 10.1124/dmd.118.081539. Epub 2018 Jun 19.
Ref 244 Nonclinical pharmacokinetics and in vitro metabolism of H3B-6545, a novel selective ERAlpha covalent antagonist (SERCA). Cancer Chemother Pharmacol. 2019 Jan;83(1):151-160. doi: 10.1007/s00280-018-3716-3. Epub 2018 Nov 1.
Ref 245 Steady-state pharmacokinetics of a new antipsychotic agent perospirone and its active metabolite, and its relationship with prolactin response. Ther Drug Monit. 2004 Aug;26(4):361-5. doi: 10.1097/00007691-200408000-00004.
Ref 246 Disposition and metabolism of the cathepsin K inhibitor odanacatib in humans. Drug Metab Dispos. 2014 May;42(5):818-27. doi: 10.1124/dmd.113.056580. Epub 2014 Feb 19.
Ref 247 Characterization of human cytochrome P450 enzymes involved in the metabolism of cyamemazine. Eur J Pharm Sci. 2007 Dec;32(4-5):357-66. doi: 10.1016/j.ejps.2007.09.003. Epub 2007 Sep 14.
Ref 248 Diazinon, chlorpyrifos and parathion are metabolised by multiple cytochromes P450 in human liver. Toxicology. 2006 Jul 5;224(1-2):22-32. doi: 10.1016/j.tox.2006.04.024. Epub 2006 Apr 26.
Ref 249 Identification of cytochromes P450 involved in the human liver microsomal metabolism of the thromboxane A2 inhibitor seratrodast (ABT-001). Drug Metab Dispos. 1997 Jan;25(1):110-5.
Ref 250 Exposure and response analysis of aleglitazar on cardiovascular risk markers and safety outcomes: An analysis of the AleCardio trial. Diabetes Obes Metab. 2020 Jan;22(1):30-38. doi: 10.1111/dom.13862. Epub 2019 Oct 1.
Ref 251 Mettl14 mediates the inflammatory response of macrophages in atherosclerosis through the NF-KappaB/IL-6 signaling pathway. Cell Mol Life Sci. 2022 May 22;79(6):311. doi: 10.1007/s00018-022-04331-0.
Ref 252 ClinicalTrials.gov (NCT03672305) Clinical Study on the Efficacy and Safety of c-Met/PD-L1 CAR-T Cell Injection in the Treatment of HCC
Ref 253 Clinical pipeline report, company report or official report of Catabasis Pharmaceuticals Inc.
Ref 254 N(6)-methyladenosine-dependent RNA structural switches regulate RNA-protein interactions. Nature. 2015 Feb 26;518(7540):560-4. doi: 10.1038/nature14234.
Ref 255 Leucettines, a class of potent inhibitors of cdc2-like kinases and dual specificity, tyrosine phosphorylation regulated kinases derived from the marine sponge leucettamine B: modulation of alternative pre-RNA splicing. J Med Chem. 2011 Jun 23;54(12):4172-86. doi: 10.1021/jm200274d. Epub 2011 May 26.
Ref 256 Small-molecule pyrimidine inhibitors of the cdc2-like (Clk) and dual specificity tyrosine phosphorylation-regulated (Dyrk) kinases: development of chemical probe ML315. Bioorg Med Chem Lett. 2013 Jun 15;23(12):3654-61. doi: 10.1016/j.bmcl.2013.02.096. Epub 2013 Mar 30.
Ref 257 Tricyclic Pyrimidines As Inhibitors of DYRK1A/DYRK1B As Potential Treatment for Down's Syndrome or Alzheimer's Disease. ACS Med Chem Lett. 2013 Apr 26;4(6):502-3. doi: 10.1021/ml400137s. eCollection 2013 Jun 13.
Ref 258 m(6)A RNA Methylation Regulates the Self-Renewal and Tumorigenesis of Glioblastoma Stem Cells. Cell Rep. 2017 Mar 14;18(11):2622-2634. doi: 10.1016/j.celrep.2017.02.059.
Ref 259 Structure-based optimization of potent and selective inhibitors of the tyrosine kinase erythropoietin producing human hepatocellular carcinoma receptor B4 (EphB4). J Med Chem. 2009 Oct 22;52(20):6433-46. doi: 10.1021/jm9009444.
Ref 260 US patent application no. 6,187,587, Antisense inhibition of e2f transcription factor 1 expression.
Ref 261 Dynamic m(6)A mRNA Methylation Reveals the Role of METTL3/14-m(6)A-MNK2-ERK Signaling Axis in Skeletal Muscle Differentiation and Regeneration. Front Cell Dev Biol. 2021 Oct 1;9:744171. doi: 10.3389/fcell.2021.744171. eCollection 2021.
Ref 262 National Cancer Institute Drug Dictionary (drug name SEphB4-HSA).
Ref 263 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Target id: 2109).
Ref 264 Three-dimensional structure of the EphB2 receptor in complex with an antagonistic peptide reveals a novel mode of inhibition. J Biol Chem. 2007 Dec 14;282(50):36505-13. doi: 10.1074/jbc.M706340200. Epub 2007 Sep 26.
Ref 265 METTL14 Inhibits Hepatocellular Carcinoma Metastasis Through Regulating EGFR/PI3K/AKT Signaling Pathway in an m6A-Dependent Manner. Cancer Manag Res. 2020 Dec 23;12:13173-13184. doi: 10.2147/CMAR.S286275. eCollection 2020.
Ref 266 A comparison of physicochemical property profiles of marketed oral drugs and orally bioavailable anti-cancer protein kinase inhibitors in clinical development. Curr Top Med Chem. 2007;7(14):1408-22.
Ref 267 Clinical pipeline report, company report or official report of GlaxoSmithKline (2009).
Ref 268 Rindopepimut, a 14-mer injectable peptide vaccine against EGFRvIII for the potential treatment of glioblastoma multiforme. Curr Opin Mol Ther. 2010 Dec;12(6):741-54.
Ref 269 Synthesis and Src kinase inhibitory activity of a series of 4-[(2,4-dichloro-5-methoxyphenyl)amino]-7-furyl-3-quinolinecarbonitriles. J Med Chem. 2006 Dec 28;49(26):7868-76. doi: 10.1021/jm061031t.
Ref 270 Triple negative breast cancer--current status and prospective targeted treatment based on HER1 (EGFR), TOP2A and C-MYC gene assessment. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2009 Mar;153(1):13-7. doi: 10.5507/bp.2009.002.
Ref 271 Molecular inhibition of angiogenesis and metastatic potential in human squamous cell carcinomas after epidermal growth factor receptor blockade. Mol Cancer Ther. 2002 May;1(7):507-14.
Ref 272 Integration of panitumumab into the treatment of colorectal cancer. Crit Rev Oncol Hematol. 2010 Apr;74(1):16-26. doi: 10.1016/j.critrevonc.2009.06.005. Epub 2009 Jul 17.
Ref 273 Emerging drugs for diabetic foot ulcers. Expert Opin Emerg Drugs. 2006 Nov;11(4):709-24. doi: 10.1517/14728214.11.4.709.
Ref 274 Boehringer Ingelheim. Product Development Pipeline. June 2 2009.
Ref 275 Nasopharyngeal carcinoma: Current treatment options and future directions. J Nasopharyng Carcinoma, 2014, 1(16): e16.
Ref 276 Quantitative prediction of fold resistance for inhibitors of EGFR. Biochemistry. 2009 Sep 8;48(35):8435-48. doi: 10.1021/bi900729a.
Ref 277 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Target id: 1797).
Ref 278 2017 FDA drug approvals. Nat Rev Drug Discov. 2018 Feb;17(2):81-85. doi: 10.1038/nrd.2018.4. Epub 2018 Jan 19.
Ref 279 Clinical pipeline report, company report or official report of Ionis Pharmaceuticals.
Ref 280 Phase I study of icotinib hydrochloride (BPI-2009H), an oral EGFR tyrosine kinase inhibitor, in patients with advanced NSCLC and other solid tumors. Lung Cancer. 2011 Aug;73(2):195-202. doi: 10.1016/j.lungcan.2010.11.007. Epub 2010 Dec 8.
Ref 281 AZD9291, an irreversible EGFR TKI, overcomes T790M-mediated resistance to EGFR inhibitors in lung cancer. Cancer Discov. 2014 Sep;4(9):1046-61. doi: 10.1158/2159-8290.CD-14-0337. Epub 2014 Jun 3.
Ref 282 Antitumor Activity of Amivantamab (JNJ-61186372), an EGFR-MET Bispecific Antibody, in Diverse Models of EGFR Exon 20 Insertion-Driven NSCLC. Cancer Discov. 2020 Aug;10(8):1194-1209. doi: 10.1158/2159-8290.CD-20-0116. Epub 2020 May 15.
Ref 283 Rociletinib in EGFR-mutated non-small-cell lung cancer. N Engl J Med. 2015 Apr 30;372(18):1700-9. doi: 10.1056/NEJMoa1413654.
Ref 284 Safety, Efficacy, and Pharmacokinetics of Almonertinib (HS-10296) in Pretreated Patients With EGFR-Mutated Advanced NSCLC: A Multicenter, Open-label, Phase 1 Trial. J Thorac Oncol. 2020 Dec;15(12):1907-1918. doi: 10.1016/j.jtho.2020.09.001. Epub 2020 Sep 9.
Ref 285 Dual irreversible kinase inhibitors: quinazoline-based inhibitors incorporating two independent reactive centers with each targeting different cysteine residues in the kinase domains of EGFR and VEGFR-2. Bioorg Med Chem. 2007 Jun 1;15(11):3635-48. doi: 10.1016/j.bmc.2007.03.055. Epub 2007 Mar 23.
Ref 286 ClinicalTrials.gov (NCT04305795) An Open-label Study Using ASP-1929 Photoimmunotherapy in Combination With Anti-PD1 Therapy in EGFR Expressing Advanced Solid Tumors. U.S. National Institutes of Health.
Ref 287 Pyrrolo[2,3-d]pyrimidines active as Btk inhibitors. Expert Opin Ther Pat. 2017 Dec;27(12):1305-1318. doi: 10.1080/13543776.2017.1355908. Epub 2017 Jul 20.
Ref 288 Marine-Sourced Anti-Cancer and Cancer Pain Control Agents in Clinical and Late Preclinical Development. Mar Drugs. 2014 January; 12(1): 255-278.
Ref 289 Matuzumab binding to EGFR prevents the conformational rearrangement required for dimerization. Cancer Cell. 2008 Apr;13(4):365-73. doi: 10.1016/j.ccr.2008.02.019.
Ref 290 Clinical pipeline report, company report or official report of EpimAb Biotherapeutics.
Ref 291 ClinicalTrials.gov (NCT03152435) EGFR CART Cells for Patients With Metastatic Colorectal Cancer
Ref 292 Phase I dose escalation study of ASP8273, a mutant-selective irreversible EGFR inhibitor, in subjects with EGFR mutation positive NSCLC, Journal of Clinical Oncology, Vol 33, No 15_suppl (May 20 Supplement), 2015: 8083.
Ref 293 Clinical pipeline report, company report or official report of Zentalis Pharmaceuticals.
Ref 294 ClinicalTrials.gov (NCT01869166) Treatment of Chemotherapy Refractory EGFR(Epidermal Growth Factor Receptor) Positive Advanced Solid Tumors (CART-EGFR)
Ref 295 BiPar Sciences Co-founder Reunites Management Team At TriAct Therapeutics to Advance Clinical Stage Cancer Programs. TriAct Therapeutics. Sept. 10, 2009.
Ref 296 Tarloxotinib Is a Hypoxia-Activated Pan-HER Kinase Inhibitor Active Against a Broad Range of HER-Family Oncogenes. Clin Cancer Res. 2021 Mar 1;27(5):1463-1475. doi: 10.1158/1078-0432.CCR-20-3555. Epub 2020 Dec 22.
Ref 297 Preclinical pharmacokinetics and in vitro metabolism of BMS-690514, a potent inhibitor of EGFR and VEGFR2. J Pharm Sci. 2010 Aug;99(8):3579-93. doi: 10.1002/jps.22099.
Ref 298 EGFR tyrosine kinase inhibitor pelitinib regulates radiation-induced p65-dependent telomerase activation in squamous cell carcinoma. Radiat Res. 2013 Mar;179(3):304-12. doi: 10.1667/RR3028.1. Epub 2013 Feb 4.
Ref 299 AC480, formerly BMS-599626, a pan Her inhibitor, enhances radiosensitivity and radioresponse of head and neck squamous cell carcinoma cells in vitro and in vivo. Invest New Drugs. 2011 Aug;29(4):554-61. doi: 10.1007/s10637-010-9389-3. Epub 2010 Feb 2.
Ref 300 Sym004, a novel EGFR antibody mixture, can overcome acquired resistance to cetuximab. Neoplasia. 2013 Oct;15(10):1196-206. doi: 10.1593/neo.131584.
Ref 301 Monoclonal antibodies to target epidermal growth factor receptor-positive tumors: a new paradigm for cancer therapy. Cancer. 2002 Mar 1;94(5):1593-611. doi: 10.1002/cncr.10372.
Ref 302 Clinical pipeline report, company report or official report of Black Diamond Therapeutics.
Ref 303 Characterization of ABT-806, a Humanized Tumor-Specific Anti-EGFR Monoclonal Antibody. Mol Cancer Ther. 2015 May;14(5):1141-51. doi: 10.1158/1535-7163.MCT-14-0820. Epub 2015 Mar 2.
Ref 304 Molecular mechanisms of resistance to the EGFR monoclonal antibody cetuximab. Cancer Biol Ther. 2011 May 1;11(9):777-92. doi: 10.4161/cbt.11.9.15050. Epub 2011 May 1.
Ref 305 Clinical pipeline report, company report or official report of Affimed Therapeutics.
Ref 306 AST1306, a novel irreversible inhibitor of the epidermal growth factor receptor 1 and 2, exhibits antitumor activity both in vitro and in vivo. PLoS One. 2011;6(7):e21487. doi: 10.1371/journal.pone.0021487. Epub 2011 Jul 18.
Ref 307 ClinicalTrials.gov (NCT03638167) EGFR806-specific CAR T Cell Locoregional Immunotherapy for EGFR-positive Recurrent or Refractory Pediatric CNS Tumors
Ref 308 TAS6417, A Novel EGFR Inhibitor Targeting Exon 20 Insertion Mutations. Mol Cancer Ther. 2018 Aug;17(8):1648-1658. doi: 10.1158/1535-7163.MCT-17-1206. Epub 2018 May 10.
Ref 309 Improved efficacy against malignant brain tumors with EGFRwt/EGFRvIII targeting immunotoxin and checkpoint inhibitor combinations. J Immunother Cancer. 2019 May 29;7(1):142. doi: 10.1186/s40425-019-0614-0.
Ref 310 World Antibody-Drug Conjugate Summit, October 15-16, 2013, San Francisco, CA. MAbs. 2014 January 1; 6(1): 18-29.
Ref 311 Company report (Biooncology)
Ref 312 Clinical pipeline report, company report or official report of SystImmune.
Ref 313 Bispecific antibodies rise again. Nat Rev Drug Discov. 2014 Nov;13(11):799-801. doi: 10.1038/nrd4478.
Ref 314 Clinical pipeline report, company report or official report of Merus.
Ref 315 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
Ref 316 ClinicalTrials.gov (NCT02331693) CAR T Cells in Treating Patients With Malignant Gliomas Overexpressing EGFR
Ref 317 National Cancer Institute Drug Dictionary (drug id 596693).
Ref 318 Clinical pipeline report, company report or official report of Shionogi (2011).
Ref 319 AMG 595, an Anti-EGFRvIII Antibody-Drug Conjugate, Induces Potent Antitumor Activity against EGFRvIII-Expressing Glioblastoma. Mol Cancer Ther. 2015 Jul;14(7):1614-24. doi: 10.1158/1535-7163.MCT-14-1078. Epub 2015 Apr 30.
Ref 320 Antitumor Effects of EGFR Antisense Guanidine-Based Peptide Nucleic Acids in Cancer Models. ACS Chem Biol. 2013 February 15; 8(2): 345-352.
Ref 321 ClinicalTrials.gov (NCT04429542) Study of Safety and Tolerability of BCA101 Alone and in Combination With Pembrolizumab in Patients With EGFR-driven Advanced Solid Tumors. U.S. National Institutes of Health.
Ref 322 Clinical pipeline report, company report or official report of Bristol-Myers Squibb.
Ref 323 Protein-tyrosine kinase inhibition: mechanism-based discovery of antitumor agents. J Nat Prod. 1992 Nov;55(11):1529-60. doi: 10.1021/np50089a001.
Ref 324 Tyrosine kinase inhibitors. 9. Synthesis and evaluation of fused tricyclic quinazoline analogues as ATP site inhibitors of the tyrosine kinase activity of the epidermal growth factor receptor. J Med Chem. 1996 Feb 16;39(4):918-28. doi: 10.1021/jm950692f.
Ref 325 Biochemical and cellular effects of c-Src kinase-selective pyrido[2, 3-d]pyrimidine tyrosine kinase inhibitors. Biochem Pharmacol. 2000 Oct 1;60(7):885-98. doi: 10.1016/s0006-2952(00)00405-6.
Ref 326 Tyrphostins. 2. Heterocyclic and alpha-substituted benzylidenemalononitrile tyrphostins as potent inhibitors of EGF receptor and ErbB2/neu tyrosine kinases. J Med Chem. 1991 Jun;34(6):1896-907. doi: 10.1021/jm00110a022.
Ref 327 5,7-Dimethoxy-3-(4-pyridinyl)quinoline is a potent and selective inhibitor of human vascular beta-type platelet-derived growth factor receptor tyrosine kinase. J Med Chem. 1994 Aug 19;37(17):2627-9. doi: 10.1021/jm00043a002.
Ref 328 Design, synthesis, and biological evaluation of 3,4-diarylmaleimides as angiogenesis inhibitors. J Med Chem. 2006 Feb 23;49(4):1271-81. doi: 10.1021/jm0580297.
Ref 329 5-Benzylidene-hydantoins: synthesis and antiproliferative activity on A549 lung cancer cell line. Eur J Med Chem. 2009 Sep;44(9):3471-9. doi: 10.1016/j.ejmech.2009.01.035. Epub 2009 Feb 7.
Ref 330 Optimization of 6,7-disubstituted-4-(arylamino)quinoline-3-carbonitriles as orally active, irreversible inhibitors of human epidermal growth factor receptor-2 kinase activity. J Med Chem. 2005 Feb 24;48(4):1107-31. doi: 10.1021/jm040159c.
Ref 331 Computational studies of epidermal growth factor receptor: docking reliability, three-dimensional quantitative structure-activity relationship analysis, and virtual screening studies. J Med Chem. 2009 Feb 26;52(4):964-75. doi: 10.1021/jm800829v.
Ref 332 Biological evaluation of a multi-targeted small molecule inhibitor of tumor-induced angiogenesis. Bioorg Med Chem Lett. 2006 Apr 1;16(7):1950-3. doi: 10.1016/j.bmcl.2005.12.092. Epub 2006 Feb 3.
Ref 333 Novel antiproliferative agents derived from lavendustin A. J Med Chem. 1994 Nov 25;37(24):4079-84. doi: 10.1021/jm00050a005.
Ref 334 Discovery and SAR of 6-substituted-4-anilinoquinazolines as non-competitive antagonists of mGlu5. Bioorg Med Chem Lett. 2009 Dec 1;19(23):6623-6. doi: 10.1016/j.bmcl.2009.10.024. Epub 2009 Oct 9.
Ref 335 A novel series of 4-phenoxyquinolines: potent and highly selective inhibitors of PDGF receptor autophosphorylation, Bioorg. Med. Chem. Lett. 7(23):2935-2940 (1997).
Ref 336 Structure-guided development of affinity probes for tyrosine kinases using chemical genetics. Nat Chem Biol. 2007 Apr;3(4):229-38. doi: 10.1038/nchembio866. Epub 2007 Mar 4.
Ref 337 Acryloylamino-salicylanilides as EGFR PTK inhibitors. Bioorg Med Chem Lett. 2006 Jan 15;16(2):469-72. doi: 10.1016/j.bmcl.2005.06.088. Epub 2005 Nov 3.
Ref 338 Synthesis and inhibitory activity of 4-alkynyl and 4-alkenylquinazolines: identification of new scaffolds for potent EGFR tyrosine kinase inhibitors. Bioorg Med Chem Lett. 2007 Nov 1;17(21):5863-7. doi: 10.1016/j.bmcl.2007.08.020. Epub 2007 Aug 15.
Ref 339 Tyrosine kinase inhibitors. 19. 6-Alkynamides of 4-anilinoquinazolines and 4-anilinopyrido[3,4-d]pyrimidines as irreversible inhibitors of the erbB family of tyrosine kinase receptors. J Med Chem. 2006 Feb 23;49(4):1475-85. doi: 10.1021/jm050936o.
Ref 340 Selected novel anticancer treatments targeting cell signaling proteins. Oncologist. 2001;6(6):517-37. doi: 10.1634/theoncologist.6-6-517.
Ref 341 The combi-targeting concept: synthesis of stable nitrosoureas designed to inhibit the epidermal growth factor receptor (EGFR). J Med Chem. 2006 Jun 15;49(12):3544-52. doi: 10.1021/jm0600390.
Ref 342 A systematic interaction map of validated kinase inhibitors with Ser/Thr kinases. Proc Natl Acad Sci U S A. 2007 Dec 18;104(51):20523-8. doi: 10.1073/pnas.0708800104. Epub 2007 Dec 11.
Ref 343 Tyrphostins I: synthesis and biological activity of protein tyrosine kinase inhibitors. J Med Chem. 1989 Oct;32(10):2344-52. doi: 10.1021/jm00130a020.
Ref 344 Tyrosine kinase inhibitors. 5. Synthesis and structure-activity relationships for 4-[(phenylmethyl)amino]- and 4-(phenylamino)quinazolines as potent adenosine 5'-triphosphate binding site inhibitors of the tyrosine kinase domain of the epidermal growth factor receptor. J Med Chem. 1995 Sep 1;38(18):3482-7. doi: 10.1021/jm00018a008.
Ref 345 Synthesis of a prodrug designed to release multiple inhibitors of the epidermal growth factor receptor tyrosine kinase and an alkylating agent: a novel tumor targeting concept. J Med Chem. 2003 Dec 4;46(25):5546-51. doi: 10.1021/jm030423m.
Ref 346 Discovery of a series of 2,5-diaminopyrimidine covalent irreversible inhibitors of Bruton's tyrosine kinase with in vivo antitumor activity. J Med Chem. 2014 Jun 26;57(12):5112-28. doi: 10.1021/jm4017762. Epub 2014 Jun 10.
Ref 347 Anthraquinones and betaenone derivatives from the sponge-associated fungus Microsphaeropsis species: novel inhibitors of protein kinases. J Nat Prod. 2000 Jun;63(6):739-45. doi: 10.1021/np9905259.
Ref 348 Indazolylamino quinazolines and pyridopyrimidines as inhibitors of the EGFr and C-erbB-2. Bioorg Med Chem Lett. 2001 Jun 4;11(11):1401-5. doi: 10.1016/s0960-894x(01)00219-0.
Ref 349 Targeted polypharmacology: discovery of dual inhibitors of tyrosine and phosphoinositide kinases. Nat Chem Biol. 2008 Nov;4(11):691-9. doi: 10.1038/nchembio.117. Epub 2008 Oct 12.
Ref 350 Cochliobolic acid, a novel metabolite produced by Cochliobolus lunatus, inhibits binding of TGF-alpha to the EGF receptor in a SPA assay. J Nat Prod. 1997 Jan;60(1):6-8. doi: 10.1021/np9605293.
Ref 351 Syntheses of 4-(indole-3-yl)quinazolines: a new class of epidermal growth factor receptor tyrosine kinase inhibitors. Eur J Med Chem. 2008 Jul;43(7):1478-88. doi: 10.1016/j.ejmech.2007.09.018. Epub 2007 Sep 29.
Ref 352 Use of a pharmacophore model for the design of EGFR tyrosine kinase inhibitors: isoflavones and 3-phenyl-4(1H)-quinolones. J Med Chem. 1999 Mar 25;42(6):1018-26. doi: 10.1021/jm980551o.
Ref 353 Retinoic acid-induced RB (retinoblastoma) hypophosphorylation enhanced by CGP 52411 (4,5-dianilinophthalimide), an EGF family tyrosine kinase receptor inhibitor. Eur J Cell Biol. 1996 Apr;69(4):327-34.
Ref 354 Tyrosine kinase inhibitors. 10. Isomeric 4-[(3-bromophenyl)amino]pyrido[d]-pyrimidines are potent ATP binding site inhibitors of the tyrosine kinase function of the epidermal growth factor receptor. J Med Chem. 1996 Apr 26;39(9):1823-35. doi: 10.1021/jm9508651.
Ref 355 Novel nitrogen mustard-armed combi-molecules for the selective targeting of epidermal growth factor receptor overexperessing solid tumors: discovery of an unusual structure-activity relationship. J Med Chem. 2007 May 31;50(11):2605-8. doi: 10.1021/jm070144p. Epub 2007 May 2.
Ref 356 Tyrosine kinase inhibitors. 15. 4-(Phenylamino)quinazoline and 4-(phenylamino)pyrido[d]pyrimidine acrylamides as irreversible inhibitors of the ATP binding site of the epidermal growth factor receptor. J Med Chem. 1999 May 20;42(10):1803-15. doi: 10.1021/jm9806603.
Ref 357 Growth factors and their receptors: new targets for prostate cancer therapy. Urology. 2001 Aug;58(2 Suppl 1):114-22. doi: 10.1016/s0090-4295(01)01253-5.
Ref 358 Effects of hEGF (MG111) on gastric mucosal potential difference in rats. Scand J Gastroenterol Suppl. 1989;162:198-201. doi: 10.3109/00365528909091160.
Ref 359 Tyrosine kinase inhibitors. 8. An unusually steep structure-activity relationship for analogues of 4-(3-bromoanilino)-6,7-dimethoxyquinazoline (PD 153035), a potent inhibitor of the epidermal growth factor receptor. J Med Chem. 1996 Jan 5;39(1):267-76. doi: 10.1021/jm9503613.
Ref 360 The specificity of JAK3 kinase inhibitors. Blood. 2008 Feb 15;111(4):2155-7. doi: 10.1182/blood-2007-09-115030. Epub 2007 Dec 19.
Ref 361 The heparin-binding domain of heparin-binding EGF-like growth factor can target Pseudomonas exotoxin to kill cells exclusively through heparan sulfate proteoglycans. J Cell Sci. 1994 Sep;107 ( Pt 9):2599-608. doi: 10.1242/jcs.107.9.2599.
Ref 362 WO patent application no. 2009,0582,67, Benzomorpholine derivatives and methods of use.
Ref 363 A comparison of EGF and MAb 528 labeled with 111In for imaging human breast cancer. J Nucl Med. 2000 May;41(5):903-11.
Ref 364 GA201 (RG7160): a novel, humanized, glycoengineered anti-EGFR antibody with enhanced ADCC and superior in vivo efficacy compared with cetuximab. Clin Cancer Res. 2013 Mar 1;19(5):1126-38. doi: 10.1158/1078-0432.CCR-12-0989. Epub 2012 Dec 3.
Ref 365 Phase I and pharmacokinetic study of BIBX 1382 BS, an epidermal growth factor receptor (EGFR) inhibitor, given in a continuous daily oral administration. Eur J Cancer. 2002 May;38(8):1072-80. doi: 10.1016/s0959-8049(02)00020-5.
Ref 366 Epidermal growth factor receptor inhibitor PKI-166 governs cardiovascular protection without beneficial effects on the kidney in hypertensive 5/6 nephrectomized rats. J Pharmacol Exp Ther. 2013 Jun;345(3):393-403. doi: 10.1124/jpet.113.203497. Epub 2013 Mar 25.
Ref 367 EGFR tyrosine kinase inhibitor (PD153035) improves glucose tolerance and insulin action in high-fat diet-fed mice. Diabetes. 2009 Dec;58(12):2910-9. doi: 10.2337/db08-0506. Epub 2009 Aug 20.
Ref 368 Recognition of RNA N(6)-methyladenosine by IGF2BP proteins enhances mRNA stability and translation. Nat Cell Biol. 2018 Mar;20(3):285-295. doi: 10.1038/s41556-018-0045-z. Epub 2018 Feb 23.
Ref 369 Specificity and mechanism of action of some commonly used protein kinase inhibitors. Biochem J. 2000 Oct 1;351(Pt 1):95-105. doi: 10.1042/0264-6021:3510095.
Ref 370 US patent application no. 6,187,586, Antisense modulation of AKT-3 expression.
Ref 371 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Target id: 1811).
Ref 372 Pyrido[2,3-d]pyrimidin-7-one inhibitors of cyclin-dependent kinases. J Med Chem. 2000 Nov 30;43(24):4606-16. doi: 10.1021/jm000271k.
Ref 373 METTL14 aggravates endothelial inflammation and atherosclerosis by increasing FOXO1 N6-methyladeosine modifications. Theranostics. 2020 Jul 11;10(20):8939-8956. doi: 10.7150/thno.45178. eCollection 2020.
Ref 374 (R)-PFI-2 is a potent and selective inhibitor of SETD7 methyltransferase activity in cells. Proc Natl Acad Sci U S A. 2014 Sep 2;111(35):12853-8. doi: 10.1073/pnas.1407358111. Epub 2014 Aug 18.
Ref 375 US patent application no. 7,229,976, Modulation of forkhead box O1A expression.
Ref 376 Discovery of a (1H-benzoimidazol-2-yl)-1H-pyridin-2-one (BMS-536924) inhibitor of insulin-like growth factor I receptor kinase with in vivo antitumor activity. J Med Chem. 2005 Sep 8;48(18):5639-43. doi: 10.1021/jm050392q.
Ref 377 Discovery of potent and bioavailable GSK-3beta inhibitors. Bioorg Med Chem Lett. 2010 Mar 1;20(5):1693-6. doi: 10.1016/j.bmcl.2010.01.038. Epub 2010 Jan 25.
Ref 378 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Target id: 2030).
Ref 379 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
Ref 380 The GSK3 kinase inhibitor lithium produces unexpected hyperphosphorylation of Beta-catenin, a GSK3 substrate, in human glioblastoma cells. Biol Open. 2018 Jan 26;7(1):bio030874. doi: 10.1242/bio.030874.
Ref 381 Evidence for irreversible inhibition of glycogen synthase kinase-3Beta by tideglusib. J Biol Chem. 2012 Jan 6;287(2):893-904. doi: 10.1074/jbc.M111.306472. Epub 2011 Nov 18.
Ref 382 Glycogen synthase kinase 3 (GSK-3) inhibitors: a patent update (2014-2015). Expert Opin Ther Pat. 2017 Jun;27(6):657-666. doi: 10.1080/13543776.2017.1259412. Epub 2016 Nov 21.
Ref 383 Design of potent and selective GSK3beta inhibitors with acceptable safety profile and pharmacokinetics. Bioorg Med Chem Lett. 2010 Apr 1;20(7):2344-9. doi: 10.1016/j.bmcl.2010.01.132. Epub 2010 Feb 2.
Ref 384 Glycogen synthase kinase-3 (GSK-3) inhibitory activity and structure-activity relationship (SAR) studies of the manzamine alkaloids. Potential for Alzheimer's disease. J Nat Prod. 2007 Sep;70(9):1397-405. doi: 10.1021/np060092r. Epub 2007 Aug 21.
Ref 385 Novel 8-arylated purines as inhibitors of glycogen synthase kinase. Eur J Med Chem. 2010 Aug;45(8):3389-93. doi: 10.1016/j.ejmech.2010.04.026. Epub 2010 Apr 28.
Ref 386 Optimization of protein kinase CK2 inhibitors derived from 4,5,6,7-tetrabromobenzimidazole. J Med Chem. 2004 Dec 2;47(25):6239-47. doi: 10.1021/jm049854a.
Ref 387 The identification of potent and selective imidazole-based inhibitors of B-Raf kinase. Bioorg Med Chem Lett. 2006 Jan 15;16(2):378-81. doi: 10.1016/j.bmcl.2005.09.072. Epub 2005 Nov 2.
Ref 388 Manzamine B and E and ircinal A related alkaloids from an Indonesian Acanthostrongylophora sponge and their activity against infectious, tropical parasitic, and Alzheimer's diseases. J Nat Prod. 2006 Jul;69(7):1034-40. doi: 10.1021/np0601399.
Ref 389 The selectivity of protein kinase inhibitors: a further update. Biochem J. 2007 Dec 15;408(3):297-315. doi: 10.1042/BJ20070797.
Ref 390 Novel small molecule inhibitors of 3-phosphoinositide-dependent kinase-1. J Biol Chem. 2005 May 20;280(20):19867-74. doi: 10.1074/jbc.M501367200. Epub 2005 Mar 16.
Ref 391 N-Phenyl-4-pyrazolo[1,5-b]pyridazin-3-ylpyrimidin-2-amines as potent and selective inhibitors of glycogen synthase kinase 3 with good cellular efficacy. J Med Chem. 2004 Sep 9;47(19):4716-30. doi: 10.1021/jm040063i.
Ref 392 Novel GSK-3beta inhibitors from sequential virtual screening. Bioorg Med Chem. 2008 Jan 15;16(2):636-43. doi: 10.1016/j.bmc.2007.10.047. Epub 2007 Oct 22.
Ref 393 1-Azakenpaullone is a selective inhibitor of glycogen synthase kinase-3 beta. Bioorg Med Chem Lett. 2004 Jan 19;14(2):413-6. doi: 10.1016/j.bmcl.2003.10.062.
Ref 394 How many drug targets are there Nat Rev Drug Discov. 2006 Dec;5(12):993-6.
Ref 395 Rational design of potent GSK3beta inhibitors with selectivity for Cdk1 and Cdk2. Bioorg Med Chem Lett. 2010 Mar 15;20(6):1985-9. doi: 10.1016/j.bmcl.2010.01.114. Epub 2010 Jan 25.
Ref 396 9-ING-41, a small molecule inhibitor of GSK-3beta, potentiates the effects of anticancer therapeutics in bladder cancer. Sci Rep. 2019 Dec 27;9(1):19977. doi: 10.1038/s41598-019-56461-4.
Ref 397 Novel indolylmaleimide acts as GSK-3beta inhibitor in human neural progenitor cells. Bioorg Med Chem. 2010 Sep 15;18(18):6785-95. doi: 10.1016/j.bmc.2010.07.045. Epub 2010 Jul 25.
Ref 398 Synthesis and preliminary biological evaluation of new derivatives of the marine alkaloid leucettamine B as kinase inhibitors. Eur J Med Chem. 2010 Feb;45(2):805-10. doi: 10.1016/j.ejmech.2009.10.009. Epub 2009 Oct 12.
Ref 399 Design, synthesis, and biological evaluation of novel 7-azaindolyl-heteroaryl-maleimides as potent and selective glycogen synthase kinase-3beta (GSK-3beta) inhibitors. Bioorg Med Chem. 2004 Jun 15;12(12):3167-85. doi: 10.1016/j.bmc.2004.04.010.
Ref 400 First Cdc7 kinase inhibitors: pyrrolopyridinones as potent and orally active antitumor agents. 2. Lead discovery. J Med Chem. 2009 Jan 22;52(2):293-307. doi: 10.1021/jm800977q.
Ref 401 Structural basis for the synthesis of indirubins as potent and selective inhibitors of glycogen synthase kinase-3 and cyclin-dependent kinases. J Med Chem. 2004 Feb 12;47(4):935-46. doi: 10.1021/jm031016d.
Ref 402 The discovery of the potent aurora inhibitor MK-0457 (VX-680). Bioorg Med Chem Lett. 2009 Jul 1;19(13):3586-92. doi: 10.1016/j.bmcl.2009.04.136. Epub 2009 May 3.
Ref 403 Scaffold hopping and optimization towards libraries of glycogen synthase kinase-3 inhibitors. Bioorg Med Chem Lett. 2002 Jun 3;12(11):1525-8. doi: 10.1016/s0960-894x(02)00169-5.
Ref 404 Triazolo[1,5-a]pyrimidines as novel CDK2 inhibitors: protein structure-guided design and SAR. Bioorg Med Chem Lett. 2006 Mar 1;16(5):1353-7. doi: 10.1016/j.bmcl.2005.11.048. Epub 2005 Dec 1.
Ref 405 Fragment and knowledge-based design of selective GSK-3beta inhibitors using virtual screening models. Eur J Med Chem. 2009 Jun;44(6):2361-71. doi: 10.1016/j.ejmech.2008.08.012. Epub 2008 Sep 16.
Ref 406 Synthesis and antiproliferative activity of 7-azaindirubin-3'-oxime, a 7-aza isostere of the natural indirubin pharmacophore. J Nat Prod. 2009 Dec;72(12):2199-202. doi: 10.1021/np9003905.
Ref 407 Cellular characterization of a novel focal adhesion kinase inhibitor. J Biol Chem. 2007 May 18;282(20):14845-52. doi: 10.1074/jbc.M606695200. Epub 2007 Mar 28.
Ref 408 4-arylazo-3,5-diamino-1H-pyrazole CDK inhibitors: SAR study, crystal structure in complex with CDK2, selectivity, and cellular effects. J Med Chem. 2006 Nov 2;49(22):6500-9. doi: 10.1021/jm0605740.
Ref 409 Selective glycogen synthase kinase 3 inhibitors potentiate insulin activation of glucose transport and utilization in vitro and in vivo. Diabetes. 2003 Mar;52(3):588-95. doi: 10.2337/diabetes.52.3.588.
Ref 410 Identification of ellagic acid as potent inhibitor of protein kinase CK2: a successful example of a virtual screening application. J Med Chem. 2006 Apr 20;49(8):2363-6. doi: 10.1021/jm060112m.
Ref 411 Diversity-oriented synthesis: exploring the intersections between chemistry and biology. Nat Chem Biol. 2005 Jul;1(2):74-84. doi: 10.1038/nchembio0705-74.
Ref 412 2-N-Methyl modifications and SAR studies of manzamine A. Bioorg Med Chem. 2008 Jul 15;16(14):6702-6. doi: 10.1016/j.bmc.2008.05.079. Epub 2008 Jun 5.
Ref 413 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800029796)
Ref 414 Identification of novel scaffold of benzothiazepinones as non-ATP competitive glycogen synthase kinase-3Beta inhibitors through virtual screening. Bioorg Med Chem Lett. 2012 Dec 1;22(23):7232-6. doi: 10.1016/j.bmcl.2012.09.043. Epub 2012 Sep 23.
Ref 415 Cyclin-dependent kinase inhibitors for cancer therapy: a patent review (2009 - 2014). Expert Opin Ther Pat. 2015;25(9):953-70. doi: 10.1517/13543776.2015.1045414. Epub 2015 Jul 13.
Ref 416 AZD1080, a novel GSK3 inhibitor, rescues synaptic plasticity deficits in rodent brain and exhibits peripheral target engagement in humans. J Neurochem. 2013 May;125(3):446-56. doi: 10.1111/jnc.12203. Epub 2013 Mar 11.
Ref 417 Cap-independent mRNA translation is upregulated in long-lived endocrine mutant mice. J Mol Endocrinol. 2019 Aug 1;63(2):123-138. doi: 10.1530/JME-19-0021.
Ref 418 Terameprocol, a novel site-specific transcription inhibitor with anticancer activity. IDrugs. 2008 Mar;11(3):204-14.
Ref 419 Pharmacodynamic and antineoplastic activity of BI 836845, a fully human IGF ligand-neutralizing antibody, and mechanistic rationale for combination with rapamycin. Mol Cancer Ther. 2014 Feb;13(2):399-409. doi: 10.1158/1535-7163.MCT-13-0598. Epub 2013 Dec 2.
Ref 420 RNA m(6) A modification enzymes shape innate responses to DNA by regulating interferon Beta. Genes Dev. 2018 Dec 1;32(23-24):1472-1484. doi: 10.1101/gad.319475.118. Epub 2018 Nov 21.
Ref 421 Selective inhibition of matrix metalloproteinase isozymes and in vivo protection against emphysema by substituted gamma-keto carboxylic acids. J Med Chem. 2006 Jan 26;49(2):456-8. doi: 10.1021/jm051101g.
Ref 422 2014 FDA drug approvals. Nat Rev Drug Discov. 2015 Feb;14(2):77-81. doi: 10.1038/nrd4545.
Ref 423 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services.
Ref 424 The effect of intravenous interferon-beta-1a (FP-1201) on lung CD73 expression and on acute respiratory distress syndrome mortality: an open-label study. Lancet Respir Med. 2014 Feb;2(2):98-107. doi: 10.1016/S2213-2600(13)70259-5. Epub 2013 Dec 23.
Ref 425 Pegylated interferon Beta-1a for relapsing-remitting multiple sclerosis (ADVANCE): a randomised, phase 3, double-blind study. Lancet Neurol. 2014 Jul;13(7):657-65. doi: 10.1016/S1474-4422(14)70068-7. Epub 2014 Apr 30.
Ref 426 Improving compliance with interferon-beta therapy in patients with multiple sclerosis. CNS Drugs. 2009;23(6):453-62. doi: 10.2165/00023210-200923060-00001.
Ref 427 PEGylated interferon beta-1a in the treatment of multiple sclerosis - an update. Biologics. 2013; 7: 131-138.
Ref 428 Interferon-beta gene therapy for cancer: basic research to clinical application. Cancer Sci. 2004 Nov;95(11):858-65. doi: 10.1111/j.1349-7006.2004.tb02194.x.
Ref 429 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800032947)
Ref 430 A Potent and Selective Quinoxalinone-Based STK33 Inhibitor Does Not Show Synthetic Lethality in KRAS-Dependent Cells. ACS Med Chem Lett. 2012 Dec 13;3(12):1034-1038. doi: 10.1021/ml300246r. Epub 2012 Oct 22.
Ref 431 2018 FDA drug approvals. Nat Rev Drug Discov. 2019 Feb;18(2):85-89. doi: 10.1038/d41573-019-00014-x.
Ref 432 Emerging oral drugs for multiple sclerosis. Expert Opin Emerg Drugs. 2008 Sep;13(3):465-77. doi: 10.1517/14728214.13.3.465.
Ref 433 Pharmacokinetic and pharmacodynamic characterization of a new formulation containing synergistic proportions of interferons alpha-2b and gamma (HeberPAG) in patients with mycosis fungoides: an open-label trial. BMC Pharmacol Toxicol. 2012 Dec 28;13:20. doi: 10.1186/2050-6511-13-20.
Ref 434 EP patent application no. 17782511, Nucleoside phosphonate conjugates as anti hiv agents.
Ref 435 CombinatoRx Drug Candidate CRx-191 Demonstrates Positive Phase 2 Results In Psoriasis. CombinatoRx. 2008.
Ref 436 Emerging drugs to treat Crohn's disease. Expert Opin Emerg Drugs. 2007 Mar;12(1):49-59. doi: 10.1517/14728214.12.1.49.
Ref 437 Drug evaluation: TG-1042, an adenovirus-mediated IFNgamma gene delivery for the intratumoral therapy of primary cutaneous lymphomas. Curr Opin Investig Drugs. 2007 Jun;8(6):493-8.
Ref 438 Pharmacokinetic and pharmacodynamic relationship of AMG 811, an anti-IFN-Gamma IgG1 monoclonal antibody, in patients with systemic lupus erythematosus. Pharm Res. 2015 Feb;32(2):640-53. doi: 10.1007/s11095-014-1492-2. Epub 2014 Sep 12.
Ref 439 T helper 1 inhibitor TAK-603 inhibits IFN-gamma and IL-12 production with no effect on IL-18: an observation in sarcoidosis patients. Sarcoidosis Vasc Diffuse Lung Dis. 2004 Oct;21(3):204-11.
Ref 440 Leadership in BioBusiness. Dr Gurinder S Shahi. Page(36).
Ref 441 Can we use interleukin-6 (IL-6) blockade for coronavirus disease 2019 (COVID-19)-induced cytokine release syndrome (CRS)?. J Autoimmun. 2020 Jul;111:102452. doi: 10.1016/j.jaut.2020.102452. Epub 2020 Apr 10.
Ref 442 Sirukumab: A Potential Treatment for Mood Disorders?. Adv Ther. 2017 Jan;34(1):78-90. doi: 10.1007/s12325-016-0455-x. Epub 2016 Dec 2.
Ref 443 Coronaviruses - drug discovery and therapeutic options. Nat Rev Drug Discov. 2016 May;15(5):327-47. doi: 10.1038/nrd.2015.37. Epub 2016 Feb 12.
Ref 444 Efficacy and safety of olokizumab in patients with rheumatoid arthritis with an inadequate response to TNF inhibitor therapy: outcomes of a randomised Phase IIb study. Ann Rheum Dis. 2014 September; 73(9): 1607-1615.
Ref 445 Discovery and characterization of olokizumab: a humanized antibody targeting interleukin-6 and neutralizing gp130-signaling. MAbs. 2014 May-Jun;6(3):774-82. doi: 10.4161/mabs.28612. Epub 2014 Apr 2.
Ref 446 Whole-molecule antibody engineering: generation of a high-affinity anti-IL-6 antibody with extended pharmacokinetics. J Mol Biol. 2011 Aug 26;411(4):791-807. doi: 10.1016/j.jmb.2011.06.031. Epub 2011 Jun 23.
Ref 447 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800020380)
Ref 448 A high-affinity fully human anti-IL-6 mAb (OP-R003-1, 1339) for the treatment of Multiple Myeloma
Ref 449 Methyl CpG binding protein 2 promotes colorectal cancer metastasis by regulating N(6) -methyladenosine methylation through methyltransferase-like 14. Cancer Sci. 2021 Aug;112(8):3243-3254. doi: 10.1111/cas.15011. Epub 2021 Jun 29.
Ref 450 mTORC1-chaperonin CCT signaling regulates m(6)A RNA methylation to suppress autophagy. Proc Natl Acad Sci U S A. 2021 Mar 9;118(10):e2021945118. doi: 10.1073/pnas.2021945118.
Ref 451 PPARGamma ligands and their therapeutic applications: a patent review (2008 - 2014). Expert Opin Ther Pat. 2015 Feb;25(2):175-91. doi: 10.1517/13543776.2014.985206. Epub 2014 Nov 21.
Ref 452 Constrained peptides' time to shine?. Nat Rev Drug Discov. 2018 Jul 30;17(8):531-533. doi: 10.1038/nrd.2018.125.
Ref 453 Dual mTORC1 and mTORC2 inhibitor Palomid 529 penetrates the blood-brain barrier without restriction by ABCB1 and ABCG2. Int J Cancer. 2013 Sep 1;133(5):1222-33. doi: 10.1002/ijc.28126. Epub 2013 Apr 1.
Ref 454 Sestrin modulator NV-5138 produces rapid antidepressant effects via direct mTORC1 activation. J Clin Invest. 2019 Apr 16;129(6):2542-2554. doi: 10.1172/JCI126859.
Ref 455 Stimulator of IFN genes mediates neuroinflammatory injury by suppressing AMPK signal in experimental subarachnoid hemorrhage. J Neuroinflammation. 2020 May 25;17(1):165. doi: 10.1186/s12974-020-01830-4.
Ref 456 Decrease of cyclin D1 in the human lung adenocarcinoma cell line A-427 by 7-hydroxycoumarin. Lung Cancer. 2001 Nov;34(2):185-94. doi: 10.1016/s0169-5002(01)00263-x.
Ref 457 METTL14 aggravates podocyte injury and glomerulopathy progression through N(6)-methyladenosine-dependent downregulating of Sirt1. Cell Death Dis. 2021 Sep 27;12(10):881. doi: 10.1038/s41419-021-04156-y.
Ref 458 Pharmacological activation of Sirt1 ameliorates polyglutamine-induced toxicity through the regulation of autophagy. PLoS One. 2013 Jun 10;8(6):e64953. doi: 10.1371/journal.pone.0064953. Print 2013.
Ref 459 Sirtuin modulators: an updated patent review (2012 - 2014).Expert Opin Ther Pat. 2015 Jan;25(1):5-15.
Ref 460 Sirtuin 1 activator SRT2104 protects Huntington's disease mice. Ann Clin Transl Neurol. 2014 Dec;1(12):1047-52. doi: 10.1002/acn3.135. Epub 2014 Oct 31.
Ref 461 The Sirt1 Activators SRT2183 and SRT3025 Inhibit RANKL-Induced Osteoclastogenesis in Bone Marrow-Derived Macrophages and Down-Regulate Sirt3 in Sirt1 Null Cells. PLoS One. 2015 Jul 30;10(7):e0134391. doi: 10.1371/journal.pone.0134391. eCollection 2015.
Ref 462 Sirtuin 1 (SIRT1): the misunderstood HDAC. J Biomol Screen. 2011 Dec;16(10):1153-69. doi: 10.1177/1087057111422103. Epub 2011 Nov 15.
Ref 463 Design, synthesis, and biological evaluation of sirtinol analogues as class III histone/protein deacetylase (Sirtuin) inhibitors. J Med Chem. 2005 Dec 1;48(24):7789-95. doi: 10.1021/jm050100l.
Ref 464 Adenosine mimetics as inhibitors of NAD+-dependent histone deacetylases, from kinase to sirtuin inhibition. J Med Chem. 2006 Dec 14;49(25):7307-16. doi: 10.1021/jm060118b.
Ref 465 Discovery of indoles as potent and selective inhibitors of the deacetylase SIRT1. J Med Chem. 2005 Dec 15;48(25):8045-54. doi: 10.1021/jm050522v.
Ref 466 Characterization of sirtuin inhibitors in nematodes expressing a muscular dystrophy protein reveals muscle cell and behavioral protection by specific sirtinol analogues. J Med Chem. 2010 Feb 11;53(3):1407-11. doi: 10.1021/jm9013345.
Ref 467 Small molecule activators of SIRT1 as therapeutics for the treatment of type 2 diabetes. Nature. 2007 Nov 29;450(7170):712-6. doi: 10.1038/nature06261.
Ref 468 SRT2379, a small-molecule SIRT1 activator, fails to reduce cytokine release in a human endotoxemia model. Critical Care 2013, 17(Suppl 4):P8.
Ref 469 m(6)A mRNA modification maintains colonic epithelial cell homeostasis via NF-KappaB-mediated antiapoptotic pathway. Sci Adv. 2022 Mar 25;8(12):eabl5723. doi: 10.1126/sciadv.abl5723. Epub 2022 Mar 25.
Ref 470 US patent application no. 7,217,572, Modulation of HIF1.alpha. and HIF2.alpha. expression.
Ref 471 Protective effect of Indole-3-carbinol, an NF-KappaB inhibitor in experimental paradigm of Parkinson's disease: In silico and in vivo studies. Brain Behav Immun. 2020 Nov;90:108-137. doi: 10.1016/j.bbi.2020.08.001. Epub 2020 Aug 12.
Ref 472 Mettl14 inhibits bladder TIC self-renewal and bladder tumorigenesis through N(6)-methyladenosine of Notch1. Mol Cancer. 2019 Nov 25;18(1):168. doi: 10.1186/s12943-019-1084-1.
Ref 473 EIAV-based retinal gene therapy in the shaker1 mouse model for usher syndrome type 1B: development of UshStat. PLoS One. 2014 Apr 4;9(4):e94272. doi: 10.1371/journal.pone.0094272. eCollection 2014.
Ref 474 A METTL3-METTL14 complex mediates mammalian nuclear RNA N6-adenosine methylation. Nat Chem Biol. 2014 Feb;10(2):93-5. doi: 10.1038/nchembio.1432. Epub 2013 Dec 6.
Ref 475 Peroxisome proliferator-activated receptor alpha activators improve insulin sensitivity and reduce adiposity. J Biol Chem. 2000 Jun 2;275(22):16638-42. doi: 10.1074/jbc.275.22.16638.
Ref 476 Muraglitazar, a dual (alpha/gamma) PPAR activator: a randomized, double-blind, placebo-controlled, 24-week monotherapy trial in adult patients with type 2 diabetes. Clin Ther. 2005 Aug;27(8):1181-95. doi: 10.1016/j.clinthera.2005.08.005.
Ref 477 Bezafibrate at clinically relevant doses decreases serum/liver triglycerides via down-regulation of sterol regulatory element-binding protein-1c in mice: a novel peroxisome proliferator-activated receptor alpha-independent mechanism. Mol Pharmacol. 2009 Apr;75(4):782-92. doi: 10.1124/mol.108.052928. Epub 2009 Jan 5.
Ref 478 Pemafibrate: First Global Approval. Drugs. 2017 Oct;77(16):1805-1810. doi: 10.1007/s40265-017-0818-x.
Ref 479 Tesaglitazar, a dual PPAR-Alpha/Gamma agonist, hamster carcinogenicity, investigative animal and clinical studies. Toxicol Pathol. 2012;40(1):18-32. doi: 10.1177/0192623311429972. Epub 2011 Nov 30.
Ref 480 Ragaglitazar: the pharmacokinetics, pharmacodynamics, and tolerability of a novel dual PPAR alpha and gamma agonist in healthy subjects and patients with type 2 diabetes. J Clin Pharmacol. 2003 Nov;43(11):1244-56. doi: 10.1177/0091270003257230.
Ref 481 Tolerability and pharmacokinetics of lobeglitazone, a novel peroxisome proliferator-activated receptor-Gamma agonist, after a single oral administration in healthy female subjects. Clin Drug Investig. 2014 Jul;34(7):467-74. doi: 10.1007/s40261-014-0197-y.
Ref 482 Determination of chiglitazar, a dual alpha/gamma peroxisome proliferator-activated receptor (PPAR) agonist, in human plasma by liquid chromatography-tandem mass spectrometry. Pharmazie. 2007 Nov;62(11):825-9.
Ref 483 Pharmacokinetics, safety, and tolerability of saroglitazar (ZYH1), a predominantly PPARAlpha agonist with moderate PPARGamma agonist activity in healthy human subjects. Clin Drug Investig. 2013 Nov;33(11):809-16. doi: 10.1007/s40261-013-0128-3.
Ref 484 A novel oxyiminoalkanoic acid derivative, TAK-559, activates human peroxisome proliferator-activated receptor subtypes. Eur J Pharmacol. 2004 Jul 8;495(1):17-26. doi: 10.1016/j.ejphar.2004.05.020.
Ref 485 The disposition and metabolism of naveglitazar, a peroxisome proliferator-activated receptor alpha-gamma dual, gamma-dominant agonist in mice, rats, and monkeys. Drug Metab Dispos. 2007 Jan;35(1):51-61. doi: 10.1124/dmd.106.012328. Epub 2006 Sep 29.
Ref 486 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800024296)
Ref 487 Clinical pipeline report, company report or official report of Zydus Cadila.
Ref 488 Dual peroxisome proliferator-activated receptor Alpha/Delta agonist GFT505 improves hepatic and peripheral insulin sensitivity in abdominally obese subjects. Diabetes Care. 2013 Oct;36(10):2923-30. doi: 10.2337/dc12-2012. Epub 2013 May 28.
Ref 489 Mechanism of action of fibrates on lipid and lipoprotein metabolism. Circulation. 1998 Nov 10;98(19):2088-93. doi: 10.1161/01.cir.98.19.2088.
Ref 490 Therapeutic potential of aleglitazar, a new dual PPAR-Alpha/Gamma agonist: implications for cardiovascular disease in patients with diabetes mellitus. Am J Cardiovasc Drugs. 2010;10(4):209-16. doi: 10.2165/11539500-000000000-00000.
Ref 491 Clinical pipeline report, company report or official report of Tempest Therapeutics.
Ref 492 Design novel dual agonists for treating type-2 diabetes by targeting peroxisome proliferator-activated receptors with core hopping approach. PLoS One. 2012;7(6):e38546. doi: 10.1371/journal.pone.0038546. Epub 2012 Jun 7.
Ref 493 Potent and selective PPAR-alpha agonist LY518674 upregulates both ApoA-I production and catabolism in human subjects with the metabolic syndrome. Arterioscler Thromb Vasc Biol. 2009 Jan;29(1):140-6. doi: 10.1161/ATVBAHA.108.171223. Epub 2008 Nov 6.
Ref 494 Fibrates as therapy for osteoarthritis and rheumatoid arthritis A systematic review. Ther Adv Musculoskelet Dis. 2013 February; 5(1): 33-44.
Ref 495 Peroxisome proliferator-activated receptors, metabolic syndrome and cardiovascular disease. Future Cardiol. 2010 September; 6(5): 657-691.
Ref 496 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800021175)
Ref 497 Discovery of an oxybenzylglycine based peroxisome proliferator activated receptor alpha selective agonist 2-((3-((2-(4-chlorophenyl)-5-methyloxazol-4-yl)methoxy)benzyl)(methoxycarbonyl)amino)acetic acid (BMS-687453). J Med Chem. 2010 Apr 8;53(7):2854-64. doi: 10.1021/jm9016812.
Ref 498 Activation of peroxisome proliferator-activated receptor gamma (PPARgamma) by nitroalkene fatty acids: importance of nitration position and degree of unsaturation. J Med Chem. 2009 Aug 13;52(15):4631-9. doi: 10.1021/jm900326c.
Ref 499 Pharmacological profiles of a novel oral antidiabetic agent, JTT-501, an isoxazolidinedione derivative. Eur J Pharmacol. 1999 Jan 8;364(2-3):211-9. doi: 10.1016/s0014-2999(98)00832-2.
Ref 500 Molecular characterization of novel and selective peroxisome proliferator-activated receptor alpha agonists with robust hypolipidemic activity in vivo. Mol Pharmacol. 2009 Feb;75(2):296-306. doi: 10.1124/mol.108.051656. Epub 2008 Oct 29.
Ref 501 PPAR-alpha and -gamma but not -delta agonists inhibit airway inflammation in a murine model of asthma: in vitro evidence for an NF-kappaB-independent effect. Br J Pharmacol. 2003 May;139(1):163-71. doi: 10.1038/sj.bjp.0705232.
Ref 502 A new class of peroxisome proliferator-activated receptor agonists with a novel binding epitope shows antidiabetic effects. J Biol Chem. 2004 Sep 24;279(39):41124-30. doi: 10.1074/jbc.M401552200. Epub 2004 Jul 15.
Ref 503 Emerging antidyslipidemic drugs. Expert Opin Emerg Drugs. 2008 Jun;13(2):363-81. doi: 10.1517/14728214.13.2.363.
Ref 504 PPAR alpha structure-function relationships derived from species-specific differences in responsiveness to hypolipidemic agents. Biol Chem. 1997 Jul;378(7):651-5. doi: 10.1515/bchm.1997.378.7.651.
Ref 505 Design and synthesis of alpha-aryloxy-alpha-methylhydrocinnamic acids: a novel class of dual peroxisome proliferator-activated receptor alpha/gamma agonists. J Med Chem. 2004 May 6;47(10):2422-5. doi: 10.1021/jm0342616.
Ref 506 Phenylacetic acid derivatives as hPPAR agonists. Bioorg Med Chem Lett. 2003 Apr 7;13(7):1277-80. doi: 10.1016/s0960-894x(03)00115-x.
Ref 507 The ChEMBL database in 2017. Nucleic Acids Res. 2017 Jan 4;45(D1):D945-D954.
Ref 508 Oleoylethanolamide, an endogenous PPAR-alpha agonist, lowers body weight and hyperlipidemia in obese rats. Neuropharmacology. 2005 Jun;48(8):1147-53. doi: 10.1016/j.neuropharm.2005.02.013. Epub 2005 Apr 21.
Ref 509 Identification of a subtype selective human PPARalpha agonist through parallel-array synthesis. Bioorg Med Chem Lett. 2001 May 7;11(9):1225-7. doi: 10.1016/s0960-894x(01)00188-3.
Ref 510 Pristanic acid and phytanic acid: naturally occurring ligands for the nuclear receptor peroxisome proliferator-activated receptor alpha. J Lipid Res. 2000 Nov;41(11):1801-7.
Ref 511 A novel peroxisome proliferator-activated receptor alpha/gamma dual agonist demonstrates favorable effects on lipid homeostasis. Endocrinology. 2004 Apr;145(4):1640-8. doi: 10.1210/en.2003-1270. Epub 2003 Dec 30.
Ref 512 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Target id: 593).
Ref 513 Differential activation of peroxisome proliferator-activated receptors by eicosanoids. J Biol Chem. 1995 Oct 13;270(41):23975-83. doi: 10.1074/jbc.270.41.23975.
Ref 514 Antidiabetic and hypolipidemic potential of DRF 2519--a dual activator of PPAR-alpha and PPAR-gamma. Eur J Pharmacol. 2004 May 3;491(2-3):195-206. doi: 10.1016/j.ejphar.2004.03.034.
Ref 515 CN patent application no. 102459215, 3-(4-aminophenyl)-2-furancarboxylic acid derivative and pharmaceutically acceptable salt thereof.
Ref 516 Pharma & Vaccines. Product Development Pipeline. April 29 2009.
Ref 517 Docking and molecular dynamics simulations of peroxisome proliferator activated receptors interacting with pan agonist sodelglitazar. Protein Pept Lett. 2011 Oct;18(10):1021-7. doi: 10.2174/092986611796378701.
Ref 518 Identification of a functional peroxisome proliferator-activated receptor (PPAR) response element (PPRE) in the human apolipoprotein A-IV gene. Biochem Pharmacol. 2009 Sep 1;78(5):523-30. doi: 10.1016/j.bcp.2009.05.007. Epub 2009 May 9.
Ref 519 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800026848)
Ref 520 O-arylmandelic acids as highly selective human PPAR alpha/gamma agonists. Bioorg Med Chem Lett. 2003 Oct 6;13(19):3185-90. doi: 10.1016/s0960-894x(03)00702-9.
Ref 521 Discovery of cyclic amine-substituted benzoic acids as PPARAlpha agonists. Bioorg Med Chem Lett. 2012 Jan 1;22(1):334-8. doi: 10.1016/j.bmcl.2011.11.002. Epub 2011 Nov 9.
Ref 522 A peroxisome proliferator-activated receptor alpha/gamma dual agonist with a unique in vitro profile and potent glucose and lipid effects in rodent models of type 2 diabetes and dyslipidemia. Mol Endocrinol. 2005 Jun;19(6):1593-605. doi: 10.1210/me.2005-0015. Epub 2005 Apr 14.
Ref 523 Emerging drugs for non-alcoholic fatty liver disease. Expert Opin Emerg Drugs. 2008 Mar;13(1):145-58. doi: 10.1517/14728214.13.1.145.
Ref 524 Modulation of PPAR receptor subtype selectivity of the ligands: aliphatic chain vs aromatic ring as a spacer between pharmacophore and the lipophilic moiety. Bioorg Med Chem Lett. 2008 Dec 15;18(24):6471-5. doi: 10.1016/j.bmcl.2008.10.062. Epub 2008 Oct 17.
Ref 525 Cardiac function and metabolism in Type 2 diabetic mice after treatment with BM 17.0744, a novel PPAR-alpha activator. Am J Physiol Heart Circ Physiol. 2002 Sep;283(3):H949-57. doi: 10.1152/ajpheart.00226.2001.
Ref 526 CN patent application no. 1882326, Ppar agonists for the treatment of hcv infection.
Ref 527 CN patent application no. 100577175, Combination therapy comprising glucose reabsorption inhibitors and PPAR modulators.
Ref 528 Antidiabetic and hypolipidemic effects of a novel dual peroxisome proliferator-activated receptor (PPAR) alpha/gamma agonist, E3030, in db/db mice and beagle dogs. J Pharmacol Sci. 2008 Sep;108(1):40-8. doi: 10.1254/jphs.fp0072346. Epub 2008 Sep 6.
Ref 529 The peroxisome proliferator-activated receptor-alpha (PPAR-alpha) agonist, AVE8134, attenuates the progression of heart failure and increases survival in rats. Acta Pharmacol Sin. 2009 Jul;30(7):935-46. doi: 10.1038/aps.2009.58. Epub 2009 Jun 8.
Ref 530 DOI: 10.1038/scibx.2012.669
Ref 531 Peroxisome Proliferators-Activated Receptor (PPAR) Modulators and Metabolic Disorders. PPAR Res. 2008; 2008: 679137.
Ref 532 Scaffold-based discovery of indeglitazar, a PPAR pan-active anti-diabetic agent. Proc Natl Acad Sci U S A. 2009 Jan 6;106(1):262-7. doi: 10.1073/pnas.0811325106. Epub 2008 Dec 30.
Ref 533 Hypoxia-inducible factor (HIF) inhibitors: a patent survey (2011-2015). Expert Opin Ther Pat. 2016;26(3):309-22. doi: 10.1517/13543776.2016.1146252. Epub 2016 Feb 16.
Ref 534 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2019
Ref 535 Targeting the phosphoinositide 3-kinase pathway in cancer. Nat Rev Drug Discov. 2009 Aug;8(8):627-44. doi: 10.1038/nrd2926.
Ref 536 Company report (BioOncology)
Ref 537 Company report (Lilly)
Ref 538 ETP-46321, a dual p110Alpha/Delta class IA phosphoinositide 3-kinase inhibitor modulates T lymphocyte activation and collagen-induced arthritis. Biochem Pharmacol. 2016 Apr 15;106:56-69. doi: 10.1016/j.bcp.2016.02.005. Epub 2016 Feb 13.
Ref 539 National Cancer Institute Drug Dictionary (drug id 714372).
Ref 540 Adaptive resistance to PI3KAlpha-selective inhibitor CYH33 is mediated by genomic and transcriptomic alterations in ESCC cells. Cell Death Dis. 2021 Jan 14;12(1):85. doi: 10.1038/s41419-020-03370-4.
Ref 541 In vitro anticancer activity of PI3K alpha selective inhibitor BYL719 in head and neck cancer. Anticancer Res. 2015 Jan;35(1):175-82.
Ref 542 N(6)-methyladenosine mRNA methylation of PIK3CB regulates AKT signalling to promote PTEN-deficient pancreatic cancer progression. Gut. 2020 Dec;69(12):2180-2192. doi: 10.1136/gutjnl-2019-320179. Epub 2020 Apr 20.
Ref 543 1-substituted (Dibenzo[b,d]thiophen-4-yl)-2-morpholino-4H-chromen-4-ones endowed with dual DNA-PK/PI3-K inhibitory activity. J Med Chem. 2013 Aug 22;56(16):6386-401. doi: 10.1021/jm400915j. Epub 2013 Aug 1.
Ref 544 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 7967).
Ref 545 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Target id: 2154).
Ref 546 Over-expression of clusterin is a resistance factor to the anti-cancer effect of histone deacetylase inhibitors. Eur J Cancer. 2009 Jul;45(10):1846-54. doi: 10.1016/j.ejca.2009.03.002. Epub 2009 Apr 1.
Ref 547 Synthesis and biological evaluation of sulfonylhydrazone-substituted imidazo[1,2-a]pyridines as novel PI3 kinase p110alpha inhibitors. Bioorg Med Chem. 2007 Sep 1;15(17):5837-44. doi: 10.1016/j.bmc.2007.05.070. Epub 2007 Jun 6.
Ref 548 US patent application no. 6,133,032, Antisense modulation of PI3 kinase p110 beta expression.
Ref 549 LY294002-geldanamycin heterodimers as selective inhibitors of the PI3K and PI3K-related family. Bioorg Med Chem Lett. 2001 Apr 9;11(7):909-13. doi: 10.1016/s0960-894x(01)00099-3.
Ref 550 PI 3-kinase p110beta: a new target for antithrombotic therapy. Nat Med. 2005 May;11(5):507-14. doi: 10.1038/nm1232. Epub 2005 Apr 17.
Ref 551 Human target validation of phosphoinositide 3-kinase (PI3K)beta: effects on platelets and insulin sensitivity, using AZD6482 a novel PI3Kbeta inhibitor. J Thromb Haemost. 2012 Oct;10(10):2127-36.
Ref 552 Inactivation of PI(3)K p110Delta breaks regulatory T-cell-mediated immune tolerance to cancer. Nature. 2014 Jun 19;510(7505):407-411. doi: 10.1038/nature13444. Epub 2014 Jun 11.
Ref 553 m(6) A deposition is regulated by PRMT1-mediated arginine methylation of METTL14 in its disordered C-terminal region. EMBO J. 2021 Mar 1;40(5):e106309. doi: 10.15252/embj.2020106309. Epub 2021 Jan 18.
Ref 554 Clinical and pharmacological phase I evaluation of Exherin (ADH-1), a selective anti-N-cadherin peptide in patients with N-cadherin-expressing solid tumours. Ann Oncol. 2009 Apr;20(4):741-5. doi: 10.1093/annonc/mdn695. Epub 2009 Feb 3.
Ref 555 National Cancer Institute Drug Dictionary (drug name GSK6097608).
Ref 556 Small molecule regulators of protein arginine methyltransferases. J Biol Chem. 2004 Jun 4;279(23):23892-9. doi: 10.1074/jbc.M401853200. Epub 2004 Mar 31.
Ref 557 The selective hypoxia inducible factor-1 inhibitor PX-478 provides in vivo radiosensitization through tumor stromal effects. Mol Cancer Ther. 2009 Apr;8(4):947-58. doi: 10.1158/1535-7163.MCT-08-0981.
Ref 558 Local delivery of c-myc neutrally charged antisense oligonucleotides with transport catheter inhibits myointimal hyperplasia and positively affects vascular remodeling in the rabbit balloon injury model. Catheter Cardiovasc Interv. 2001 Oct;54(2):247-56. doi: 10.1002/ccd.1277.
Ref 559 Liposarcoma: molecular genetics and therapeutics. Sarcoma. 2011;2011:483154. doi: 10.1155/2011/483154. Epub 2010 Dec 27.
Ref 560 Discovery of a 2,4-disubstituted pyrrolo[1,2-f][1,2,4]triazine inhibitor (BMS-754807) of insulin-like growth factor receptor (IGF-1R) kinase in clinical development. J Med Chem. 2009 Dec 10;52(23):7360-3. doi: 10.1021/jm900786r.
Ref 561 CenterWatch. Drugs in Clinical Trials Database. CenterWatch. 2008.
Ref 562 Pre-clinical and Clinical Safety Studies of CMX-2043: a cytoprotective lipoic acid analogue for ischaemia-reperfusion injury. Basic Clin Pharmacol Toxicol. 2014 Nov;115(5):456-64. doi: 10.1111/bcpt.12254. Epub 2014 May 16.
Ref 563 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Target id: 1479).
Ref 564 Cancer stem cell (CSC) inhibitors: a review of recent patents (2012-2015). Expert Opin Ther Pat. 2017 Jul;27(7):753-761. doi: 10.1080/13543776.2017.1325465. Epub 2017 May 5.
Ref 565 2,3,5-Trisubstituted pyridines as selective AKT inhibitors. Part II: Improved drug-like properties and kinase selectivity from azaindazoles. Bioorg Med Chem Lett. 2010 Jan 15;20(2):679-83. doi: 10.1016/j.bmcl.2009.11.060. Epub 2009 Nov 20.
Ref 566 Comprehensive analysis of kinase inhibitor selectivity. Nat Biotechnol. 2011 Oct 30;29(11):1046-51. doi: 10.1038/nbt.1990.
Ref 567 Indolinone based phosphoinositide-dependent kinase-1 (PDK1) inhibitors. Part 1: design, synthesis and biological activity. Bioorg Med Chem Lett. 2007 Jul 15;17(14):3814-8. doi: 10.1016/j.bmcl.2007.04.071. Epub 2007 Apr 27.
Ref 568 The PI3K/Akt pathway as a target in the treatment of hematologic malignancies. Anticancer Agents Med Chem. 2009 Jun;9(5):550-9. doi: 10.2174/187152009788451851.
Ref 569 Identification of 4-(2-(4-amino-1,2,5-oxadiazol-3-yl)-1-ethyl-7-{[(3S)-3-piperidinylmethyl]oxy}-1H-imidazo[4,5-c]pyridin-4-yl)-2-methyl-3-butyn-2-ol (GSK690693), a novel inhibitor of AKT kinase. J Med Chem. 2008 Sep 25;51(18):5663-79. doi: 10.1021/jm8004527.
Ref 570 Raft nanodomains contribute to Akt/PKB plasma membrane recruitment and activation. Nat Chem Biol. 2008 Sep;4(9):538-47. doi: 10.1038/nchembio.103. Epub 2008 Jul 20.
Ref 571 A phthalide with in vitro growth inhibitory activity from an oidiodendron strain. J Nat Prod. 2004 Dec;67(12):2086-9. doi: 10.1021/np040123n.
Ref 572 N (6)-Methyladenosine modification of hepatitis B and C viral RNAs attenuates host innate immunity via RIG-I signaling. J Biol Chem. 2020 Sep 11;295(37):13123-13133. doi: 10.1074/jbc.RA120.014260. Epub 2020 Jul 27.
Ref 573 DNA methyltransferase inhibitors: an updated patent review (2012-2015). Expert Opin Ther Pat. 2016 Sep;26(9):1017-30. doi: 10.1080/13543776.2016.1209488. Epub 2016 Jul 18.
Ref 574 Company reprot (Spring Bank Pharmaceuticals) (drug: SB 9200)
Ref 575 Clinical pipeline report, company report or official report of CureVac.
Ref 576 The m6A methyltransferase METTL14 inhibits the proliferation, migration, and invasion of gastric cancer by regulating the PI3K/AKT/mTOR signaling pathway. J Clin Lab Anal. 2021 Mar;35(3):e23655. doi: 10.1002/jcla.23655. Epub 2020 Dec 12.
Ref 577 Hedgehog inhibitors: a patent review (2013 - present). Expert Opin Ther Pat. 2015 May;25(5):549-65. doi: 10.1517/13543776.2015.1019864. Epub 2015 Mar 1.
Ref 578 [Mammalian target of rapamycin, its mode of action and clinical response in metastatic clear cell carcinoma]. Gan To Kagaku Ryoho. 2009 Jul;36(7):1076-9.
Ref 579 Advances in kinase targeting: current clinical use and clinical trials. Trends Pharmacol Sci. 2014 Nov;35(11):604-20. doi: 10.1016/j.tips.2014.09.007. Epub 2014 Oct 10.
Ref 580 A novel c-Met inhibitor, MK8033, synergizes with carboplatin plus paclitaxel to inhibit ovarian cancer cell growth. Oncol Rep. 2013 May;29(5):2011-8. doi: 10.3892/or.2013.2329. Epub 2013 Mar 5.
Ref 581 Simultaneous targeting of PI3K and mTOR with NVP-BGT226 is highly effective in multiple myeloma. Anticancer Drugs. 2012 Jan;23(1):131-8. doi: 10.1097/CAD.0b013e32834c8683.
Ref 582 Dramatic suppression of colorectal cancer cell growth by the dual mTORC1 and mTORC2 inhibitor AZD-2014. Biochem Biophys Res Commun. 2014 Jan 10;443(2):406-12. doi: 10.1016/j.bbrc.2013.11.099. Epub 2013 Dec 2.
Ref 583 PF-04691502, a potent and selective oral inhibitor of PI3K and mTOR kinases with antitumor activity. Mol Cancer Ther. 2011 Nov;10(11):2189-99. doi: 10.1158/1535-7163.MCT-11-0185. Epub 2011 Jul 12.
Ref 584 CC-223, a Potent and Selective Inhibitor of mTOR Kinase: In Vitro and In Vivo Characterization. Mol Cancer Ther. 2015 Jun;14(6):1295-305. doi: 10.1158/1535-7163.MCT-14-1052. Epub 2015 Apr 8.
Ref 585 2011 Pipeline of Intellikine.
Ref 586 The dual PI3K/mTOR inhibitor NVP-BEZ235 is a potent inhibitor of ATM- and DNA-PKCs-mediated DNA damage responses. Neoplasia. 2012 Jan;14(1):34-43.
Ref 587 First-in-Human Study of PF-05212384 (PKI-587), a Small-Molecule, Intravenous, Dual Inhibitor of PI3K and mTOR in Patients with Advanced Cancer. Clin Cancer Res. 2015 Apr 15;21(8):1888-95. doi: 10.1158/1078-0432.CCR-14-1306. Epub 2015 Feb 4.
Ref 588 A first-in-human Phase I study of DS-3078a, an oral TORC1/2 inhibitor, in patients with advanced solid tumors: Preliminary results, Mol Cancer Ther November,2013, 12, C173.
Ref 589 Discovery and Biological Profiling of Potent and Selective mTOR Inhibitor GDC-0349. ACS Med Chem Lett. 2012 Nov 29;4(1):103-7. doi: 10.1021/ml3003132. eCollection 2013 Jan 10.
Ref 590 PIK3CA mutation H1047R is associated with response to PI3K/AKT/mTOR signaling pathway inhibitors in early phase clinical trials
Ref 591 National Cancer Institute Drug Dictionary (drug id 728650).
Ref 592 Antitumor activity and induction of TP53-dependent apoptosis toward ovarian clear cell adenocarcinoma by the dual PI3K/mTOR inhibitor DS-7423. PLoS One. 2014 Feb 4;9(2):e87220. doi: 10.1371/journal.pone.0087220. eCollection 2014.
Ref 593 Novel purine and pyrazolo[3,4-d]pyrimidine inhibitors of PI3 kinase-alpha: Hit to lead studies. Bioorg Med Chem Lett. 2010 Jan 15;20(2):636-9. doi: 10.1016/j.bmcl.2009.11.051. Epub 2009 Dec 5.
Ref 594 The rapamycin-binding domain of the protein kinase mammalian target of rapamycin is a destabilizing domain. J Biol Chem. 2007 May 4;282(18):13395-401. doi: 10.1074/jbc.M700498200. Epub 2007 Mar 9.
Ref 595 Torin2 Potentiates Anticancer Effects on Adult T-Cell Leukemia/Lymphoma by Inhibiting Mammalian Target of Rapamycin. Anticancer Res. 2016 Jan;36(1):95-102.
Ref 596 Selective benzopyranone and pyrimido[2,1-a]isoquinolin-4-one inhibitors of DNA-dependent protein kinase: synthesis, structure-activity studies, and radiosensitization of a human tumor cell line in vitro. J Med Chem. 2005 Jan 27;48(2):569-85. doi: 10.1021/jm049526a.
Ref 597 Synthesis and therapeutic evaluation of pyridyl based novel mTOR inhibitors. Bioorg Med Chem Lett. 2009 Jun 1;19(11):2949-52. doi: 10.1016/j.bmcl.2009.04.055. Epub 2009 Apr 18.
Ref 598 Discovery of 1-(4-(4-propionylpiperazin-1-yl)-3-(trifluoromethyl)phenyl)-9-(quinolin-3-yl)benzo[h][1,6]naphthyridin-2(1H)-one as a highly potent, selective mammalian target of rapamycin (mTOR) inhibitor for the treatment of cancer. J Med Chem. 2010 Oct 14;53(19):7146-55. doi: 10.1021/jm101144f.
Ref 599 Genta obtains orphan drug designation for C-Myb Antisense (LR3001) in chronic myelocytic leukemia. Genta. 2005.
Ref 600 Discovery of the Highly Potent PI3K/mTOR Dual Inhibitor PF-04979064 through Structure-Based Drug Design. ACS Med Chem Lett. 2012 Nov 7;4(1):91-7. doi: 10.1021/ml300309h. eCollection 2013 Jan 10.
Ref 601 Early detection of response to experimental chemotherapeutic Top216 with [18F]FLT and [18F]FDG PET in human ovary cancer xenografts in mice. PLoS One. 2010 Sep 24;5(9):e12965. doi: 10.1371/journal.pone.0012965.
Ref 602 Clinical pipeline report, company report or official report of tatcongress.
Ref 603 EP patent application no. 2275103, Mtor inhibitors in the treatment of endocrine tumors.
Ref 604 Clinical pipeline report, company report or official report of AstraZeneca (2009).
Ref 605 A STAT inhibitor patent review: progress since 2011.Expert Opin Ther Pat. 2015;25(12):1397-421.
Ref 606 The human sulfatase 2 inhibitor 2,4-disulfonylphenyl-tert-butylnitrone (OKN-007) has an antitumor effect in hepatocellular carcinoma mediated via suppression of TGFB1/SMAD2 and Hedgehog/GLI1 signaling. Genes Chromosomes Cancer. 2013 Mar;52(3):225-36. doi: 10.1002/gcc.22022. Epub 2012 Oct 29.
Ref 607 Hepcidin agonists as therapeutic tools. Blood. 2018 Apr 19;131(16):1790-1794. doi: 10.1182/blood-2017-11-737411. Epub 2018 Mar 9.
Ref 608 Targeting the Hepcidin-Ferroportin Axis to Develop New Treatment Strategies for Anemia of Chronic Disease and Anemia of Inflammation. Am J Hematol. 2012 April; 87(4): 392-400.
Ref 609 Piperazine derivatives for treating disorders. US9695160.
Ref 610 m(6)A mRNA methylation regulates AKT activity to promote the proliferation and tumorigenicity of endometrial cancer. Nat Cell Biol. 2018 Sep;20(9):1074-1083. doi: 10.1038/s41556-018-0174-4. Epub 2018 Aug 27.
Ref 611 METTL14 promotes prostate tumorigenesis by inhibiting THBS1 via an m6A-YTHDF2-dependent mechanism. Cell Death Discov. 2022 Mar 30;8(1):143. doi: 10.1038/s41420-022-00939-0.
Ref 612 Clinical pipeline report, company report or official report of Immune-Onc Therapeutics.
Ref 613 A phase II study of ABT-510 (thrombospondin-1 analog) for the treatment of metastatic melanoma. Am J Clin Oncol. 2007 Jun;30(3):303-9. doi: 10.1097/01.coc.0000256104.80089.35.
Ref 614 Species- or isozyme-specific enzyme inhibitors. 5. Differential effects of thymidine substituents on affinity for rat thymidine kinase isozymes. J Med Chem. 1982 Jun;25(6):644-9. doi: 10.1021/jm00348a007.
Ref 615 Company report (Takara Bio)
Ref 616 Specific recognition of the bicyclic pyrimidine nucleoside analogs, a new class of highly potent and selective inhibitors of varicella-zoster virus (VZV), by the VZV-encoded thymidine kinase. Mol Pharmacol. 2002 Feb;61(2):249-54. doi: 10.1124/mol.61.2.249.
Ref 617 Pronounced antitumor effects and tumor radiosensitization of double suicide gene therapy. Clin Cancer Res. 1997 Nov;3(11):2081-8.
Ref 618 DrugBank 3.0: a comprehensive resource for 'omics' research on drugs. Nucleic Acids Res. 2011 Jan;39(Database issue):D1035-41. doi: 10.1093/nar/gkq1126. Epub 2010 Nov 8.
Ref 619 Induction of the Epstein-Barr virus thymidine kinase gene with concomitant nucleoside antivirals as a therapeutic strategy for Epstein-Barr virus-associated malignancies. Curr Opin Oncol. 2001 Sep;13(5):360-7. doi: 10.1097/00001622-200109000-00008.
Ref 620 N1-substituted thymine derivatives as mitochondrial thymidine kinase (TK-2) inhibitors. J Med Chem. 2006 Dec 28;49(26):7766-73. doi: 10.1021/jm0610550.
Ref 621 Synthesis, in vitro, and in silico evaluation of organometallic technetium and rhenium thymidine complexes with retained substrate activity toward human thymidine kinase type 1. J Med Chem. 2008 Nov 13;51(21):6689-98. doi: 10.1021/jm800530p. Epub 2008 Oct 7.
Ref 622 Sitimagene ceradenovec: a gene-based drug for the treatment of operable high-grade glioma. Future Oncol. 2010 Nov;6(11):1691-710. doi: 10.2217/fon.10.134.
Ref 623 Sensitivity of monkey B virus (Cercopithecine herpesvirus 1) to antiviral drugs: role of thymidine kinase in antiviral activities of substrate analogs and acyclonucleosides. Antimicrob Agents Chemother. 2007 Jun;51(6):2028-34. doi: 10.1128/AAC.01284-06. Epub 2007 Apr 16.
Ref 624 Crystal structure of varicella zoster virus thymidine kinase. J Biol Chem. 2003 Jul 4;278(27):24680-7. doi: 10.1074/jbc.M302025200. Epub 2003 Apr 9.
Ref 625 Trichomonas vaginalis thymidine kinase: purification, characterization and search for inhibitors. Biochem J. 1998 Aug 15;334 ( Pt 1)(Pt 1):15-22. doi: 10.1042/bj3340015.
Ref 626 3'-[4-Aryl-(1,2,3-triazol-1-yl)]-3'-deoxythymidine analogues as potent and selective inhibitors of human mitochondrial thymidine kinase. J Med Chem. 2010 Apr 8;53(7):2902-12. doi: 10.1021/jm901532h.
Ref 627 Phase I dose escalation clinical trial of adenovirus vector carrying osteocalcin promoter-driven herpes simplex virus thymidine kinase in localized and metastatic hormone-refractory prostate cancer. Hum Gene Ther. 2003 Feb 10;14(3):227-41. doi: 10.1089/10430340360535788.
Ref 628 METTL14 promotes glomerular endothelial cell injury and diabetic nephropathy via m6A modification of Alpha-klotho. Mol Med. 2021 Sep 9;27(1):106. doi: 10.1186/s10020-021-00365-5.
Ref 629 Targeted therapies in myelodysplastic syndromes: ASH 2003 review. Semin Hematol. 2004 Apr;41(2 Suppl 4):13-20. doi: 10.1053/j.seminhematol.2004.02.003.
Ref 630 Thalidomide and thalidomide analogues for maintenance of remission in Crohn's disease. Cochrane Database Syst Rev. 2009 Apr 15;2009(2):CD007351. doi: 10.1002/14651858.CD007351.pub2.
Ref 631 The potential of biologics for the treatment of asthma. Nat Rev Drug Discov. 2012 Dec;11(12):958-72. doi: 10.1038/nrd3792.
Ref 632 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2019
Ref 633 Oral pentoxifylline inhibits release of tumor necrosis factor-alpha from human peripheral blood monocytes : a potential treatment for aseptic loosening of total joint components. J Bone Joint Surg Am. 2001 Jul;83(7):1057-61. doi: 10.2106/00004623-200107000-00012.
Ref 634 [Efficacy of different thalidomide regimens for patients with multiple myeloma and its relationship with TNF-alpha level]. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2008 Dec;16(6):1312-5.
Ref 635 2009 FDA drug approvals. Nat Rev Drug Discov. 2010 Feb;9(2):89-92. doi: 10.1038/nrd3101.
Ref 636 Emerging drugs for rheumatoid arthritis. Expert Opin Emerg Drugs. 2008 Mar;13(1):175-96. doi: 10.1517/14728214.13.1.175.
Ref 637 Drug insight: tumor necrosis factor-converting enzyme as a pharmaceutical target for rheumatoid arthritis. Nat Clin Pract Rheumatol. 2008 Jun;4(6):300-9. doi: 10.1038/ncprheum0797. Epub 2008 Apr 15.
Ref 638 Apoptosis and the FLIP and NF-kappa B proteins as pharmacodynamic criteria for biosimilar TNF-alpha antagonists. Biologics. 2014 Jul 31;8:211-20. doi: 10.2147/BTT.S57253. eCollection 2014.
Ref 639 Biosimilars in the therapy of inflammatory bowel diseases. Eur J Gastroenterol Hepatol. 2014 Jun;26(6):581-7. doi: 10.1097/MEG.0000000000000098.
Ref 640 Adalimumab for psoriasis patients who are non-responders to etanercept: open-label prospective evaluation. J Eur Acad Dermatol Venereol. 2009 Dec;23(12):1394-7. doi: 10.1111/j.1468-3083.2009.03325.x. Epub 2009 Jul 1.
Ref 641 TNFerade, an adenovector carrying the transgene for human tumor necrosis factor alpha, for patients with advanced solid tumors: surgical experience and long-term follow-up. Ann Surg Oncol. 2005 Oct;12(10):825-30. doi: 10.1245/ASO.2005.03.023. Epub 2005 Aug 9.
Ref 642 Case study: biosimilar anti TNFalpha (Adalimumab) analysis of Fc effector functions. BMC Proc. 2013; 7(Suppl 6): P30.
Ref 643 Emerging drugs in neuropathic pain. Expert Opin Emerg Drugs. 2007 Mar;12(1):113-26. doi: 10.1517/14728214.12.1.113.
Ref 644 RDP58, a locally active TNF inhibitor, is effective in the dextran sulphate mouse model of chronic colitis. Inflamm Res. 2002 Nov;51(11):522-31. doi: 10.1007/pl00012423.
Ref 645 Diabetes-enhanced tumor necrosis factor-alpha production promotes apoptosis and the loss of retinal microvascular cells in type 1 and type 2 models of diabetic retinopathy. Am J Pathol. 2008 May;172(5):1411-8. doi: 10.2353/ajpath.2008.071070. Epub 2008 Apr 10.
Ref 646 AP301, a synthetic peptide mimicking the lectin-like domain of TNF, enhances amiloride-sensitive Na(+) current in primary dog, pig and rat alveolar type II cells. Pulm Pharmacol Ther. 2013 Jun;26(3):356-63. doi: 10.1016/j.pupt.2012.12.011. Epub 2013 Jan 9.
Ref 647 Discovery of the inhibitors of tumor necrosis factor alpha with structure-based virtual screening. Bioorg Med Chem Lett. 2010 Nov 1;20(21):6195-8. doi: 10.1016/j.bmcl.2010.08.116. Epub 2010 Sep 16.
Ref 648 Modulation of Anti-Tumor Necrosis Factor Alpha (TNF-alpha) Antibody Secretion in Mice Immunized with TNF-alpha Kinoid. Clin Vaccine Immunol. 2012 May; 19(5): 699-703.
Ref 649 Cyclic AMP inhibition of tumor necrosis factor alpha production induced by amyloidogenic C-terminal peptide of Alzheimer's amyloid precursor protein in macrophages: involvement of multiple intracellular pathways and cyclic AMP response element binding protein. Mol Pharmacol. 2003 Mar;63(3):690-8. doi: 10.1124/mol.63.3.690.
Ref 650 DOI: 10.1136/annrheumdis-2015-eular.4042
Ref 651 Inhibition of experimental periodontitis by a topical boron-based antimicrobial. J Dent Res. 2008 Feb;87(2):148-52. doi: 10.1177/154405910808700208.
Ref 652 Pharmacokinetics and posterior segment biodistribution of ESBA105, an anti-TNF-alpha single-chain antibody, upon topical administration to the rabbit eye. Invest Ophthalmol Vis Sci. 2009 Feb;50(2):771-8. doi: 10.1167/iovs.08-2370. Epub 2008 Aug 29.
Ref 653 New developments in immunosuppressive therapy for heart transplantation. Expert Opin Emerg Drugs. 2009 Mar;14(1):1-21. doi: 10.1517/14728210902791605.
Ref 654 Clinical pipeline report, company report or official report of INmune Bio.
Ref 655 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800033173)
Ref 656 Emerging drugs for psoriasis. Expert Opin Emerg Drugs. 2009 Mar;14(1):145-63. doi: 10.1517/14728210902771334.
Ref 657 Phase I and Pharmacokinetic Studies of CYT-6091, a Novel PEGylated Colloidal Gold-rhTNF Nanomedicine. Clin Cancer Res. 2010 December 15; 16(24): 6139-6149.
Ref 658 A novel anti-rheumatic drug suppresses tumor necrosis factor-alpha and augments interleukin-10 in adjuvant arthritic rats. Eur J Pharmacol. 2000 Dec 15;409(3):331-5. doi: 10.1016/s0014-2999(00)00866-9.
Ref 659 Therapeutic Vaccination with TNF-Kinoid in TNF Antagonist-Resistant Rheumatoid Arthritis: A Phase II Randomized, Controlled Clinical Trial. PLoS One. 2014; 9(12): e113465.
Ref 660 Beta-aryl-succinic acid hydroxamates as dual inhibitors of matrix metalloproteinases and tumor necrosis factor alpha converting enzyme. J Med Chem. 2002 May 23;45(11):2289-93. doi: 10.1021/jm0110993.
Ref 661 Discovery of gamma-lactam hydroxamic acids as selective inhibitors of tumor necrosis factor alpha converting enzyme: design, synthesis, and structure-activity relationships. J Med Chem. 2002 Nov 7;45(23):4954-7. doi: 10.1021/jm0255670.
Ref 662 IND Filed for AME-527, Monoclonal Antibody That Is a Potential Treatment for Rheumatoid Arthritis. P&T Community. 2015.
Ref 663 Randomized, placebo-controlled trial of the anti-tumor necrosis factor antibody fragment afelimomab in hyperinflammatory response during severe sepsis: The RAMSES Study. Crit Care Med. 2001 Apr;29(4):765-9. doi: 10.1097/00003246-200104000-00015.
Ref 664 US patent application no. 2008,0269,123, Methods for treating polycystic kidney disease (pkd) or other cyst forming diseases.
Ref 665 AGIX-4207 [2-[4-[[1-[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]thio]-1-methylethyl]thio]-2,6-bis(1,1-dimethylethyl)phenoxy]acetic acid], a novel antioxidant and anti-inflammatory compound: cellular and biochemical characterization of antioxidant activity and inhibition of redox-sensitive inflammatory gene expression. J Pharmacol Exp Ther. 2005 May;313(2):492-501. doi: 10.1124/jpet.104.080804. Epub 2005 Feb 8.
Ref 666 US patent application no. 8007,790, Methods for treating polycystic kidney disease (pkd) or other cyst forming diseases.
Ref 667 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Target id: 2608).
Ref 668 Effect of FR133605, a novel cytokine suppressive agent, on bone and cartilage destruction in adjuvant arthritic rats. J Rheumatol. 1996 Oct;23(10):1778-83.
Ref 669 CDP571, a humanized monoclonal antibody to tumour necrosis factor-alpha, for steroid-dependent Crohn's disease: a randomized, double-blind, placebo-controlled trial. Aliment Pharmacol Ther. 2006 Mar 1;23(5):617-28. doi: 10.1111/j.1365-2036.2006.02791.x.
Ref 670 Effect of the carbocyclic nucleoside analogue MDL 201,112 on inhibition of interferon-gamma-induced priming of Lewis (LEW/N) rat macrophages for enhanced respiratory burst and MHC class II Ia+ antigen expression. J Leukoc Biol. 1994 Aug;56(2):133-44. doi: 10.1002/jlb.56.2.133.
Ref 671 N(6)-Methyladenosines Modulate A-to-I RNA Editing. Mol Cell. 2018 Jan 4;69(1):126-135.e6. doi: 10.1016/j.molcel.2017.12.006.
Ref 672 Identification of new inhibitors of protein kinase R guided by statistical modeling. Bioorg Med Chem Lett. 2011 Jul 1;21(13):4108-14. doi: 10.1016/j.bmcl.2011.04.149. Epub 2011 May 13.
Ref 673 Heterocycle-substituted pyridyl benzothiophenes as kinase inhibitors. US9650366.
Ref 674 hsa-miR-191 is a candidate oncogene target for hepatocellular carcinoma therapy. Cancer Res. 2010 Oct 15;70(20):8077-87. doi: 10.1158/0008-5472.CAN-10-1313. Epub 2010 Oct 5.
Ref 675 MI-219-zinc combination: a new paradigm in MDM2 inhibitor-based therapy. Oncogene. 2011 Jan 6;30(1):117-26. doi: 10.1038/onc.2010.403. Epub 2010 Sep 6.
Ref 676 Pre-clinical evaluation of the MDM2-p53 antagonist RG7388 alone and in combination with chemotherapy in neuroblastoma. Oncotarget. 2015 Apr 30;6(12):10207-21. doi: 10.18632/oncotarget.3504.
Ref 677 Discovery of a small molecule MDM2 inhibitor (AMG 232) for treating cancer. J Med Chem. 2014 Aug 14;57(15):6332-41. doi: 10.1021/jm500627s. Epub 2014 Jul 9.
Ref 678 Clinical pipeline report, company report or official report of Astex Pharmaceuticals.
Ref 679 Serdemetan antagonizes the Mdm2-HIF1Alpha axis leading to decreased levels of glycolytic enzymes. PLoS One. 2013 Sep 6;8(9):e74741. doi: 10.1371/journal.pone.0074741. eCollection 2013.
Ref 680 MDM2 inhibition: an important step forward in cancer therapy. Leukemia. 2020 Nov;34(11):2858-2874. doi: 10.1038/s41375-020-0949-z. Epub 2020 Jul 10.
Ref 681 Drugging the p53 pathway: understanding the route to clinical efficacy. Nat Rev Drug Discov. 2014 Mar;13(3):217-36. doi: 10.1038/nrd4236.
Ref 682 Phase I clinical trail of RG7775 for treating Acute myelogenous leukemia. Roche.
Ref 683 Clinical pipeline report, company report or official report of Hygeia Therapeutics.
Ref 684 Reaching for high-hanging fruit in drug discovery at protein-protein interfaces. Nature. 2007 Dec 13;450(7172):1001-9. doi: 10.1038/nature06526.
Ref 685 Structure-based design of spiro-oxindoles as potent, specific small-molecule inhibitors of the MDM2-p53 interaction. J Med Chem. 2006 Jun 15;49(12):3432-5. doi: 10.1021/jm051122a.
Ref 686 Discovery of a nanomolar inhibitor of the human murine double minute 2 (MDM2)-p53 interaction through an integrated, virtual database screening strategy. J Med Chem. 2006 Jun 29;49(13):3759-62. doi: 10.1021/jm060023+.
Ref 687 A novel arginine methyltransferase inhibitor with cellular activity. Bioorg Med Chem Lett. 2007 Aug 1;17(15):4150-3. doi: 10.1016/j.bmcl.2007.05.088. Epub 2007 Jun 3.