General Information of the m6A Regulator (ID: REG00005)
Regulator Name RNA demethylase ALKBH5 (ALKBH5)
Synonyms
Alkylated DNA repair protein alkB homolog 5; Alpha-ketoglutarate-dependent dioxygenase alkB homolog 5; ABH5; OFOXD1
    Click to Show/Hide
Gene Name ALKBH5
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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) 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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ABT-737 through regulating the expression of Apoptosis regulator Bcl-2 (BCL-2). [1], [29]
Aurora kinase B (AURKB)
AT9283 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for AT9283. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AT9283 through regulating the expression of Aurora kinase B (AURKB). [30], [31]
ABT-348 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for ABT-348. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ABT-348 through regulating the expression of Aurora kinase B (AURKB). [30], [32]
PHA-739358 [Phase 2]
In total 2 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for PHA-739358. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PHA-739358 through regulating the expression of Aurora kinase B (AURKB). [30], [31]
Aurora kinase B (AURKB) is a therapeutic target for PHA-739358. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PHA-739358 through regulating the expression of Aurora kinase B (AURKB). [30], [33]
VX-680 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for VX-680. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of VX-680 through regulating the expression of Aurora kinase B (AURKB). [30], [34]
AMG 900 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for AMG 900. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AMG 900 through regulating the expression of Aurora kinase B (AURKB). [30], [35]
AZD-1152-HQPA [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for AZD-1152-HQPA. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AZD-1152-HQPA through regulating the expression of Aurora kinase B (AURKB). [30], [36]
BI-811283 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for BI-811283. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BI-811283 through regulating the expression of Aurora kinase B (AURKB). [30], [37]
BI-831266 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for BI-831266. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BI-831266 through regulating the expression of Aurora kinase B (AURKB). [30], [38]
BI-847325 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for BI-847325. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BI-847325 through regulating the expression of Aurora kinase B (AURKB). [30], [39]
CYC116 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for CYC116. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CYC116 through regulating the expression of Aurora kinase B (AURKB). [30], [40]
GSK1070916 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for GSK1070916. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of GSK1070916 through regulating the expression of Aurora kinase B (AURKB). [30], [39]
GSK1070916A [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for GSK1070916A. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of GSK1070916A through regulating the expression of Aurora kinase B (AURKB). [30], [41]
HPP-607 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for HPP-607. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of HPP-607 through regulating the expression of Aurora kinase B (AURKB). [30], [42]
MK-5108 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for MK-5108. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of MK-5108 through regulating the expression of Aurora kinase B (AURKB). [30], [43]
R763 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for R763. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of R763 through regulating the expression of Aurora kinase B (AURKB). [30], [44]
SNS-314 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for SNS-314. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of SNS-314 through regulating the expression of Aurora kinase B (AURKB). [30], [45]
TAK-901 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for TAK-901. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of TAK-901 through regulating the expression of Aurora kinase B (AURKB). [30], [46]
4-(1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for 4-(1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridine. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 4-(1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridine through regulating the expression of Aurora kinase B (AURKB). [30], [47]
6-bromoindirubin-3-oxime [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for 6-bromoindirubin-3-oxime. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 6-bromoindirubin-3-oxime through regulating the expression of Aurora kinase B (AURKB). [30], [48]
7-bromoindirubin-3-oxime [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for 7-bromoindirubin-3-oxime. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 7-bromoindirubin-3-oxime through regulating the expression of Aurora kinase B (AURKB). [30], [49]
7-fluoroindirubin-3-acetoxime [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for 7-fluoroindirubin-3-acetoxime. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 7-fluoroindirubin-3-acetoxime through regulating the expression of Aurora kinase B (AURKB). [30], [48]
CGP-57380 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for CGP-57380. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CGP-57380 through regulating the expression of Aurora kinase B (AURKB). [30], [50]
Deguelin [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for Deguelin. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Deguelin through regulating the expression of Aurora kinase B (AURKB). [30], [42]
HESPERADIN [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for HESPERADIN. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of HESPERADIN through regulating the expression of Aurora kinase B (AURKB). [30], [50]
Indirubin-3'-monoxime [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for Indirubin-3'-monoxime. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Indirubin-3'-monoxime through regulating the expression of Aurora kinase B (AURKB). [30], [48]
Indirubin-3-acetoxime [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for Indirubin-3-acetoxime. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Indirubin-3-acetoxime through regulating the expression of Aurora kinase B (AURKB). [30], [48]
Indirubin-3-methoxime [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for Indirubin-3-methoxime. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Indirubin-3-methoxime through regulating the expression of Aurora kinase B (AURKB). [30], [48]
ISIS 173813 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for ISIS 173813. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 173813 through regulating the expression of Aurora kinase B (AURKB). [30], [48]
ISIS 173831 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for ISIS 173831. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 173831 through regulating the expression of Aurora kinase B (AURKB). [30], [51]
ISIS 173840 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for ISIS 173840. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 173840 through regulating the expression of Aurora kinase B (AURKB). [30], [51]
ISIS 173848 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for ISIS 173848. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 173848 through regulating the expression of Aurora kinase B (AURKB). [30], [51]
quinazoline deriv. 1 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for quinazoline deriv. 1. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of quinazoline deriv. 1 through regulating the expression of Aurora kinase B (AURKB). [30], [52]
SU 6656 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for SU 6656. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of SU 6656 through regulating the expression of Aurora kinase B (AURKB). [30], [53]
PF-03814735 [Discontinued in Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Aurora kinase B (AURKB) is a therapeutic target for PF-03814735. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PF-03814735 through regulating the expression of Aurora kinase B (AURKB). [30], [54]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Recombinant human endostatin through regulating the expression of Beta-catenin (CTNNB1). [55], [56]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of C 82 through regulating the expression of Beta-catenin (CTNNB1). [55], [57]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CEQ-508 through regulating the expression of Beta-catenin (CTNNB1). [55], [58]
Bone morphogenetic protein 2 (BMP2)
DWP-431 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Bone morphogenetic protein 2 (BMP2) is a therapeutic target for DWP-431. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of DWP-431 through regulating the expression of Bone morphogenetic protein 2 (BMP2). [59], [60]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of STO609 through regulating the expression of Calmodulin-dependent kinase II (CAMKK2). [61], [62]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Contusugene ladenovec through regulating the expression of Cellular tumor antigen p53 (TP53). [63], [64]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of QPI-1002 through regulating the expression of Cellular tumor antigen p53 (TP53). [63], [65]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Thymoquinone through regulating the expression of Cellular tumor antigen p53 (TP53). [63], [66]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Ad-p53 through regulating the expression of Cellular tumor antigen p53 (TP53). [63], [67]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ALT-801 through regulating the expression of Cellular tumor antigen p53 (TP53). [63], [68]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of APG-115 through regulating the expression of Cellular tumor antigen p53 (TP53). [63], [69]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of APR-246 through regulating the expression of Cellular tumor antigen p53 (TP53). [63], [70]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Cenersen through regulating the expression of Cellular tumor antigen p53 (TP53). [63], [71]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of INGN-225 through regulating the expression of Cellular tumor antigen p53 (TP53). [15], [63]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISA-P53-01 through regulating the expression of Cellular tumor antigen p53 (TP53). [63], [72]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Kevetrin through regulating the expression of Cellular tumor antigen p53 (TP53). [13], [63]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of OPI-1002 through regulating the expression of Cellular tumor antigen p53 (TP53). [63], [73]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of SGT-53 through regulating the expression of Cellular tumor antigen p53 (TP53). [15], [63]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CGM097 through regulating the expression of Cellular tumor antigen p53 (TP53). [15], [63]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of COTI-2 through regulating the expression of Cellular tumor antigen p53 (TP53). [63], [74]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Dendritic cell vaccine through regulating the expression of Cellular tumor antigen p53 (TP53). [63], [75]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of HDM201 through regulating the expression of Cellular tumor antigen p53 (TP53). [63], [76]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ONYX-015 through regulating the expression of Cellular tumor antigen p53 (TP53). [63], [77]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of SAR-405838 through regulating the expression of Cellular tumor antigen p53 (TP53). [63], [64]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [63], [78]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AHL through regulating the expression of Cellular tumor antigen p53 (TP53). [63], [79]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NU-8231 through regulating the expression of Cellular tumor antigen p53 (TP53). [63], [80]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NUTLIN-3 through regulating the expression of Cellular tumor antigen p53 (TP53). [63], [81]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of INGN-234 through regulating the expression of Cellular tumor antigen p53 (TP53). [63], [82]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Pifithrin-alpha through regulating the expression of Cellular tumor antigen p53 (TP53). [63], [83]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of TAR-1 through regulating the expression of Cellular tumor antigen p53 (TP53). [63], [84]
Deubiquitinating enzyme 1 (USP1)
ML323 [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Deubiquitinating enzyme 1 (USP1) is a therapeutic target for ML323. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ML323 through regulating the expression of Deubiquitinating enzyme 1 (USP1). [85], [86]
DNA [cytosine-5]-methyltransferase 3B (DNMT3B)
Curcumin [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary DNA [cytosine-5]-methyltransferase 3B (DNMT3B) is a therapeutic target for Curcumin. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Curcumin through regulating the expression of DNA [cytosine-5]-methyltransferase 3B (DNMT3B). [87], [88]
(L-)-S-adenosyl-L-homocysteine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary DNA [cytosine-5]-methyltransferase 3B (DNMT3B) is a therapeutic target for (L-)-S-adenosyl-L-homocysteine. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of (L-)-S-adenosyl-L-homocysteine through regulating the expression of DNA [cytosine-5]-methyltransferase 3B (DNMT3B). [87], [89]
NSC-106084 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary DNA [cytosine-5]-methyltransferase 3B (DNMT3B) is a therapeutic target for NSC-106084. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NSC-106084 through regulating the expression of DNA [cytosine-5]-methyltransferase 3B (DNMT3B). [87], [89]
NSC-137546 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary DNA [cytosine-5]-methyltransferase 3B (DNMT3B) is a therapeutic target for NSC-137546. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NSC-137546 through regulating the expression of DNA [cytosine-5]-methyltransferase 3B (DNMT3B). [87], [89]
NSC-138419 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary DNA [cytosine-5]-methyltransferase 3B (DNMT3B) is a therapeutic target for NSC-138419. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NSC-138419 through regulating the expression of DNA [cytosine-5]-methyltransferase 3B (DNMT3B). [87], [89]
NSC-154957 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary DNA [cytosine-5]-methyltransferase 3B (DNMT3B) is a therapeutic target for NSC-154957. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NSC-154957 through regulating the expression of DNA [cytosine-5]-methyltransferase 3B (DNMT3B). [87], [89]
NSC-158324 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary DNA [cytosine-5]-methyltransferase 3B (DNMT3B) is a therapeutic target for NSC-158324. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NSC-158324 through regulating the expression of DNA [cytosine-5]-methyltransferase 3B (DNMT3B). [87], [89]
NSC-319745 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary DNA [cytosine-5]-methyltransferase 3B (DNMT3B) is a therapeutic target for NSC-319745. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NSC-319745 through regulating the expression of DNA [cytosine-5]-methyltransferase 3B (DNMT3B). [87], [89]
NSC-345763 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary DNA [cytosine-5]-methyltransferase 3B (DNMT3B) is a therapeutic target for NSC-345763. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NSC-345763 through regulating the expression of DNA [cytosine-5]-methyltransferase 3B (DNMT3B). [87], [89]
NSC-348926 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary DNA [cytosine-5]-methyltransferase 3B (DNMT3B) is a therapeutic target for NSC-348926. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NSC-348926 through regulating the expression of DNA [cytosine-5]-methyltransferase 3B (DNMT3B). [87], [89]
NSC-401077 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary DNA [cytosine-5]-methyltransferase 3B (DNMT3B) is a therapeutic target for NSC-401077. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NSC-401077 through regulating the expression of DNA [cytosine-5]-methyltransferase 3B (DNMT3B). [87], [89]
NSC-54162 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary DNA [cytosine-5]-methyltransferase 3B (DNMT3B) is a therapeutic target for NSC-54162. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NSC-54162 through regulating the expression of DNA [cytosine-5]-methyltransferase 3B (DNMT3B). [87], [89]
NSC-56071 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary DNA [cytosine-5]-methyltransferase 3B (DNMT3B) is a therapeutic target for NSC-56071. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NSC-56071 through regulating the expression of DNA [cytosine-5]-methyltransferase 3B (DNMT3B). [87], [89]
NSC-57893 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary DNA [cytosine-5]-methyltransferase 3B (DNMT3B) is a therapeutic target for NSC-57893. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NSC-57893 through regulating the expression of DNA [cytosine-5]-methyltransferase 3B (DNMT3B). [87], [89]
NSC-622444 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary DNA [cytosine-5]-methyltransferase 3B (DNMT3B) is a therapeutic target for NSC-622444. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NSC-622444 through regulating the expression of DNA [cytosine-5]-methyltransferase 3B (DNMT3B). [87], [89]
NSC-622445 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary DNA [cytosine-5]-methyltransferase 3B (DNMT3B) is a therapeutic target for NSC-622445. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NSC-622445 through regulating the expression of DNA [cytosine-5]-methyltransferase 3B (DNMT3B). [87], [90]
NSC-623548 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary DNA [cytosine-5]-methyltransferase 3B (DNMT3B) is a therapeutic target for NSC-623548. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NSC-623548 through regulating the expression of DNA [cytosine-5]-methyltransferase 3B (DNMT3B). [87], [89]
S-tubercidinylhomocysteine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary DNA [cytosine-5]-methyltransferase 3B (DNMT3B) is a therapeutic target for S-tubercidinylhomocysteine. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of S-tubercidinylhomocysteine through regulating the expression of DNA [cytosine-5]-methyltransferase 3B (DNMT3B). [87], [91]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BVD-523 through regulating the expression of Ephrin type-B receptor 2 (EPHB2). [92], [93]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of SEphB4-HSA through regulating the expression of Ephrin type-B receptor 2 (EPHB2). [92], [94]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of KO-947 through regulating the expression of Ephrin type-B receptor 2 (EPHB2). [15], [92]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of MK-8353 through regulating the expression of Ephrin type-B receptor 2 (EPHB2). [15], [92]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AMP-PNP through regulating the expression of Ephrin type-B receptor 2 (EPHB2). [92], [95]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of SNEWIQPRLPQH through regulating the expression of Ephrin type-B receptor 2 (EPHB2). [15], [92]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Afatinib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [31]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Cetuximab through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [96]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Dacomitinib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [97]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Epidermal growth factor through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [98]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of HEGF through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [99]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Icotinib hydrochloride through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [100]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Lapatinib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [101]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Merimepodib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [102]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Necitumumab through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [103]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NERATINIB MALEATE through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [104]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Nitroglycerin through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [102]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Panitumumab through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [105]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of SKI-758 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Vandetanib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [107]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AC0010 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [108]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Almonertinib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [109]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Amivantamab through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [110]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ASP1929 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [111]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CO-1686 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of DE-766 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [112]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of EGF816 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of HKI-272 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [113]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Indium-111 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [64]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Rindopepimut through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [114]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of SYM-004 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [115]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Varlitinib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [7]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Zalutumumab through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [97]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ABT-414 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [96]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ABX-EGF through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [116]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AFM24 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [117]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ASP8273 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [118]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BDTX-189 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [119]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BMS-599626 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [31]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BMS-690514 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [114]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CART-EGFR through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [120]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CetuGEX through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [121]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CI-1033 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [15]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CK-101 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [15]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Depatuxizumab through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [15]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of EGFR antisense DNA through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [15]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of EGFR CART through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [122]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of EMB-01 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [123]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of EMD 55900 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [124]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of HER1-VSSP vaccine through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [125]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of HM-78136B through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [126]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Matuzumab through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [127]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of MEHD-7945A through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [128]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Pelitinib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [129]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of RM-1929 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [130]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of SN-32793 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [131]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Sym013 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [132]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Sym015 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [122]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Tarloxotinib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [133]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of TT-100 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [134]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of VATALANIB through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [64]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ZN-e4 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [135]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AMG 595 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [136]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Anti-EGFR CAR T through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [137]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AP32788 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [138]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AST-1306 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [64]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BCA101 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [139]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BIBX-1382 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [140]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Cipatinib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [141]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CLN-081 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [142]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CUDC-101 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [143]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of D2C7 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [144]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of EGFR806-specific CAR T cell through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [145]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of IMGN289 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of JNJ-26483327 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [146]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of LY3164530 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [147]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of MCLA-158 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [148]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of MM-151 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [15]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of MR1-1 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [149]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PF-05230907 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [122]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Pyrotinib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [150]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of S-222611 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of SI-B001 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [151]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of SYN004 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [122]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 111In-hEGF through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [152]
(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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [153]
(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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of (3-Bromo-phenyl)-quinazolin-4-yl-amine through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [154]
(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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of (E)-5-(4-Hydroxybenzylidene)-1-phenethylhydantoin through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [155]
(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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [153]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 10-hydroxy-18-methoxybetaenone through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [153]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [156]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [157]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 2-benzoyl-3-(3,4-dihydroxyphenyl)acrylonitrile through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [153]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 2-cyano-3-(3,4-dihydroxyphenyl)acrylamide through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [153]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 2-methoxy-4-(2-nitrovinyl)phenol through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [153]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [158]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [159]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [160]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [161]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [162]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [163]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [153]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 4-(2-nitrovinyl)benzene-1,2-diol through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [164]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 4-(2-nitrovinyl)phenol through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [153]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [165]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [154]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 4-(4-(2-nitrovinyl)phenoxysulfonyl)benzoic acid through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [153]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [166]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 4-acrylamido-N-(3-bromophenyl)-2-hydroxybenzamide through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [167]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [168]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 4557W through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [169]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [170]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 5-acrylamido-N-(3-bromophenyl)-2-hydroxybenzamide through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [171]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [168]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [168]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 6,7-diethoxy-4-styrylquinazoline through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [168]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 6,7-dimethoxy-4-(2-phenylethynyl)quinazoline through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [168]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [168]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [172]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [161]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [161]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AFM-21 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AG 112 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [173]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AG 9 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AG-213 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [153]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AG-538 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [174]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AG1478 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [175]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AGT-2000 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AL-6802 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Anti-EGFR humanized mabs through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Anti-EGFR mab through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ARX-AHD through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [165]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Benzyl-quinazolin-4-yl-amine through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [166]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Bmab-200 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BPIQ-I through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [176]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CL-387785 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [167]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Cochliobolic acid through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [177]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of EDP-13 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of EGFR inhibitor through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [178]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Epitinib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of FHT-2107 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of GI-3000 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of HDS-029 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [179]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of HKI-9924129 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [180]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of HM-61713B through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of HTS-00213 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [161]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of HTS-02876 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [181]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of HTS-05058 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [158]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ICR 62 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [182]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of IPS-01003 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of LA22-radioimmunoconjugates through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of LAVENDUSTIN A through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [168]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of mabionHER2 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of MDP-01 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of MG-111 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [183]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of MT-062 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [184]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [185]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [186]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [174]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of N-(4-(phenylamino)quinazolin-6-yl)acrylamide through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [182]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [156]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [1], [154]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of N4-(3-chlorophenyl)quinazoline-4,6-diamine through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [184]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of N4-(3-methylphenyl)-4,6-quinazolinediamine through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [158]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NRC-2694 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ON-128 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [154]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of OSI-75 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [187]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PD-0166326 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [155]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PD-0173956 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [155]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PD-158780 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [154]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PD-168393 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [186]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PD182905 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [131]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PF 5208766 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [188]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PP121 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [189]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of RG-50810 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [181]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of RM-6427 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Ro-4396686 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [158]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of RX-1792 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of SYM-011 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of TGF alpha through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Theliatinib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [190]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of WHI-P154 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [172]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of WZ-3146 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AZD-9935 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [191]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AZD4769 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [31]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CGP-52411 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [192]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CGP-53353 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [131]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Heparin-EGF-like factor through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [193]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PD-153035 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [194]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PKI166 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [195]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of RG7160 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [196]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of TAK165 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [197]
Forkhead box protein M1 (FOXM1)
(D-Arg)(9)-p19(ARF) 26-44 peptide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Forkhead box protein M1 (FOXM1) is a therapeutic target for (D-Arg)(9)-p19(ARF) 26-44 peptide. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of (D-Arg)(9)-p19(ARF) 26-44 peptide through regulating the expression of Forkhead box protein M1 (FOXM1). [198], [199]
Frizzled-10 (FZD10)
OTSA-101-DTPA-90Y [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Frizzled-10 (FZD10) is a therapeutic target for OTSA-101-DTPA-90Y. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of OTSA-101-DTPA-90Y through regulating the expression of Frizzled-10 (FZD10). [64], [200]
High mobility group protein B1 (HMGB1)
2-Sulfhydryl-Ethanol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary High mobility group protein B1 (HMGB1) is a therapeutic target for 2-Sulfhydryl-Ethanol. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 2-Sulfhydryl-Ethanol through regulating the expression of High mobility group protein B1 (HMGB1). [201], [202]
Hypoxia-inducible factor 1 alpha (HIF-1A)
HIF-1alpha [Phase 4]
In total 1 mechanisms lead to this potential drug response
Response Summary Hypoxia-inducible factor 1 alpha (HIF-1A) is a therapeutic target for HIF-1alpha. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of HIF-1alpha through regulating the expression of Hypoxia-inducible factor 1 alpha (HIF-1A). [203], [204]
IT-101 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Hypoxia-inducible factor 1 alpha (HIF-1A) is a therapeutic target for IT-101. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of IT-101 through regulating the expression of Hypoxia-inducible factor 1 alpha (HIF-1A). [203], [205]
2-Methoxyestradiol [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Hypoxia-inducible factor 1 alpha (HIF-1A) is a therapeutic target for 2-Methoxyestradiol. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 2-Methoxyestradiol through regulating the expression of Hypoxia-inducible factor 1 alpha (HIF-1A). [203], [206]
PT2385 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Hypoxia-inducible factor 1 alpha (HIF-1A) is a therapeutic target for PT2385. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PT2385 through regulating the expression of Hypoxia-inducible factor 1 alpha (HIF-1A). [203], [207]
ENMD-1198 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Hypoxia-inducible factor 1 alpha (HIF-1A) is a therapeutic target for ENMD-1198. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ENMD-1198 through regulating the expression of Hypoxia-inducible factor 1 alpha (HIF-1A). [203], [208]
EZN-2968 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Hypoxia-inducible factor 1 alpha (HIF-1A) is a therapeutic target for EZN-2968. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of EZN-2968 through regulating the expression of Hypoxia-inducible factor 1 alpha (HIF-1A). [203], [209]
PX-478 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Hypoxia-inducible factor 1 alpha (HIF-1A) is a therapeutic target for PX-478. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PX-478 through regulating the expression of Hypoxia-inducible factor 1 alpha (HIF-1A). [203], [210]
(5-(1-benzyl-1H-indazol-3-yl)furan-2-yl)methanol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Hypoxia-inducible factor 1 alpha (HIF-1A) is a therapeutic target for (5-(1-benzyl-1H-indazol-3-yl)furan-2-yl)methanol. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of (5-(1-benzyl-1H-indazol-3-yl)furan-2-yl)methanol through regulating the expression of Hypoxia-inducible factor 1 alpha (HIF-1A). [15], [203]
ISIS 175510 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Hypoxia-inducible factor 1 alpha (HIF-1A) is a therapeutic target for ISIS 175510. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 175510 through regulating the expression of Hypoxia-inducible factor 1 alpha (HIF-1A). [203], [211]
ISIS 298697 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Hypoxia-inducible factor 1 alpha (HIF-1A) is a therapeutic target for ISIS 298697. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 298697 through regulating the expression of Hypoxia-inducible factor 1 alpha (HIF-1A). [203], [211]
ISIS 298699 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Hypoxia-inducible factor 1 alpha (HIF-1A) is a therapeutic target for ISIS 298699. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 298699 through regulating the expression of Hypoxia-inducible factor 1 alpha (HIF-1A). [203], [211]
ISIS 298700 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Hypoxia-inducible factor 1 alpha (HIF-1A) is a therapeutic target for ISIS 298700. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 298700 through regulating the expression of Hypoxia-inducible factor 1 alpha (HIF-1A). [203], [211]
ISIS 298701 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Hypoxia-inducible factor 1 alpha (HIF-1A) is a therapeutic target for ISIS 298701. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 298701 through regulating the expression of Hypoxia-inducible factor 1 alpha (HIF-1A). [203], [211]
ISIS 298702 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Hypoxia-inducible factor 1 alpha (HIF-1A) is a therapeutic target for ISIS 298702. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 298702 through regulating the expression of Hypoxia-inducible factor 1 alpha (HIF-1A). [203], [211]
ISIS 298711 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Hypoxia-inducible factor 1 alpha (HIF-1A) is a therapeutic target for ISIS 298711. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 298711 through regulating the expression of Hypoxia-inducible factor 1 alpha (HIF-1A). [203], [211]
ISIS 298712 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Hypoxia-inducible factor 1 alpha (HIF-1A) is a therapeutic target for ISIS 298712. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 298712 through regulating the expression of Hypoxia-inducible factor 1 alpha (HIF-1A). [203], [211]
ISIS 298743 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Hypoxia-inducible factor 1 alpha (HIF-1A) is a therapeutic target for ISIS 298743. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 298743 through regulating the expression of Hypoxia-inducible factor 1 alpha (HIF-1A). [203], [211]
ISIS 298744 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Hypoxia-inducible factor 1 alpha (HIF-1A) is a therapeutic target for ISIS 298744. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 298744 through regulating the expression of Hypoxia-inducible factor 1 alpha (HIF-1A). [203], [211]
ISIS 298745 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Hypoxia-inducible factor 1 alpha (HIF-1A) is a therapeutic target for ISIS 298745. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 298745 through regulating the expression of Hypoxia-inducible factor 1 alpha (HIF-1A). [203], [211]
ISIS 298746 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Hypoxia-inducible factor 1 alpha (HIF-1A) is a therapeutic target for ISIS 298746. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 298746 through regulating the expression of Hypoxia-inducible factor 1 alpha (HIF-1A). [203], [212]
Insulin-like growth factor I receptor (IGF1R)
Mecasermin [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for Mecasermin. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Mecasermin through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [214]
Somatomedin-1 [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for Somatomedin-1. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Somatomedin-1 through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [15], [213]
Teprotumumab [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for Teprotumumab. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Teprotumumab through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [215]
Rinfabate [Phase 2/3]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for Rinfabate. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Rinfabate through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [216]
AMG 479 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for AMG 479. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AMG 479 through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [7], [213]
AXL-1717 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for AXL-1717. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AXL-1717 through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [125], [213]
Cixutumumab [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for Cixutumumab. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Cixutumumab through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [217]
MM-141 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for MM-141. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of MM-141 through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [218]
R1507 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for R1507. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of R1507 through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [219]
TT-100 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for TT-100. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of TT-100 through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [220]
VPI-2690B [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for VPI-2690B. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of VPI-2690B through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [221]
AEW-541 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for AEW-541. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AEW-541 through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [222]
BIIB 022 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for BIIB 022. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BIIB 022 through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [223]
Cyclolignan picropodophyllin [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for Cyclolignan picropodophyllin. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Cyclolignan picropodophyllin through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [31], [213]
FPI-1434 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for FPI-1434. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of FPI-1434 through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [224]
HF-0299 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for HF-0299. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of HF-0299 through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [225]
RG-7010 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for RG-7010. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of RG-7010 through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [226]
ATL-1101 [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for ATL-1101. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ATL-1101 through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [89], [213]
BMS-695735 [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for BMS-695735. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BMS-695735 through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [152], [213]
4-((1H-indazol-6-ylamino)methyl)benzene-1,2-diol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for 4-((1H-indazol-6-ylamino)methyl)benzene-1,2-diol. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 4-((1H-indazol-6-ylamino)methyl)benzene-1,2-diol through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [227]
4-((naphthalen-2-ylamino)methyl)benzene-1,2-diol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for 4-((naphthalen-2-ylamino)methyl)benzene-1,2-diol. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 4-((naphthalen-2-ylamino)methyl)benzene-1,2-diol through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [228]
AG 1024 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for AG 1024. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AG 1024 through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [229]
Alpha-D-Mannose [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for Alpha-D-Mannose. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Alpha-D-Mannose through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [230]
AMP-PNP [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for AMP-PNP. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AMP-PNP through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [230]
AZD3463 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for AZD3463. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AZD3463 through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [231]
BMS 536924 [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for BMS 536924. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BMS 536924 through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [227]
Fucose [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for Fucose. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Fucose through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [4], [213]
GSK-1838705A [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for GSK-1838705A. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of GSK-1838705A through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [232]
GSK1511931 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for GSK1511931. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of GSK1511931 through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [233]
JB-1 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for JB-1. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of JB-1 through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [234]
NVP-ADW742 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for NVP-ADW742. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NVP-ADW742 through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [4], [213]
PQ401 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for PQ401. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PQ401 through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [235]
AVE-1642 [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for AVE-1642. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AVE-1642 through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [236]
Figitumumab [Discontinued in Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for Figitumumab. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Figitumumab through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [64], [213]
KW-2450 [Discontinued in Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Insulin-like growth factor I receptor (IGF1R) is a therapeutic target for KW-2450. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of KW-2450 through regulating the expression of Insulin-like growth factor I receptor (IGF1R). [213], [237]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Interferon beta-1a through regulating the expression of Interferon-beta (IFNB1). [238], [239]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PEGylated IFN beta 1-a through regulating the expression of Interferon-beta (IFNB1). [238], [240]
PLEGRIDY [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Interferon-beta (IFNB1) is a therapeutic target for PLEGRIDY. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PLEGRIDY through regulating the expression of Interferon-beta (IFNB1). [238], [241]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Biferonex through regulating the expression of Interferon-beta (IFNB1). [238], [242]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of FP-1201 through regulating the expression of Interferon-beta (IFNB1). [238], [243]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NU-100 through regulating the expression of Interferon-beta (IFNB1). [238], [244]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AZ-01, PEGylated interferon-beta through regulating the expression of Interferon-beta (IFNB1). [64], [238]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Interferon beta 1a through regulating the expression of Interferon-beta (IFNB1). [238], [245]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PF-06823859 through regulating the expression of Interferon-beta (IFNB1). [238], [245]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ARX-424 through regulating the expression of Interferon-beta (IFNB1). [238], [246]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Gene therapy, IFN-b through regulating the expression of Interferon-beta (IFNB1). [238], [247]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of TV-1390 through regulating the expression of Interferon-beta (IFNB1). [238], [245]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Maxy-10 through regulating the expression of Interferon-beta (IFNB1). [238], [248]
Janus kinase 2 (JAK-2)
Baricitinib [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for Baricitinib. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Baricitinib through regulating the expression of Janus kinase 2 (JAK-2). [249], [250]
Fedratinib [Approved]
In total 2 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for Fedratinib. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Fedratinib through regulating the expression of Janus kinase 2 (JAK-2). [249], [251]
Janus kinase 2 (JAK-2) is a therapeutic target for Fedratinib. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Fedratinib through regulating the expression of Janus kinase 2 (JAK-2). [249], [269]
Ruxolitinib [Approved]
In total 2 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for Ruxolitinib. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Ruxolitinib through regulating the expression of Janus kinase 2 (JAK-2). [249], [252]
Janus kinase 2 (JAK-2) is a therapeutic target for Ruxolitinib. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Ruxolitinib through regulating the expression of Janus kinase 2 (JAK-2). [58], [249]
CYT-387 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for CYT-387. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CYT-387 through regulating the expression of Janus kinase 2 (JAK-2). [249], [253]
ITF2357 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for ITF2357. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ITF2357 through regulating the expression of Janus kinase 2 (JAK-2). [249], [254]
Pacritinib [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for Pacritinib. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Pacritinib through regulating the expression of Janus kinase 2 (JAK-2). [249], [255]
XL019 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for XL019. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of XL019 through regulating the expression of Janus kinase 2 (JAK-2). [249], [256]
AZD1480 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for AZD1480. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AZD1480 through regulating the expression of Janus kinase 2 (JAK-2). [249], [257]
BMS-911543 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for BMS-911543. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BMS-911543 through regulating the expression of Janus kinase 2 (JAK-2). [249], [258]
Cerdulatinib [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for Cerdulatinib. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Cerdulatinib through regulating the expression of Janus kinase 2 (JAK-2). [249], [259]
CTP-543 [Phase 2]
In total 2 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for CTP-543. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CTP-543 through regulating the expression of Janus kinase 2 (JAK-2). [249], [260]
Janus kinase 2 (JAK-2) is a therapeutic target for CTP-543. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CTP-543 through regulating the expression of Janus kinase 2 (JAK-2). [249], [256]
INCB039110 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for INCB039110. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of INCB039110 through regulating the expression of Janus kinase 2 (JAK-2). [249], [261]
LY2784544 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for LY2784544. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of LY2784544 through regulating the expression of Janus kinase 2 (JAK-2). [249], [262]
NS-018 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for NS-018. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NS-018 through regulating the expression of Janus kinase 2 (JAK-2). [249], [260]
AC430 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for AC430. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AC430 through regulating the expression of Janus kinase 2 (JAK-2). [249], [263]
Peginterferon beta [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for Peginterferon beta. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Peginterferon beta through regulating the expression of Janus kinase 2 (JAK-2). [249], [252]
SB-1578 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for SB-1578. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of SB-1578 through regulating the expression of Janus kinase 2 (JAK-2). [249], [264]
1,2,3,4,5,6-hexabromocyclohexane [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for 1,2,3,4,5,6-hexabromocyclohexane. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 1,2,3,4,5,6-hexabromocyclohexane through regulating the expression of Janus kinase 2 (JAK-2). [249], [265]
5-phenyl-1H-indazol-3-amine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for 5-phenyl-1H-indazol-3-amine. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 5-phenyl-1H-indazol-3-amine through regulating the expression of Janus kinase 2 (JAK-2). [249], [266]
AMG-JAK2-01 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for AMG-JAK2-01. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AMG-JAK2-01 through regulating the expression of Janus kinase 2 (JAK-2). [249], [260]
Atropisomer 1 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for Atropisomer 1. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Atropisomer 1 through regulating the expression of Janus kinase 2 (JAK-2). [249], [267]
AZ960 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for AZ960. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AZ960 through regulating the expression of Janus kinase 2 (JAK-2). [70], [249]
BVB-808 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for BVB-808. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BVB-808 through regulating the expression of Janus kinase 2 (JAK-2). [249], [268]
CMP-6 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for CMP-6. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CMP-6 through regulating the expression of Janus kinase 2 (JAK-2). [190], [249]
K-454 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for K-454. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of K-454 through regulating the expression of Janus kinase 2 (JAK-2). [249], [270]
NSC-1771 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for NSC-1771. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NSC-1771 through regulating the expression of Janus kinase 2 (JAK-2). [249], [271]
ON-044580 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for ON-044580. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ON-044580 through regulating the expression of Janus kinase 2 (JAK-2). [249], [260]
SGI-1252 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for SGI-1252. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of SGI-1252 through regulating the expression of Janus kinase 2 (JAK-2). [249], [272]
WHI-P154 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for WHI-P154. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of WHI-P154 through regulating the expression of Janus kinase 2 (JAK-2). [249], [273]
AG490 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Janus kinase 2 (JAK-2) is a therapeutic target for AG490. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AG490 through regulating the expression of Janus kinase 2 (JAK-2). [249], [252]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of APTO-253 through regulating the expression of Kruppel like factor 4 (KLF4). [73], [274]
MADH6 messenger RNA (MADH6 mRNA)
ISIS 101952 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary MADH6 messenger RNA (MADH6 mRNA) is a therapeutic target for ISIS 101952. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 101952 through regulating the expression of MADH6 messenger RNA (MADH6 mRNA). [275], [276]
ISIS 101960 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary MADH6 messenger RNA (MADH6 mRNA) is a therapeutic target for ISIS 101960. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 101960 through regulating the expression of MADH6 messenger RNA (MADH6 mRNA). [275], [276]
ISIS 101983 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary MADH6 messenger RNA (MADH6 mRNA) is a therapeutic target for ISIS 101983. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 101983 through regulating the expression of MADH6 messenger RNA (MADH6 mRNA). [275], [276]
ISIS 101984 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary MADH6 messenger RNA (MADH6 mRNA) is a therapeutic target for ISIS 101984. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 101984 through regulating the expression of MADH6 messenger RNA (MADH6 mRNA). [275], [276]
ISIS 101985 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary MADH6 messenger RNA (MADH6 mRNA) is a therapeutic target for ISIS 101985. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 101985 through regulating the expression of MADH6 messenger RNA (MADH6 mRNA). [275], [276]
ISIS 101986 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary MADH6 messenger RNA (MADH6 mRNA) is a therapeutic target for ISIS 101986. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 101986 through regulating the expression of MADH6 messenger RNA (MADH6 mRNA). [275], [276]
ISIS 101987 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary MADH6 messenger RNA (MADH6 mRNA) is a therapeutic target for ISIS 101987. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 101987 through regulating the expression of MADH6 messenger RNA (MADH6 mRNA). [275], [276]
ISIS 101995 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary MADH6 messenger RNA (MADH6 mRNA) is a therapeutic target for ISIS 101995. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 101995 through regulating the expression of MADH6 messenger RNA (MADH6 mRNA). [275], [276]
ISIS 101996 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary MADH6 messenger RNA (MADH6 mRNA) is a therapeutic target for ISIS 101996. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 101996 through regulating the expression of MADH6 messenger RNA (MADH6 mRNA). [275], [276]
ISIS 101997 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary MADH6 messenger RNA (MADH6 mRNA) is a therapeutic target for ISIS 101997. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 101997 through regulating the expression of MADH6 messenger RNA (MADH6 mRNA). [275], [276]
ISIS 101998 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary MADH6 messenger RNA (MADH6 mRNA) is a therapeutic target for ISIS 101998. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 101998 through regulating the expression of MADH6 messenger RNA (MADH6 mRNA). [275], [277]
Mothers against decapentaplegic homolog 3 (SMAD3)
FLUORESCEIN [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Mothers against decapentaplegic homolog 3 (SMAD3) is a therapeutic target for FLUORESCEIN. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of FLUORESCEIN through regulating the expression of Mothers against decapentaplegic homolog 3 (SMAD3). [275], [278]
SIS-3 [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Mothers against decapentaplegic homolog 3 (SMAD3) is a therapeutic target for SIS-3. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of SIS-3 through regulating the expression of Mothers against decapentaplegic homolog 3 (SMAD3). [267], [275]
ELLAGIC ACID [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Mothers against decapentaplegic homolog 3 (SMAD3) is a therapeutic target for ELLAGIC ACID. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ELLAGIC ACID through regulating the expression of Mothers against decapentaplegic homolog 3 (SMAD3). [267], [275]
GNF-PF-2272 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Mothers against decapentaplegic homolog 3 (SMAD3) is a therapeutic target for GNF-PF-2272. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of GNF-PF-2272 through regulating the expression of Mothers against decapentaplegic homolog 3 (SMAD3). [275], [279]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Alpelisib through regulating the expression of PI3-kinase alpha (PIK3CA). [1], [107]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BAY 80-6946 through regulating the expression of PI3-kinase alpha (PIK3CA). [1], [204]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Buparlisib through regulating the expression of PI3-kinase alpha (PIK3CA). [1], [280]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of GDC-0032 through regulating the expression of PI3-kinase alpha (PIK3CA). [1], [281]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of LY3023414 through regulating the expression of PI3-kinase alpha (PIK3CA). [1], [282]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of MLN1117 through regulating the expression of PI3-kinase alpha (PIK3CA). [1], [283]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PA-799 through regulating the expression of PI3-kinase alpha (PIK3CA). [1], [284]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BLY719 through regulating the expression of PI3-kinase alpha (PIK3CA). [1], [64]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of HHCYH33 through regulating the expression of PI3-kinase alpha (PIK3CA). [1], [285]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PWT-33597 through regulating the expression of PI3-kinase alpha (PIK3CA). [1], [286]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ETP-46321 through regulating the expression of PI3-kinase alpha (PIK3CA). [1], [287]
Programmed cell death 1 ligand 1 (PD-L1)
Atezolizumab [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for Atezolizumab. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Atezolizumab through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [289]
Avelumab [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for Avelumab. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Avelumab through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [241], [288]
Bavencio [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for Bavencio. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Bavencio through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [290]
Durvalumab [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for Durvalumab. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Durvalumab through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [291]
RG-7446 [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for RG-7446. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of RG-7446 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [292]
CS1001 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for CS1001. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CS1001 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [293]
KN046 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for KN046. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of KN046 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [294]
MEDI4736 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for MEDI4736. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of MEDI4736 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [295]
MPDL-3280A [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for MPDL-3280A. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of MPDL-3280A through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [296]
BGB-A333 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for BGB-A333. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BGB-A333 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [297]
Bintrafusp alfa [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for Bintrafusp alfa. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Bintrafusp alfa through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [298]
CX-072 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for CX-072. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CX-072 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [299]
GS-4224 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for GS-4224. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of GS-4224 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [300]
INCB86550 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for INCB86550. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of INCB86550 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [301]
KN035 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for KN035. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of KN035 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [302]
M7824 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for M7824. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of M7824 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [122], [288]
NM21-1480 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for NM21-1480. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NM21-1480 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [291]
Pidilizumab [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for Pidilizumab. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Pidilizumab through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [15], [288]
ALPN-202 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for ALPN-202. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ALPN-202 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [303]
Anti-PD-L1 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for Anti-PD-L1. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Anti-PD-L1 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [304]
Anti-PD-L1 CSR T cells [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for Anti-PD-L1 CSR T cells. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Anti-PD-L1 CSR T cells through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [15], [288]
BMS-986189 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for BMS-986189. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BMS-986189 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [291]
CA-170 [Phase 1]
In total 2 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for CA-170. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CA-170 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [122], [288]
Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for CA-170. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CA-170 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [305]
Cosibelimab [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for Cosibelimab. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Cosibelimab through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [306]
FAZ053 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for FAZ053. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of FAZ053 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [291]
FS118 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for FS118. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of FS118 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [307]
GEN1046 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for GEN1046. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of GEN1046 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [308]
IBI318 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for IBI318. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of IBI318 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [309]
INBRX-105 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for INBRX-105. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of INBRX-105 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [310]
KD033 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for KD033. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of KD033 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [311]
LY3300054 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for LY3300054. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of LY3300054 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [15], [288]
LY3415244 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for LY3415244. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of LY3415244 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [312]
MCLA-145 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for MCLA-145. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of MCLA-145 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [313]
MSB2311 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for MSB2311. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of MSB2311 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [291]
PD-L1 t-haNK [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for PD-L1 t-haNK. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PD-L1 t-haNK through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [314]
RG6084 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for RG6084. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of RG6084 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [122], [288]
TAK-252 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for TAK-252. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of TAK-252 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [315]
CA-327 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Programmed cell death 1 ligand 1 (PD-L1) is a therapeutic target for CA-327. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CA-327 through regulating the expression of Programmed cell death 1 ligand 1 (PD-L1). [288], [291]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of VP-102 through regulating the expression of Protein phosphatase 1A (PPM1A). [61], [316]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AZD5363 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [15], [317]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Enzastaurin through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [317], [318]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of GDC-0068 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [15], [317]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ARQ 092 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [317], [319]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CI-1033 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [15], [317]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CMX-2043 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [31], [317]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of GSK2110183 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [317], [320]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PTX-200 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [15], [317]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of RX-0201 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [317], [321]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Triciribine prodrug through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [145], [317]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ARQ 751 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [317], [321]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BMS-754807 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [317], [322]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of M2698 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [15], [317]
(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 RNA demethylase ALKBH5 (ALKBH5) 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). [317], [323]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [317], [324]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [317], [323]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of A-443654 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [317], [323]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of A-674563 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [317], [325]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Akt inhibitor VIII through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [230], [317]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ALM-301 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [233], [317]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Bisindolylmaleimide-I through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [317], [326]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BMS 536924 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [317], [323]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BX-517 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [317], [327]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CI-1040 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [317], [321]
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 RNA demethylase ALKBH5 (ALKBH5) 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). [317], [328]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of KN-62 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [317], [326]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Lactoquinomycin through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [317], [329]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of LD-101 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [317], [321]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of MYRIOCIN through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [317], [330]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NU-1001-41 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [317], [321]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of RO-316233 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [317], [323]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Ro31-8220 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [317], [331]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of SB-747651A through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [317], [332]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of STAUROSPORINONE through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [317], [330]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of VLI-27 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [317], [321]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Squalestatin 1 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [15], [317]
Signal transducer and activator of transcription 3 (STAT3)
Acitretin [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 3 (STAT3) is a therapeutic target for Acitretin. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Acitretin through regulating the expression of Signal transducer and activator of transcription 3 (STAT3). [333], [334]
Napabucasin [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 3 (STAT3) is a therapeutic target for Napabucasin. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Napabucasin through regulating the expression of Signal transducer and activator of transcription 3 (STAT3). [333], [335]
Atiprimod [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 3 (STAT3) is a therapeutic target for Atiprimod. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Atiprimod through regulating the expression of Signal transducer and activator of transcription 3 (STAT3). [333], [336]
GLG-801 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 3 (STAT3) is a therapeutic target for GLG-801. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of GLG-801 through regulating the expression of Signal transducer and activator of transcription 3 (STAT3). [333], [337]
Golotimod [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 3 (STAT3) is a therapeutic target for Golotimod. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Golotimod through regulating the expression of Signal transducer and activator of transcription 3 (STAT3). [15], [333]
IMX-110 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 3 (STAT3) is a therapeutic target for IMX-110. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of IMX-110 through regulating the expression of Signal transducer and activator of transcription 3 (STAT3). [15], [333]
ISIS-STAT3 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 3 (STAT3) is a therapeutic target for ISIS-STAT3. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS-STAT3 through regulating the expression of Signal transducer and activator of transcription 3 (STAT3). [333], [338]
NT219 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 3 (STAT3) is a therapeutic target for NT219. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NT219 through regulating the expression of Signal transducer and activator of transcription 3 (STAT3). [333], [339]
OPB-31121 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 3 (STAT3) is a therapeutic target for OPB-31121. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of OPB-31121 through regulating the expression of Signal transducer and activator of transcription 3 (STAT3). [15], [333]
WP-1066 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 3 (STAT3) is a therapeutic target for WP-1066. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of WP-1066 through regulating the expression of Signal transducer and activator of transcription 3 (STAT3). [15], [333]
C188-9 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 3 (STAT3) is a therapeutic target for C188-9. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of C188-9 through regulating the expression of Signal transducer and activator of transcription 3 (STAT3). [333], [340]
DSP-0337 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 3 (STAT3) is a therapeutic target for DSP-0337. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of DSP-0337 through regulating the expression of Signal transducer and activator of transcription 3 (STAT3). [4], [333]
OPB-111077 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 3 (STAT3) is a therapeutic target for OPB-111077. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of OPB-111077 through regulating the expression of Signal transducer and activator of transcription 3 (STAT3). [333], [341]
OPB-51602 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 3 (STAT3) is a therapeutic target for OPB-51602. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of OPB-51602 through regulating the expression of Signal transducer and activator of transcription 3 (STAT3). [333], [342]
TAK-114 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 3 (STAT3) is a therapeutic target for TAK-114. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of TAK-114 through regulating the expression of Signal transducer and activator of transcription 3 (STAT3). [333], [343]
WP1220 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 3 (STAT3) is a therapeutic target for WP1220. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of WP1220 through regulating the expression of Signal transducer and activator of transcription 3 (STAT3). [333], [344]
GNF-PF-1399 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 3 (STAT3) is a therapeutic target for GNF-PF-1399. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of GNF-PF-1399 through regulating the expression of Signal transducer and activator of transcription 3 (STAT3). [333], [345]
ISIS 113176 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 3 (STAT3) is a therapeutic target for ISIS 113176. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 113176 through regulating the expression of Signal transducer and activator of transcription 3 (STAT3). [333], [338]
ISIS 113187 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 3 (STAT3) is a therapeutic target for ISIS 113187. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 113187 through regulating the expression of Signal transducer and activator of transcription 3 (STAT3). [333], [338]
ISIS 113209 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 3 (STAT3) is a therapeutic target for ISIS 113209. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 113209 through regulating the expression of Signal transducer and activator of transcription 3 (STAT3). [333], [338]
ISIS 113210 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 3 (STAT3) is a therapeutic target for ISIS 113210. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 113210 through regulating the expression of Signal transducer and activator of transcription 3 (STAT3). [15], [333]
ISIS 17148 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 3 (STAT3) is a therapeutic target for ISIS 17148. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 17148 through regulating the expression of Signal transducer and activator of transcription 3 (STAT3). [333], [338]
ISIS 17152 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Signal transducer and activator of transcription 3 (STAT3) is a therapeutic target for ISIS 17152. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ISIS 17152 through regulating the expression of Signal transducer and activator of transcription 3 (STAT3). [333], [338]
Sphingosine kinase 1 (SPHK1)
Phenoxodiol [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Sphingosine kinase 1 (SPHK1) is a therapeutic target for Phenoxodiol. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Phenoxodiol through regulating the expression of Sphingosine kinase 1 (SPHK1). [346], [347]
GSK618334 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Sphingosine kinase 1 (SPHK1) is a therapeutic target for GSK618334. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of GSK618334 through regulating the expression of Sphingosine kinase 1 (SPHK1). [64], [346]
YP-005 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Sphingosine kinase 1 (SPHK1) is a therapeutic target for YP-005. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of YP-005 through regulating the expression of Sphingosine kinase 1 (SPHK1). [346], [348]
PF-543 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Sphingosine kinase 1 (SPHK1) is a therapeutic target for PF-543. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PF-543 through regulating the expression of Sphingosine kinase 1 (SPHK1). [346], [349]
SK1-I [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Sphingosine kinase 1 (SPHK1) is a therapeutic target for SK1-I. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of SK1-I through regulating the expression of Sphingosine kinase 1 (SPHK1). [346], [350]
VPC-94075 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Sphingosine kinase 1 (SPHK1) is a therapeutic target for VPC-94075. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of VPC-94075 through regulating the expression of Sphingosine kinase 1 (SPHK1). [346], [351]
B-5354a [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Sphingosine kinase 1 (SPHK1) is a therapeutic target for B-5354a. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of B-5354a through regulating the expression of Sphingosine kinase 1 (SPHK1). [346], [352]
F-12509A [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Sphingosine kinase 1 (SPHK1) is a therapeutic target for F-12509A. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of F-12509A through regulating the expression of Sphingosine kinase 1 (SPHK1). [346], [353]
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 RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of SPHINX31 through regulating the expression of SRSF protein kinase 1 (SRPK1). [354], [355]
Stimulator of interferon genes protein (TMEM173)
ADU- S100 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Stimulator of interferon genes protein (TMEM173) is a therapeutic target for ADU- S100. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ADU- S100 through regulating the expression of Stimulator of interferon genes protein (TMEM173). [201], [356]
ADU-S100 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Stimulator of interferon genes protein (TMEM173) is a therapeutic target for ADU-S100. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ADU-S100 through regulating the expression of Stimulator of interferon genes protein (TMEM173). [201], [357]
IMSA101 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Stimulator of interferon genes protein (TMEM173) is a therapeutic target for IMSA101. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of IMSA101 through regulating the expression of Stimulator of interferon genes protein (TMEM173). [15], [201]
MK-1454 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Stimulator of interferon genes protein (TMEM173) is a therapeutic target for MK-1454. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of MK-1454 through regulating the expression of Stimulator of interferon genes protein (TMEM173). [201], [358]
BMS-986301 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Stimulator of interferon genes protein (TMEM173) is a therapeutic target for BMS-986301. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BMS-986301 through regulating the expression of Stimulator of interferon genes protein (TMEM173). [201], [359]
E7766 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Stimulator of interferon genes protein (TMEM173) is a therapeutic target for E7766. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of E7766 through regulating the expression of Stimulator of interferon genes protein (TMEM173). [201], [360]
GSK3745417 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Stimulator of interferon genes protein (TMEM173) is a therapeutic target for GSK3745417. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of GSK3745417 through regulating the expression of Stimulator of interferon genes protein (TMEM173). [201], [361]
MK-2118 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Stimulator of interferon genes protein (TMEM173) is a therapeutic target for MK-2118. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of MK-2118 through regulating the expression of Stimulator of interferon genes protein (TMEM173). [201], [362]
SB 11285 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Stimulator of interferon genes protein (TMEM173) is a therapeutic target for SB 11285. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of SB 11285 through regulating the expression of Stimulator of interferon genes protein (TMEM173). [201], [363]
SNX281 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Stimulator of interferon genes protein (TMEM173) is a therapeutic target for SNX281. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of SNX281 through regulating the expression of Stimulator of interferon genes protein (TMEM173). [201], [364]
SYNB1891 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Stimulator of interferon genes protein (TMEM173) is a therapeutic target for SYNB1891. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of SYNB1891 through regulating the expression of Stimulator of interferon genes protein (TMEM173). [201], [365]
TAK-676 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Stimulator of interferon genes protein (TMEM173) is a therapeutic target for TAK-676. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of TAK-676 through regulating the expression of Stimulator of interferon genes protein (TMEM173). [201], [366]
C-176 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stimulator of interferon genes protein (TMEM173) is a therapeutic target for C-176. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of C-176 through regulating the expression of Stimulator of interferon genes protein (TMEM173). [201], [367]
C-178 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stimulator of interferon genes protein (TMEM173) is a therapeutic target for C-178. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of C-178 through regulating the expression of Stimulator of interferon genes protein (TMEM173). [201], [368]
Stress-activated protein kinase JNK1 (JNK1)
NKP-1339 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for NKP-1339. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NKP-1339 through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [369]
COR-D [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for COR-D. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of COR-D through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [370]
2-(2-(butylamino)pyrimidin-4-ylamino)benzoic acid [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for 2-(2-(butylamino)pyrimidin-4-ylamino)benzoic acid. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 2-(2-(butylamino)pyrimidin-4-ylamino)benzoic acid through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [371]
2-(2-(pentyloxy)pyrimidin-4-ylamino)benzoic acid [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for 2-(2-(pentyloxy)pyrimidin-4-ylamino)benzoic acid. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 2-(2-(pentyloxy)pyrimidin-4-ylamino)benzoic acid through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [371]
2-(2-(phenylamino)pyrimidin-4-ylamino)benzamide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for 2-(2-(phenylamino)pyrimidin-4-ylamino)benzamide. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 2-(2-(phenylamino)pyrimidin-4-ylamino)benzamide through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [323]
2-(2-butoxypyrimidin-4-ylamino)benzoic acid [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for 2-(2-butoxypyrimidin-4-ylamino)benzoic acid. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 2-(2-butoxypyrimidin-4-ylamino)benzoic acid through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [371]
2-(2-phenoxypyrimidin-4-ylamino)benzoic acid [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for 2-(2-phenoxypyrimidin-4-ylamino)benzoic acid. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 2-(2-phenoxypyrimidin-4-ylamino)benzoic acid through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [371]
2-(2-propoxypyrimidin-4-ylamino)benzoic acid [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for 2-(2-propoxypyrimidin-4-ylamino)benzoic acid. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 2-(2-propoxypyrimidin-4-ylamino)benzoic acid through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [371]
2-(2-sec-butoxypyrimidin-4-ylamino)benzoic acid [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for 2-(2-sec-butoxypyrimidin-4-ylamino)benzoic acid. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 2-(2-sec-butoxypyrimidin-4-ylamino)benzoic acid through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [371]
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 Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for 4,5,6,7-tetrabromo-1H-benzo[d][1,2,3]triazole. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of 4,5,6,7-tetrabromo-1H-benzo[d][1,2,3]triazole through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [372]
Aminopyridine deriv. 2 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for Aminopyridine deriv. 2. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Aminopyridine deriv. 2 through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [373]
AS-601245 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for AS-601245. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AS-601245 through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [371]
Bisindolylmaleimide-I [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for Bisindolylmaleimide-I. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Bisindolylmaleimide-I through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [50], [92]
CI-1040 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for CI-1040. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of CI-1040 through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [370]
JNK-IN-8 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for JNK-IN-8. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of JNK-IN-8 through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [230]
KN-62 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for KN-62. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of KN-62 through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [327]
KT-5720 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for KT-5720. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of KT-5720 through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [374]
N-(4-amino-5-cyano-6-ethoxypyridin-2-yl)acetamide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for N-(4-amino-5-cyano-6-ethoxypyridin-2-yl)acetamide. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of N-(4-amino-5-cyano-6-ethoxypyridin-2-yl)acetamide through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [375]
N-(4-amino-5-cyano-6-phenylpyridin-2-yl)acetamide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for N-(4-amino-5-cyano-6-phenylpyridin-2-yl)acetamide. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of N-(4-amino-5-cyano-6-phenylpyridin-2-yl)acetamide through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [375]
N-(4-amino-6-butoxy-5-cyanopyridin-2-yl)acetamide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for N-(4-amino-6-butoxy-5-cyanopyridin-2-yl)acetamide. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of N-(4-amino-6-butoxy-5-cyanopyridin-2-yl)acetamide through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [323]
N-(6-ethoxypyridin-2-yl)acetamide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for N-(6-ethoxypyridin-2-yl)acetamide. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of N-(6-ethoxypyridin-2-yl)acetamide through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [375]
NM-PP1 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for NM-PP1. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of NM-PP1 through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [323]
Phylomers [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for Phylomers. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Phylomers through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [375]
RO-316233 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for RO-316233. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of RO-316233 through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [323]
Ro31-8220 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for Ro31-8220. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Ro31-8220 through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [50], [92]
STAUROSPORINONE [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase JNK1 (JNK1) is a therapeutic target for STAUROSPORINONE. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of STAUROSPORINONE through regulating the expression of Stress-activated protein kinase JNK1 (JNK1). [92], [323]
TGF-beta receptor type II (TGFBR2)
TGF-BR2 mab [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary TGF-beta receptor type II (TGFBR2) is a therapeutic target for TGF-BR2 mab. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of TGF-BR2 mab through regulating the expression of TGF-beta receptor type II (TGFBR2). [275], [376]
LY2109761 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary TGF-beta receptor type II (TGFBR2) is a therapeutic target for LY2109761. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of LY2109761 through regulating the expression of TGF-beta receptor type II (TGFBR2). [275], [377]
Transferrin receptor protein 1 (TFRC)
ABBV-CX-2029 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Transferrin receptor protein 1 (TFRC) is a therapeutic target for ABBV-CX-2029. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ABBV-CX-2029 through regulating the expression of Transferrin receptor protein 1 (TFRC). [378], [379]
Tyrosine-protein kinase UFO (AXL)
Gilteritinib [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Tyrosine-protein kinase UFO (AXL) is a therapeutic target for Gilteritinib. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Gilteritinib through regulating the expression of Tyrosine-protein kinase UFO (AXL). [380], [381]
Bemcentinib [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tyrosine-protein kinase UFO (AXL) is a therapeutic target for Bemcentinib. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Bemcentinib through regulating the expression of Tyrosine-protein kinase UFO (AXL). [380], [382]
BGB-324 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tyrosine-protein kinase UFO (AXL) is a therapeutic target for BGB-324. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BGB-324 through regulating the expression of Tyrosine-protein kinase UFO (AXL). [380], [383]
BI-505 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tyrosine-protein kinase UFO (AXL) is a therapeutic target for BI-505. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BI-505 through regulating the expression of Tyrosine-protein kinase UFO (AXL). [15], [380]
Enapotamab vedotin [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tyrosine-protein kinase UFO (AXL) is a therapeutic target for Enapotamab vedotin. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Enapotamab vedotin through regulating the expression of Tyrosine-protein kinase UFO (AXL). [380], [384]
MGCD265 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tyrosine-protein kinase UFO (AXL) is a therapeutic target for MGCD265. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of MGCD265 through regulating the expression of Tyrosine-protein kinase UFO (AXL). [145], [380]
ONO-7475 [Phase 1/2]
In total 2 mechanisms lead to this potential drug response
Response Summary Tyrosine-protein kinase UFO (AXL) is a therapeutic target for ONO-7475. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ONO-7475 through regulating the expression of Tyrosine-protein kinase UFO (AXL). [380], [385]
Tyrosine-protein kinase UFO (AXL) is a therapeutic target for ONO-7475. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of ONO-7475 through regulating the expression of Tyrosine-protein kinase UFO (AXL). [15], [380]
TP-0903 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tyrosine-protein kinase UFO (AXL) is a therapeutic target for TP-0903. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of TP-0903 through regulating the expression of Tyrosine-protein kinase UFO (AXL). [380], [386]
AVB-S6-500 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Tyrosine-protein kinase UFO (AXL) is a therapeutic target for AVB-S6-500. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of AVB-S6-500 through regulating the expression of Tyrosine-protein kinase UFO (AXL). [380], [387]
BPI-9016 M [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Tyrosine-protein kinase UFO (AXL) is a therapeutic target for BPI-9016 M. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of BPI-9016 M through regulating the expression of Tyrosine-protein kinase UFO (AXL). [15], [380]
DS-1205 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Tyrosine-protein kinase UFO (AXL) is a therapeutic target for DS-1205. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of DS-1205 through regulating the expression of Tyrosine-protein kinase UFO (AXL). [15], [380]
INCB81776 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Tyrosine-protein kinase UFO (AXL) is a therapeutic target for INCB81776. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of INCB81776 through regulating the expression of Tyrosine-protein kinase UFO (AXL). [380], [388]
PF-07265807 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Tyrosine-protein kinase UFO (AXL) is a therapeutic target for PF-07265807. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of PF-07265807 through regulating the expression of Tyrosine-protein kinase UFO (AXL). [380], [389]
RXDX-106 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Tyrosine-protein kinase UFO (AXL) is a therapeutic target for RXDX-106. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of RXDX-106 through regulating the expression of Tyrosine-protein kinase UFO (AXL). [380], [390]
Cu-anti-hAXL [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Tyrosine-protein kinase UFO (AXL) is a therapeutic target for Cu-anti-hAXL. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of Cu-anti-hAXL through regulating the expression of Tyrosine-protein kinase UFO (AXL). [15], [380]
DP-3975 [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Tyrosine-protein kinase UFO (AXL) is a therapeutic target for DP-3975. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of DP-3975 through regulating the expression of Tyrosine-protein kinase UFO (AXL). [380], [391]
GL21.T [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Tyrosine-protein kinase UFO (AXL) is a therapeutic target for GL21.T. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of GL21.T through regulating the expression of Tyrosine-protein kinase UFO (AXL). [380], [391]
YW327.6S2 [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Tyrosine-protein kinase UFO (AXL) is a therapeutic target for YW327.6S2. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of YW327.6S2 through regulating the expression of Tyrosine-protein kinase UFO (AXL). [380], [392]
LDC1267 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Tyrosine-protein kinase UFO (AXL) is a therapeutic target for LDC1267. The RNA demethylase ALKBH5 (ALKBH5) has potential in affecting the response of LDC1267 through regulating the expression of Tyrosine-protein kinase UFO (AXL). [380], [391]
References
Ref 1 ALKBH5 inhibited autophagy of epithelial ovarian cancer through miR-7 and BCL-2. J Exp Clin Cancer Res. 2019 Apr 15;38(1):163. doi: 10.1186/s13046-019-1159-2.
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 ALKBH5 promotes the proliferation of renal cell carcinoma by regulating AURKB expression in an m(6)A-dependent manner. Ann Transl Med. 2020 May;8(10):646. doi: 10.21037/atm-20-3079.
Ref 31 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 32 A phase I trial of AT9283 (a selective inhibitor of aurora kinases) in children and adolescents with solid tumors: a Cancer Research UK study. Clin Cancer Res. 2015 Jan 15;21(2):267-73. doi: 10.1158/1078-0432.CCR-14-1592. Epub 2014 Nov 4.
Ref 33 A phase I dose escalation study with anti-CD44v6 bivatuzumab mertansine in patients with incurable squamous cell carcinoma of the head and neck or esophagus. Clin Cancer Res. 2006 Oct 15;12(20 Pt 1):6064-72. doi: 10.1158/1078-0432.CCR-06-0910.
Ref 34 Preclinical characterization of ABT-348, a kinase inhibitor targeting the aurora, vascular endothelial growth factor receptor/platelet-derived growth factor receptor, and Src kinase families. J Pharmacol Exp Ther. 2012 Dec;343(3):617-27. doi: 10.1124/jpet.112.197087. Epub 2012 Aug 30.
Ref 35 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: 1936).
Ref 36 Clinical pipeline report, company report or official report of Cyclacel.
Ref 37 A phase 1 dose escalation study of BI 831266, an inhibitor of Aurora kinase B, in patients with advanced solid tumors. Invest New Drugs. 2015 Apr;33(2):409-22. doi: 10.1007/s10637-014-0201-7. Epub 2014 Dec 23.
Ref 38 doi: 10.1158/1535-7163.TARG-13-B281
Ref 39 Discovery of GSK1070916, a potent and selective inhibitor of Aurora B/C kinase. J Med Chem. 2010 May 27;53(10):3973-4001. doi: 10.1021/jm901870q.
Ref 40 Preclinical evaluation of AMG 900, a novel potent and highly selective pan-aurora kinase inhibitor with activity in taxane-resistant tumor cell lines. Cancer Res. 2010 Dec 1;70(23):9846-54. doi: 10.1158/0008-5472.CAN-10-3001. Epub 2010 Oct 8.
Ref 41 Phase I study of barasertib (AZD1152), a selective inhibitor of Aurora B kinase, in patients with advanced solid tumors. Invest New Drugs. 2013 Apr;31(2):370-80. doi: 10.1007/s10637-012-9825-7. Epub 2012 Jun 2.
Ref 42 Cell cycle kinases as therapeutic targets for cancer. Nat Rev Drug Discov. 2009 Jul;8(7):547-66. doi: 10.1038/nrd2907.
Ref 43 Clinical pipeline report, company report or official report of Takeda (2009).
Ref 44 Aurora kinase inhibitors: progress towards the clinic. Invest New Drugs. 2012 Dec;30(6):2411-32. doi: 10.1007/s10637-012-9798-6. Epub 2012 Feb 18.
Ref 45 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 46 Preclinical characterization of Aurora kinase inhibitor R763/AS703569 identified through an image-based phenotypic screen. J Cancer Res Clin Oncol. 2010 Jan;136(1):99-113. doi: 10.1007/s00432-009-0641-1.
Ref 47 Potent and selective Aurora inhibitors identified by the expansion of a novel scaffold for protein kinase inhibition. J Med Chem. 2005 Apr 21;48(8):3080-4. doi: 10.1021/jm049076m.
Ref 48 An integrated computational approach to the phenomenon of potent and selective inhibition of aurora kinases B and C by a series of 7-substituted indirubins. J Med Chem. 2007 Aug 23;50(17):4027-37. doi: 10.1021/jm070077z. Epub 2007 Aug 1.
Ref 49 Discovery of novel and potent thiazoloquinazolines as selective Aurora A and B kinase inhibitors. J Med Chem. 2006 Feb 9;49(3):955-70. doi: 10.1021/jm050786h.
Ref 50 The selectivity of protein kinase inhibitors: a further update. Biochem J. 2007 Dec 15;408(3):297-315. doi: 10.1042/BJ20070797.
Ref 51 US patent application no. 7,375,212, Modulation of Aurora B expression.
Ref 52 Discovery of orally bioavailable imidazo[1,2-a]pyrazine-based Aurora kinase inhibitors. Bioorg Med Chem Lett. 2010 Nov 15;20(22):6739-43. doi: 10.1016/j.bmcl.2010.08.140. Epub 2010 Sep 18.
Ref 53 Discovery of a new series of Aurora inhibitors through truncation of GSK1070916. Bioorg Med Chem Lett. 2010 Apr 15;20(8):2552-5. doi: 10.1016/j.bmcl.2010.02.091. Epub 2010 Mar 1.
Ref 54 SNS-314, a pan-Aurora kinase inhibitor, shows potent anti-tumor activity and dosing flexibility in vivo. Cancer Chemother Pharmacol. 2010 Mar;65(4):707-17. doi: 10.1007/s00280-009-1076-8. Epub 2009 Aug 1.
Ref 55 Ethionine-mediated reduction of S-adenosylmethionine is responsible for the neural tube defects in the developing mouse embryo-mediated m6A modification and is involved in neural tube defects via modulating Wnt/Beta-catenin signaling pathway. Epigenetics Chromatin. 2021 Dec 4;14(1):52. doi: 10.1186/s13072-021-00426-3.
Ref 56 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 57 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 58 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
Ref 59 BMP2 Modified by the m(6)A Demethylation Enzyme ALKBH5 in the Ossification of the Ligamentum Flavum Through the AKT Signaling Pathway. Calcif Tissue Int. 2020 May;106(5):486-493. doi: 10.1007/s00223-019-00654-6. Epub 2020 Jan 2.
Ref 60 Synthesis and structure-activity relationship studies of N-benzyl-2-phenylpyrimidin-4-amine derivatives as potent USP1/UAF1 deubiquitinase inhibitors with anticancer activity against nonsmall cell lung cancer. J Med Chem. 2014 Oct 9;57(19):8099-110. doi: 10.1021/jm5010495. Epub 2014 Sep 17.
Ref 61 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 62 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 63 RNA Demethylase ALKBH5 Prevents Lung Cancer Progression by Regulating EMT and Stemness via Regulating p53. Front Oncol. 2022 Apr 22;12:858694. doi: 10.3389/fonc.2022.858694. eCollection 2022.
Ref 64 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 65 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 66 A review of contusugene ladenovec (Advexin) p53 therapy. Curr Opin Mol Ther. 2009 Feb;11(1):54-61.
Ref 67 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 68 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 69 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 70 The Protein Data Bank. Nucleic Acids Res. 2000 Jan 1;28(1):235-42. doi: 10.1093/nar/28.1.235.
Ref 71 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 72 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 73 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 74 WO patent application no. 2013,1850,32, Nanotherapeutics for drug targeting.
Ref 75 National Cancer Institute Drug Dictionary (drug id 761551).
Ref 76 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 77 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 78 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 79 2011 Pipeline of Quark Pharm.
Ref 80 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 81 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 82 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 83 Regulation of host gene expression by HIV-1 TAR microRNAs. Retrovirology. 2013; 10: 86.
Ref 84 Prevent Oral Cancer With Mouthwash. Introgen Therapeutics.
Ref 85 ALKBH5-mediated m6A-demethylation of USP1 regulated T-cell acute lymphoblastic leukemia cell glucocorticoid resistance by Aurora B. Mol Carcinog. 2021 Sep;60(9):644-657. doi: 10.1002/mc.23330. Epub 2021 Jun 25.
Ref 86 Chemogenomic identification of Ref-1/AP-1 as a therapeutic target for asthma. Proc Natl Acad Sci U S A. 2003 Feb 4;100(3):1169-73. doi: 10.1073/pnas.0437889100. Epub 2003 Jan 24.
Ref 87 m6A hypomethylation of DNMT3B regulated by ALKBH5 promotes intervertebral disc degeneration via E4F1 deficiency. Clin Transl Med. 2022 Mar;12(3):e765. doi: 10.1002/ctm2.765.
Ref 88 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 89 Novel and selective DNA methyltransferase inhibitors: Docking-based virtual screening and experimental evaluation. Bioorg Med Chem. 2010 Jan 15;18(2):822-9. doi: 10.1016/j.bmc.2009.11.050. Epub 2009 Nov 27.
Ref 90 SAR around (l)-S-adenosyl-l-homocysteine, an inhibitor of human DNA methyltransferase (DNMT) enzymes. Bioorg Med Chem Lett. 2009 May 15;19(10):2747-51. doi: 10.1016/j.bmcl.2009.03.113. Epub 2009 Mar 28.
Ref 91 Constrained (l-)-S-adenosyl-l-homocysteine (SAH) analogues as DNA methyltransferase inhibitors. Bioorg Med Chem Lett. 2009 May 15;19(10):2742-6.
Ref 92 Post-translational modification of RNA m6A demethylase ALKBH5 regulates ROS-induced DNA damage response. Nucleic Acids Res. 2021 Jun 4;49(10):5779-5797. doi: 10.1093/nar/gkab415.
Ref 93 National Cancer Institute Drug Dictionary (drug name SEphB4-HSA).
Ref 94 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 95 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 96 Clinical pipeline report, company report or official report of GlaxoSmithKline (2009).
Ref 97 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 98 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 99 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 100 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 101 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 102 Emerging drugs for diabetic foot ulcers. Expert Opin Emerg Drugs. 2006 Nov;11(4):709-24. doi: 10.1517/14728214.11.4.709.
Ref 103 Boehringer Ingelheim. Product Development Pipeline. June 2 2009.
Ref 104 Nasopharyngeal carcinoma: Current treatment options and future directions. J Nasopharyng Carcinoma, 2014, 1(16): e16.
Ref 105 Quantitative prediction of fold resistance for inhibitors of EGFR. Biochemistry. 2009 Sep 8;48(35):8435-48. doi: 10.1021/bi900729a.
Ref 106 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 107 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 108 Clinical pipeline report, company report or official report of Ionis Pharmaceuticals.
Ref 109 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 110 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 111 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 112 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 113 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 114 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 115 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 116 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 117 Marine-Sourced Anti-Cancer and Cancer Pain Control Agents in Clinical and Late Preclinical Development. Mar Drugs. 2014 January; 12(1): 255-278.
Ref 118 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 119 Clinical pipeline report, company report or official report of EpimAb Biotherapeutics.
Ref 120 ClinicalTrials.gov (NCT03152435) EGFR CART Cells for Patients With Metastatic Colorectal Cancer
Ref 121 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 122 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
Ref 123 Clinical pipeline report, company report or official report of Zentalis Pharmaceuticals.
Ref 124 ClinicalTrials.gov (NCT01869166) Treatment of Chemotherapy Refractory EGFR(Epidermal Growth Factor Receptor) Positive Advanced Solid Tumors (CART-EGFR)
Ref 125 BiPar Sciences Co-founder Reunites Management Team At TriAct Therapeutics to Advance Clinical Stage Cancer Programs. TriAct Therapeutics. Sept. 10, 2009.
Ref 126 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 127 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 128 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 129 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 130 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 131 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 132 Clinical pipeline report, company report or official report of Black Diamond Therapeutics.
Ref 133 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 134 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 135 Clinical pipeline report, company report or official report of Affimed Therapeutics.
Ref 136 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 137 ClinicalTrials.gov (NCT03638167) EGFR806-specific CAR T Cell Locoregional Immunotherapy for EGFR-positive Recurrent or Refractory Pediatric CNS Tumors
Ref 138 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 139 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 140 World Antibody-Drug Conjugate Summit, October 15-16, 2013, San Francisco, CA. MAbs. 2014 January 1; 6(1): 18-29.
Ref 141 Company report (Biooncology)
Ref 142 Clinical pipeline report, company report or official report of SystImmune.
Ref 143 Bispecific antibodies rise again. Nat Rev Drug Discov. 2014 Nov;13(11):799-801. doi: 10.1038/nrd4478.
Ref 144 Clinical pipeline report, company report or official report of Merus.
Ref 145 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
Ref 146 ClinicalTrials.gov (NCT02331693) CAR T Cells in Treating Patients With Malignant Gliomas Overexpressing EGFR
Ref 147 National Cancer Institute Drug Dictionary (drug id 596693).
Ref 148 Clinical pipeline report, company report or official report of Shionogi (2011).
Ref 149 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 150 Antitumor Effects of EGFR Antisense Guanidine-Based Peptide Nucleic Acids in Cancer Models. ACS Chem Biol. 2013 February 15; 8(2): 345-352.
Ref 151 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 152 Clinical pipeline report, company report or official report of Bristol-Myers Squibb.
Ref 153 Protein-tyrosine kinase inhibition: mechanism-based discovery of antitumor agents. J Nat Prod. 1992 Nov;55(11):1529-60. doi: 10.1021/np50089a001.
Ref 154 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 155 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 156 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 157 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 158 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 159 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 160 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 161 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 162 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 163 Novel antiproliferative agents derived from lavendustin A. J Med Chem. 1994 Nov 25;37(24):4079-84. doi: 10.1021/jm00050a005.
Ref 164 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 165 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 166 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 167 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 168 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 169 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 170 Selected novel anticancer treatments targeting cell signaling proteins. Oncologist. 2001;6(6):517-37. doi: 10.1634/theoncologist.6-6-517.
Ref 171 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 172 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 173 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 174 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 175 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 176 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 177 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 178 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 179 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 180 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 181 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 182 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 183 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 184 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 185 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 186 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 187 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 188 Effects of hEGF (MG111) on gastric mucosal potential difference in rats. Scand J Gastroenterol Suppl. 1989;162:198-201. doi: 10.3109/00365528909091160.
Ref 189 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 190 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 191 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 192 WO patent application no. 2009,0582,67, Benzomorpholine derivatives and methods of use.
Ref 193 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 194 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 195 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 196 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 197 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 198 ALKBH5 promotes lung fibroblast activation and silica-induced pulmonary fibrosis through miR-320a-3p and FOXM1. Cell Mol Biol Lett. 2022 Mar 12;27(1):26. doi: 10.1186/s11658-022-00329-5.
Ref 199 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: 1443).
Ref 200 N(6)-Methylation of Adenosine of FZD10 mRNA Contributes to PARP Inhibitor Resistance. Cancer Res. 2019 Jun 1;79(11):2812-2820. doi: 10.1158/0008-5472.CAN-18-3592. Epub 2019 Apr 9.
Ref 201 ALKBH5-Modified HMGB1-STING Activation Contributes to Radiation Induced Liver Disease via Innate Immune Response. Int J Radiat Oncol Biol Phys. 2021 Oct 1;111(2):491-501. doi: 10.1016/j.ijrobp.2021.05.115. Epub 2021 May 24.
Ref 202 Avontec Announces Results of a Multiple Dose Clinical Phase I Study with Its Drug Candidate AVT-02 UE Ointment After Topical Treatment in Male Healthy Volunteers. Avontec. 2008.
Ref 203 Hypoxia induces an endometrial cancer stem-like cell phenotype via HIF-dependent demethylation of SOX2 mRNA. Oncogenesis. 2020 Sep 11;9(9):81. doi: 10.1038/s41389-020-00265-z.
Ref 204 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 205 A RNA antagonist of hypoxia-inducible factor-1alpha, EZN-2968, inhibits tumor cell growth. Mol Cancer Ther. 2008 Nov;7(11):3598-608. doi: 10.1158/1535-7163.MCT-08-0510. Epub 2008 Oct 30.
Ref 206 CRLX101, an investigational camptothecin-containing nanoparticle-drug conjugate, targets cancer stem cells and impedes resistance to antiangiogenic therapy in mouse models of breast cancer. Breast Cancer Res Treat. 2015 Apr;150(3):559-67. doi: 10.1007/s10549-015-3349-8. Epub 2015 Apr 2.
Ref 207 The biology and chemistry of hyperlipidemia. Bioorg Med Chem. 2007 Jul 15;15(14):4674-99. doi: 10.1016/j.bmc.2007.04.031. Epub 2007 Apr 25.
Ref 208 Pilot trial of EZN-2968, an antisense oligonucleotide inhibitor of hypoxia-inducible factor-1 alpha (HIF-1Alpha), in patients with refractory solid tumors. Cancer Chemother Pharmacol. 2014 Feb;73(2):343-8. doi: 10.1007/s00280-013-2362-z. Epub 2013 Nov 30.
Ref 209 2-methoxyestradiol inhibits hypoxia-inducible factor 1alpha, tumor growth, and angiogenesis and augments paclitaxel efficacy in head and neck squamous cell carcinoma. Clin Cancer Res. 2004 Dec 15;10(24):8665-73. doi: 10.1158/1078-0432.CCR-04-1393.
Ref 210 ENMD-1198, a new analogue of 2-methoxyestradiol, displays both antiangiogenic and vascular-disrupting properties. Mol Cancer Ther. 2010 May;9(5):1408-18. doi: 10.1158/1535-7163.MCT-09-0894. Epub 2010 May 4.
Ref 211 US patent application no. 7,217,572, Modulation of HIF1.alpha. and HIF2.alpha. expression.
Ref 212 Synthesis of (aryloxyacetylamino)-isonicotinic/nicotinic acid analogues as potent hypoxia-inducible factor (HIF)-1alpha inhibitors. Bioorg Med Chem Lett. 2007 Nov 15;17(22):6305-10. doi: 10.1016/j.bmcl.2007.09.005. Epub 2007 Sep 7.
Ref 213 ALKBH5 regulates IGF1R expression to promote the Proliferation and Tumorigenicity of Endometrial Cancer. J Cancer. 2020 Jul 25;11(19):5612-5622. doi: 10.7150/jca.46097. eCollection 2020.
Ref 214 2005 approvals: Safety first. Nature Reviews Drug Discovery 5, 92-93 (February 2006).
Ref 215 IGF-1R, IGF-1 and IGF-2 expression as potential prognostic and predictive markers in colorectal-cancer. Virchows Arch. 2003 Aug;443(2):139-45. doi: 10.1007/s00428-003-0856-5. Epub 2003 Jul 5.
Ref 216 Imidazo[2,1-b]thiazoles: multitargeted inhibitors of both the insulin-like growth factor receptor and members of the epidermal growth factor family... Bioorg Med Chem Lett. 2010 Apr 15;20(8):2452-5.
Ref 217 MM-141, an IGF-IR- and ErbB3-directed bispecific antibody, overcomes network adaptations that limit activity of IGF-IR inhibitors. Mol Cancer Ther. 2014 Feb;13(2):410-25. doi: 10.1158/1535-7163.MCT-13-0255. Epub 2013 Nov 26.
Ref 218 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
Ref 219 Clinical Phase I study with an Insulin-like Growth Factor-1 receptor inhibitor: experiences in patients with squamous non-small cell lung carcinoma. Acta Oncol. 2011 Apr;50(3):441-7. doi: 10.3109/0284186X.2010.499370. Epub 2010 Aug 11.
Ref 220 Doxorubicin plus the IGF-1R antibody cixutumumab in soft tissue sarcoma: a phase I study using the TITE-CRM model. Ann Oncol. 2015 Jul;26(7):1459-64. doi: 10.1093/annonc/mdv171. Epub 2015 Apr 9.
Ref 221 Mecasermin rinfabate: insulin-like growth factor-I/insulin-like growth factor binding protein-3, mecaserimin rinfibate, rhIGF-I/rhIGFBP-3. Drugs R D. 2005;6(2):120-7. doi: 10.2165/00126839-200506020-00008.
Ref 222 A phase 1, open-label, dose-escalation study of BIIB022 (anti-IGF-1R monoclonal antibody) in subjects with relapsed or refractory solid tumors. Invest New Drugs. 2014 Jun;32(3):518-25. doi: 10.1007/s10637-014-0064-y. Epub 2014 Jan 24.
Ref 223 A primary adrenal steroid, 11beta-hydroxyandrostenedione, has an osteotropic effect and little androgenic activity. J Steroid Biochem Mol Biol. 2000 Nov 15;74(4):203-11. doi: 10.1016/s0960-0760(00)00124-2.
Ref 224 Clinical pipeline report, company report or official report of Amgen (2009).
Ref 225 Clinical pipeline report, company report or official report of Fusion Pharmaceuticals.
Ref 226 The cyclolignan picropodophyllin attenuates intimal hyperplasia after rat carotid balloon injury by blocking insulin-like growth factor-1 receptor signaling. J Vasc Surg. 2007 Jul;46(1):108-15. doi: 10.1016/j.jvs.2007.02.066.
Ref 227 ATP non-competitive IGF-1 receptor kinase inhibitors as lead anti-neoplastic and anti-papilloma agents. Eur J Pharmacol. 2007 May 7;562(1-2):1-11. doi: 10.1016/j.ejphar.2007.01.052. Epub 2007 Feb 3.
Ref 228 Discovery and evaluation of 4-(2-(4-chloro-1H-pyrazol-1-yl)ethylamino)-3-(6-(1-(3-fluoropropyl)piperidin-4-yl)-4-methyl-1H-benzo[d]imidazol-2-yl)pyridin-2(1H)-one (BMS-695735), an orally efficacious inhibitor of insulin-like growth factor-1 receptor kinase with broad spectrum in vivo antitumor activity. J Med Chem. 2008 Oct 9;51(19):5897-900. doi: 10.1021/jm800832q. Epub 2008 Sep 3.
Ref 229 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: 1801).
Ref 230 How many drug targets are there Nat Rev Drug Discov. 2006 Dec;5(12):993-6.
Ref 231 Clinical pipeline report, company report or official report of Antisense Therapeutics.
Ref 232 Specific inhibition of insulin-like growth factor-1 and insulin receptor tyrosine kinase activity and biological function by tyrphostins. Endocrinology. 1997 Apr;138(4):1427-33. doi: 10.1210/endo.138.4.5092.
Ref 233 Comprehensive analysis of kinase inhibitor selectivity. Nat Biotechnol. 2011 Oct 30;29(11):1046-51. doi: 10.1038/nbt.1990.
Ref 234 SAR of PXR transactivation in benzimidazole-based IGF-1R kinase inhibitors. Bioorg Med Chem Lett. 2010 Mar 1;20(5):1744-8. doi: 10.1016/j.bmcl.2010.01.087. Epub 2010 Jan 21.
Ref 235 Optimization of a series of 4,6-bis-anilino-1H-pyrrolo[2,3-d]pyrimidine inhibitors of IGF-1R: elimination of an acid-mediated decomposition pathway. Bioorg Med Chem Lett. 2009 Jan 15;19(2):373-7. doi: 10.1016/j.bmcl.2008.11.065. Epub 2008 Nov 24.
Ref 236 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800031207)
Ref 237 Insulin-like growth factor-1 receptor inhibition induces a resistance mechanism via the epidermal growth factor receptor/HER3/AKT signaling pathway: rational basis for cotargeting insulin-like growth factor-1 receptor and epidermal growth factor receptor in hepatocellular carcinoma. Clin Cancer Res. 2009 Sep 1;15(17):5445-56. doi: 10.1158/1078-0432.CCR-08-2980. Epub 2009 Aug 25.
Ref 238 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 239 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 240 2014 FDA drug approvals. Nat Rev Drug Discov. 2015 Feb;14(2):77-81. doi: 10.1038/nrd4545.
Ref 241 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services.
Ref 242 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 243 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 244 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 245 PEGylated interferon beta-1a in the treatment of multiple sclerosis - an update. Biologics. 2013; 7: 131-138.
Ref 246 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 247 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
Ref 248 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 249 ALKBH5-HOXA10 loop-mediated JAK2 m6A demethylation and cisplatin resistance in epithelial ovarian cancer. J Exp Clin Cancer Res. 2021 Sep 8;40(1):284. doi: 10.1186/s13046-021-02088-1.
Ref 250 Inhibitors of JAK-family kinases: an update on the patent literature 2013-2015, part 1. Expert Opin Ther Pat. 2017 Feb;27(2):127-143. doi: 10.1080/13543776.2017.1252753. Epub 2016 Nov 7.
Ref 251 2011 FDA drug approvals. Nat Rev Drug Discov. 2012 Feb 1;11(2):91-4. doi: 10.1038/nrd3657.
Ref 252 Selective JAK inhibitors in development for rheumatoid arthritis. Expert Opin Investig Drugs. 2014 Aug;23(8):1067-77. doi: 10.1517/13543784.2014.918604. Epub 2014 May 12.
Ref 253 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2019
Ref 254 National Cancer Institute Drug Dictionary (drug id 609888).
Ref 255 Genetic determinants of response and survival in momelotinib-treated patients with myelofibrosis. Leukemia. 2015 Mar;29(3):741-4. doi: 10.1038/leu.2014.306. Epub 2014 Nov 11.
Ref 256 Emerging drugs for the therapy of primary and post essential thrombocythemia, post polycythemia vera myelofibrosis. Expert Opin Emerg Drugs. 2009 Sep;14(3):471-9. doi: 10.1517/14728210903066809.
Ref 257 Clinical pipeline report, company report or official report of Concert Pharmaceuticals.
Ref 258 Discovery and characterization of LY2784544, a small-molecule tyrosine kinase inhibitor of JAK2V617F. Blood Cancer J. 2013 Apr 12;3(4):e109. doi: 10.1038/bcj.2013.6.
Ref 259 The JAK2 inhibitor AZD1480 potently blocks Stat3 signaling and oncogenesis in solid tumors. Cancer Cell. 2009 Dec 8;16(6):487-97. doi: 10.1016/j.ccr.2009.10.015.
Ref 260 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: 2048).
Ref 261 Characterization of BMS-911543, a functionally selective small-molecule inhibitor of JAK2. Leukemia. 2012 Feb;26(2):280-8. doi: 10.1038/leu.2011.292. Epub 2011 Oct 21.
Ref 262 Company report (Portola Pharmaceuticals)
Ref 263 Effect of NS-018, a selective JAK2V617F inhibitor, in a murine model of myelofibrosis. Blood Cancer J. 2014 Jan 10;4(1):e174. doi: 10.1038/bcj.2013.73.
Ref 264 Comparison of mutated ABL1 and JAK2 as oncogenes and drug targets in myeloproliferative disorders. Leukemia. 2008 Jul;22(7):1320-34. doi: 10.1038/leu.2008.133. Epub 2008 Jun 5.
Ref 265 Jak2 tyrosine kinase mediates oxidative stress-induced apoptosis in vascular smooth muscle cells. J Biol Chem. 2004 Aug 13;279(33):34547-52. doi: 10.1074/jbc.M405045200. Epub 2004 May 24.
Ref 266 Janus kinase 2 inhibitors. Synthesis and characterization of a novel polycyclic azaindole. J Med Chem. 2009 Dec 24;52(24):7938-41. doi: 10.1021/jm901383u.
Ref 267 In silico identification and biochemical evaluation of novel inhibitors of NRH:quinone oxidoreductase 2 (NQO2). Bioorg Med Chem Lett. 2010 Dec 15;20(24):7331-6.
Ref 268 Effects of the JAK2 inhibitor, AZ960, on Pim/BAD/BCL-xL survival signaling in the human JAK2 V617F cell line SET-2. J Biol Chem. 2008 Nov 21;283(47):32334-43. doi: 10.1074/jbc.M803813200. Epub 2008 Sep 4.
Ref 269 The use of anti-inflammatory drugs in the treatment of people with severe coronavirus disease 2019 (COVID-19): The Perspectives of clinical immunologists from China. Clin Immunol. 2020 May;214:108393. doi: 10.1016/j.clim.2020.108393. Epub 2020 Mar 25.
Ref 270 Photochemical preparation of a pyridone containing tetracycle: a Jak protein kinase inhibitor. Bioorg Med Chem Lett. 2002 Apr 22;12(8):1219-23. doi: 10.1016/s0960-894x(02)00106-3.
Ref 271 Identification of 1,2,3,4,5,6-hexabromocyclohexane as a small molecule inhibitor of jak2 tyrosine kinase autophosphorylation [correction of autophophorylation]. J Med Chem. 2005 Apr 7;48(7):2526-33. doi: 10.1021/jm049470k.
Ref 272 A Non-ATP-Competitive Dual Inhibitor of JAK2 and BCR-ABL Kinases: Elucidation of a Novel Therapeutic Spectrum Based on Substrate Competitive Inhibition. Genes Cancer. 2010 Apr;1(4):331-45. doi: 10.1177/1947601910371337.
Ref 273 Discovery of 1-methyl-1H-imidazole derivatives as potent Jak2 inhibitors. J Med Chem. 2014 Jan 9;57(1):144-58. doi: 10.1021/jm401546n. Epub 2013 Dec 20.
Ref 274 Hypoxia-inducible factors regulate pluripotency factor expression by ZNF217- and ALKBH5-mediated modulation of RNA methylation in breast cancer cells. Oncotarget. 2016 Oct 4;7(40):64527-64542. doi: 10.18632/oncotarget.11743.
Ref 275 RNA demethylase ALKBH5 inhibits TGF-Beta-induced EMT by regulating TGF-Beta/SMAD signaling in non-small cell lung?cancer. FASEB J. 2022 May;36(5):e22283. doi: 10.1096/fj.202200005RR.
Ref 276 US patent application no. 6,277,636, Antisense inhibition of MADH6 expression.
Ref 277 Dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A) inhibitors: a survey of recent patent literature. Expert Opin Ther Pat. 2017 Nov;27(11):1183-1199. doi: 10.1080/13543776.2017.1360285. Epub 2017 Aug 2.
Ref 278 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: 2824).
Ref 279 Characterization of SIS3, a novel specific inhibitor of Smad3, and its effect on transforming growth factor-beta1-induced extracellular matrix expression. Mol Pharmacol. 2006 Feb;69(2):597-607. doi: 10.1124/mol.105.017483. Epub 2005 Nov 15.
Ref 280 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2019
Ref 281 Targeting the phosphoinositide 3-kinase pathway in cancer. Nat Rev Drug Discov. 2009 Aug;8(8):627-44. doi: 10.1038/nrd2926.
Ref 282 Company report (BioOncology)
Ref 283 Company report (Lilly)
Ref 284 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 285 National Cancer Institute Drug Dictionary (drug id 714372).
Ref 286 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 287 In vitro anticancer activity of PI3K alpha selective inhibitor BYL719 in head and neck cancer. Anticancer Res. 2015 Jan;35(1):175-82.
Ref 288 M(6)A Demethylase ALKBH5 Regulates PD-L1 Expression and Tumor Immunoenvironment in Intrahepatic Cholangiocarcinoma. Cancer Res. 2021 Sep 15;81(18):4778-4793. doi: 10.1158/0008-5472.CAN-21-0468. Epub 2021 Jul 23.
Ref 289 PD-1 as a potential target in cancer therapy. Cancer Med. 2013 October; 2(5): 662-673.
Ref 290 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2019
Ref 291 Development of Inhibitors of the Programmed Cell Death-1/Programmed Cell Death-Ligand 1 Signaling Pathway.J Med Chem. 2019 Feb 28;62(4):1715-1730.
Ref 292 Antibody-Dependent Cellular Cytotoxicity Activity of a Novel Anti-PD-L1 Antibody Avelumab (MSB0010718C) on Human Tumor Cells. Cancer Immunol Res. 2015 Oct;3(10):1148-1157. doi: 10.1158/2326-6066.CIR-15-0059. Epub 2015 May 26.
Ref 293 ClinicalTrials.gov (NCT03403777) Avelumab in Refractory Testicular Germ Cell Cancer.. U.S. National Institutes of Health.
Ref 294 A patent review on PD-1/PD-L1 antagonists: small molecules, peptides, and macrocycles (2015-2018). Expert Opin Ther Pat. 2018 Sep;28(9):665-678. doi: 10.1080/13543776.2018.1512706. Epub 2018 Sep 10.
Ref 295 Targeted immunotherapy for non-small cell lung cancer. World J Clin Oncol. 2014 May 10; 5(2): 39-47.
Ref 296 GEMSTONE-301: a phase III clinical trial of CS1001 as consolidation therapy in patients with locally advanced/unresectable (stage III) non-small cell lung cancer (NSCLC) who did not have disease progression after prior concurrent/sequential chemoradiotherapy. Transl Lung Cancer Res. 2020 Oct;9(5):2008-2015. doi: 10.21037/tlcr-20-608.
Ref 297 Clinical pipeline report, company report or official report of Gilead Sciences.
Ref 298 National Cancer Institute Drug Dictionary (drug id 740856).
Ref 299 National Cancer Institute Drug Dictionary (drug name INCB086550).
Ref 300 Clinical pipeline report, company report or official report of Numab Therapeutics.
Ref 301 Bintrafusp Alfa, a Bifunctional Fusion Protein Targeting TGF-Beta and PD-L1, in Second-Line Treatment of Patients With NSCLC: Results From an Expansion Cohort of a Phase 1 Trial. J Thorac Oncol. 2020 Jul;15(7):1210-1222. doi: 10.1016/j.jtho.2020.03.003. Epub 2020 Mar 13.
Ref 302 PD-1 blockade by CT-011, anti-PD-1 antibody, enhances ex vivo T-cell responses to autologous dendritic cell/myeloma fusion vaccine. J Immunother. 2011 Jun;34(5):409-18. doi: 10.1097/CJI.0b013e31821ca6ce.
Ref 303 Clinical pipeline report, company report or official report of Shattuck Labs.
Ref 304 ClinicalTrials.gov (NCT02937844) Pilot Study of Autologous Chimeric Switch Receptor Modified T Cells in Recurrent Glioblastoma Multiforme
Ref 305 Clinical pipeline report, company report or official report of Genmab.
Ref 306 CA-170 - A Potent Small-Molecule PD-L1 Inhibitor or Not?. Molecules. 2019 Aug 1;24(15):2804. doi: 10.3390/molecules24152804.
Ref 307 ClinicalTrials.gov (NCT04050709) QUILT 3.064: PD-L1 t-haNK In Subjects With Locally Advanced Or Metastatic Solid Cancers. U.S. National Institutes of Health.
Ref 308 Clinical pipeline report, company report or official report of Alpine Immune Sciences.
Ref 309 Clinical pipeline report, company report or official report of Inhibrx.
Ref 310 Clinical pipeline report, company report or official report of BeiGene.
Ref 311 Phase 1 Study of CK-301 (Cosibelimab) as a Single Agent in Subjects With Advanced Cancers
Ref 312 Clinical pipeline report, company report or official report of Innovent.
Ref 313 Safety and activity of anti-PD-L1 antibody in patients with advanced cancer. N Engl J Med. 2012 Jun 28;366(26):2455-65. doi: 10.1056/NEJMoa1200694. Epub 2012 Jun 2.
Ref 314 Clinical pipeline report, company report or official report of Kadmon.
Ref 315 Safety and Immunogenicity of LY3415244, a Bispecific Antibody Against TIM-3 and PD-L1, in Patients With Advanced Solid Tumors. Clin Cancer Res. 2021 May 15;27(10):2773-2781. doi: 10.1158/1078-0432.CCR-20-3716. Epub 2021 Jan 13.
Ref 316 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 317 ALKBH5-mediated m(6)A demethylation of KCNK15-AS1 inhibits pancreatic cancer progression via regulating KCNK15 and PTEN/AKT signaling. Cell Death Dis. 2021 Dec 1;12(12):1121. doi: 10.1038/s41419-021-04401-4.
Ref 318 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 319 CenterWatch. Drugs in Clinical Trials Database. CenterWatch. 2008.
Ref 320 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 321 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 322 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 323 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 324 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 325 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 326 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 327 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 328 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 329 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 330 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 331 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 332 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 333 ALKBH5 regulates STAT3 activity to affect the proliferation and tumorigenicity of osteosarcoma via an m6A-YTHDF2-dependent manner. EBioMedicine. 2022 Jun;80:104019. doi: 10.1016/j.ebiom.2022.104019. Epub 2022 Apr 28.
Ref 334 A STAT inhibitor patent review: progress since 2011.Expert Opin Ther Pat. 2015;25(12):1397-421.
Ref 335 [Effects of acitretin on the expression of signaling pathway-related genes in epidermal squamous-cell carcinoma cells]. Zhonghua Zhong Liu Za Zhi. 2006 Jan;28(1):21-4.
Ref 336 OPB-31121, a novel small molecular inhibitor, disrupts the JAK2/STAT3 pathway and exhibits an antitumor activity in gastric cancer cells. Cancer Lett. 2013 Jul 10;335(1):145-52. doi: 10.1016/j.canlet.2013.02.010. Epub 2013 Feb 10.
Ref 337 Clinical pipeline report, company report or official report of Purple Biotech.
Ref 338 US patent application no. 7,098,192, Antisense oligonucleotide modulation of STAT3 expression.
Ref 339 National Cancer Institute Drug Dictionary (drug id 617379).
Ref 340 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: 1768).
Ref 341 Napabucasin, a novel STAT3 inhibitor suppresses proliferation, invasion and stemness of glioblastoma cells. J Exp Clin Cancer Res. 2019 Jul 5;38(1):289. doi: 10.1186/s13046-019-1289-6.
Ref 342 Clinical pipeline report, company report or official report of Moleculin Biotech.
Ref 343 Phase I and biomarker study of OPB-51602, a novel signal transducer and activator of transcription (STAT) 3 inhibitor, in patients with refractory solid malignancies. Ann Oncol. 2015 May;26(5):998-1005. doi: 10.1093/annonc/mdv026. Epub 2015 Jan 21.
Ref 344 Phase I Dose-Finding Study of OPB-111077, a Novel STAT3 Inhibitor, in Patients with Advanced Hepatocellular Carcinoma. Cancer Res Treat. 2019 Apr;51(2):510-518. doi: 10.4143/crt.2018.226. Epub 2018 Jun 13.
Ref 345 Clinical pipeline report, company report or official report of Gastroenterology.
Ref 346 ALKBH5 Regulates SPHK1-Dependent Endothelial Cell Angiogenesis Following Ischemic Stress. Front Cardiovasc Med. 2022 Jan 20;8:817304. doi: 10.3389/fcvm.2021.817304. eCollection 2021.
Ref 347 Sphingosine kinase inhibitors: a review of patent literature (2006-2015). Expert Opin Ther Pat. 2016 Dec;26(12):1409-1416. doi: 10.1080/13543776.2016.1226282. Epub 2016 Aug 30.
Ref 348 Phosphorylation of the immunomodulatory drug FTY720 by sphingosine kinases. J Biol Chem. 2003 Nov 28;278(48):47408-15. doi: 10.1074/jbc.M307687200. Epub 2003 Sep 16.
Ref 349 Characterization of B-5354c, a new sphingosine kinase inhibitor, produced by a marine bacterium. J Antibiot (Tokyo). 2000 Aug;53(8):759-64. doi: 10.7164/antibiotics.53.759.
Ref 350 Modulation of cellular S1P levels with a novel, potent and specific inhibitor of sphingosine kinase-1. Biochem J. 2012 May 15;444(1):79-88. doi: 10.1042/BJ20111929.
Ref 351 A selective sphingosine kinase 1 inhibitor integrates multiple molecular therapeutic targets in human leukemia. Blood. 2008 Aug 15;112(4):1382-91. doi: 10.1182/blood-2008-02-138958. Epub 2008 May 29.
Ref 352 F-12509A, a new sphingosine kinase inhibitor, produced by a discomycete. J Antibiot (Tokyo). 2000 May;53(5):459-66. doi: 10.7164/antibiotics.53.459.
Ref 353 Sphingosine kinase 1 is a potential therapeutic target for nasopharyngeal carcinoma. Oncotarget. 2016 Dec 6;7(49):80586-80598. doi: 10.18632/oncotarget.13014.
Ref 354 ALKBH5 is a mammalian RNA demethylase that impacts RNA metabolism and mouse fertility. Mol Cell. 2013 Jan 10;49(1):18-29. doi: 10.1016/j.molcel.2012.10.015. Epub 2012 Nov 21.
Ref 355 Piperazine derivatives for treating disorders. US9695160.
Ref 356 Siltuximab. 2022 May 15. Drugs and Lactation Database (LactMed) [Internet]. Bethesda (MD): National Library of Medicine (US); 2006-.
Ref 357 National Cancer Institute Drug Dictionary (drug name MK1454).
Ref 358 Magnitude of Therapeutic STING Activation Determines CD8(+) T Cell-Mediated Anti-tumor Immunity. Cell Rep. 2018 Dec 11;25(11):3074-3085.e5. doi: 10.1016/j.celrep.2018.11.047.
Ref 359 E7766, a Macrocycle-Bridged Stimulator of Interferon Genes (STING) Agonist with Potent Pan-Genotypic Activity. ChemMedChem. 2021 Jun 7;16(11):1740-1743. doi: 10.1002/cmdc.202100068. Epub 2021 Feb 25.
Ref 360 Clinical pipeline report, company report or official report of ImmuneSensor Therapeutics.
Ref 361 National Cancer Institute Drug Dictionary (drug name ML2118).
Ref 362 National Cancer Institute Drug Dictionary (drug name TAK676).
Ref 363 Clinical pipeline report, company report or official report of Silicon Therapeutics.
Ref 364 National Cancer Institute Drug Dictionary (drug name GSK3745417).
Ref 365 Challenges and Opportunities in the Clinical Development of STING Agonists for Cancer Immunotherapy. J Clin Med. 2020 Oct 16;9(10):3323. doi: 10.3390/jcm9103323.
Ref 366 Immunotherapy with engineered bacteria by targeting the STING pathway for anti-tumor immunity. Nat Commun. 2020 Jun 1;11(1):2739. doi: 10.1038/s41467-020-16602-0.
Ref 367 Targeting STING with covalent small-molecule inhibitors. Nature. 2018 Jul;559(7713):269-273. doi: 10.1038/s41586-018-0287-8. Epub 2018 Jul 4.
Ref 368 Clinical pipeline report, company report or official report of F-star Therapeutics.
Ref 369 c-Jun N-terminal kinase inhibitors: a patent review (2010 - 2014). Expert Opin Ther Pat. 2015;25(8):849-72. doi: 10.1517/13543776.2015.1039984. Epub 2015 May 19.
Ref 370 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: 1496).
Ref 371 Discovery of a new class of 4-anilinopyrimidines as potent c-Jun N-terminal kinase inhibitors: Synthesis and SAR studies. Bioorg Med Chem Lett. 2007 Feb 1;17(3):668-72. doi: 10.1016/j.bmcl.2006.10.093. Epub 2006 Nov 2.
Ref 372 Discovery of potent, highly selective, and orally bioavailable pyridine carboxamide c-Jun NH2-terminal kinase inhibitors. J Med Chem. 2006 Jul 27;49(15):4455-8. doi: 10.1021/jm060465l.
Ref 373 Discovery of potent and selective covalent inhibitors of JNK. Chem Biol. 2012 Jan 27;19(1):140-54. doi: 10.1016/j.chembiol.2011.11.010.
Ref 374 Corchorusin-D directed apoptosis of K562 cells occurs through activation of mitochondrial and death receptor pathways and suppression of AKT/PKB pathway. Cell Physiol Biochem. 2012;30(4):915-26. doi: 10.1159/000341469. Epub 2012 Sep 12.
Ref 375 Aminopyridine-based c-Jun N-terminal kinase inhibitors with cellular activity and minimal cross-kinase activity. J Med Chem. 2006 Jun 15;49(12):3563-80. doi: 10.1021/jm060199b.
Ref 376 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: 2616).
Ref 377 Synthesis and structure-activity relationships of a novel and selective bone morphogenetic protein receptor (BMP) inhibitor derived from the pyrazolo[1.5-a]pyrimidine scaffold of dorsomorphin: the discovery of ML347 as an ALK2 versus ALK3 selective MLPCN probe. Bioorg Med Chem Lett. 2013 Jun 1;23(11):3248-52. doi: 10.1016/j.bmcl.2013.03.113. Epub 2013 Apr 11.
Ref 378 Amelioration of acute myocardial infarction injury through targeted ferritin nanocages loaded with an ALKBH5 inhibitor. Acta Biomater. 2022 Mar 1;140:481-491. doi: 10.1016/j.actbio.2021.11.041. Epub 2021 Dec 5.
Ref 379 Discovery and characterization of a novel inhibitor of matrix metalloprotease-13 that reduces cartilage damage in vivo without joint fibroplasia side effects. J Biol Chem. 2007 Sep 21;282(38):27781-91. doi: 10.1074/jbc.M703286200. Epub 2007 Jul 10.
Ref 380 Leukemogenic Chromatin Alterations Promote AML Leukemia Stem Cells via a KDM4C-ALKBH5-AXL Signaling Axis. Cell Stem Cell. 2020 Jul 2;27(1):81-97.e8. doi: 10.1016/j.stem.2020.04.001. Epub 2020 May 12.
Ref 381 Fragment-Based Discovery of Low-Micromolar ATAD2 Bromodomain Inhibitors. J Med Chem. 2015 Jul 23;58(14):5649-73. doi: 10.1021/acs.jmedchem.5b00772. Epub 2015 Jul 9.
Ref 382 Company report (Mirati Therapeutics: formerly MethylGene)
Ref 383 The E3 ligase Cbl-b and TAM receptors regulate cancer metastasis via natural killer cells. Nature. 2014 Mar 27;507(7493):508-12. doi: 10.1038/nature12998. Epub 2014 Feb 19.
Ref 384 Clinical pipeline report, company report or official report of Ono Pharmaceutical.
Ref 385 AXL Targeting Abrogates Autophagic Flux and Induces Immunogenic Cell Death in Drug-Resistant Cancer Cells. J Thorac Oncol. 2020 Jun;15(6):973-999. doi: 10.1016/j.jtho.2020.01.015. Epub 2020 Feb 1.
Ref 386 Enapotamab vedotin, an AXL-specific antibody-drug conjugate, shows preclinical antitumor activity in non-small cell lung cancer. JCI Insight. 2019 Nov 1;4(21):e128199. doi: 10.1172/jci.insight.128199.
Ref 387 National Cancer Institute Drug Dictionary (drug name RXDX106).
Ref 388 First-in-human phase I study of BPI-9016M, a dual MET/Axl inhibitor, in patients with non-small cell lung cancer. J Hematol Oncol. 2020 Jan 16;13(1):6. doi: 10.1186/s13045-019-0834-2.
Ref 389 A Potent and Selective Dual Inhibitor of AXL and MERTK Possesses Both Immunomodulatory and Tumor-Targeted Activity. Front Oncol. 2020 Dec 7;10:598477. doi: 10.3389/fonc.2020.598477. eCollection 2020.
Ref 390 National Cancer Institute Drug Dictionary (drug name PF-07265807).
Ref 391 AXL receptor tyrosine kinase as a promising anti-cancer approach: functions, molecular mechanisms and clinical applications. Mol Cancer. 2019 Nov 4;18(1):153. doi: 10.1186/s12943-019-1090-3.
Ref 392 MicroPET/CT Imaging of AXL Downregulation by HSP90 Inhibition in Triple-Negative Breast Cancer. Contrast Media Mol Imaging. 2017 May 14;2017:1686525. doi: 10.1155/2017/1686525. eCollection 2017.