General Information of the m6A Regulator (ID: REG00025)
Regulator Name YTH domain-containing family protein 3 (YTHDF3)
Synonyms
DF3
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Gene Name YTHDF3
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)
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Afatinib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [2]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Cetuximab through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [3]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Dacomitinib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [4]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Epidermal growth factor through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [5]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of HEGF through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [6]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Icotinib hydrochloride through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [7]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Lapatinib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [8]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Merimepodib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [9]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Necitumumab through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [10]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of NERATINIB MALEATE through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [11]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Nitroglycerin through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [9]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Panitumumab through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [12]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of SKI-758 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Vandetanib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [14]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AC0010 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [15]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Almonertinib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [16]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Amivantamab through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [17]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ASP1929 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [18]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of CO-1686 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of DE-766 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [19]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of EGF816 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of HKI-272 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [20]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Indium-111 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [21]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Rindopepimut through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [22]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of SYM-004 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [23]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Varlitinib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [24]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Zalutumumab through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [4]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ABT-414 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [3]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ABX-EGF through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [25]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AFM24 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [26]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ASP8273 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [27]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of BDTX-189 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [28]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of BMS-599626 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [2]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of BMS-690514 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [22]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of CART-EGFR through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [29]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of CetuGEX through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [30]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of CI-1033 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [31]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of CK-101 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [31]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Depatuxizumab through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [31]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of EGFR antisense DNA through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [31]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of EGFR CART through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [32]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of EMB-01 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [33]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of EMD 55900 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [34]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of HER1-VSSP vaccine through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [35]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of HM-78136B through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [36]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Matuzumab through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [37]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of MEHD-7945A through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [38]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Pelitinib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [39]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of RM-1929 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [40]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of SN-32793 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [41]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Sym013 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [42]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Sym015 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [32]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Tarloxotinib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [43]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of TT-100 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [44]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of VATALANIB through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [21]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ZN-e4 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [45]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AMG 595 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [46]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Anti-EGFR CAR T through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [47]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AP32788 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [48]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AST-1306 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [21]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of BCA101 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [49]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of BIBX-1382 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [50]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Cipatinib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [51]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of CLN-081 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [52]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of CUDC-101 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [53]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of D2C7 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [54]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of EGFR806-specific CAR T cell through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [55]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of IMGN289 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of JNJ-26483327 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [56]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of LY3164530 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [57]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of MCLA-158 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [58]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of MM-151 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [31]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of MR1-1 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [59]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of PF-05230907 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [32]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Pyrotinib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [60]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of S-222611 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of SI-B001 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [61]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of SYN004 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [32]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of 111In-hEGF through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [62]
(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 YTH domain-containing family protein 3 (YTHDF3) 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], [63]
(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 YTH domain-containing family protein 3 (YTHDF3) 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], [64]
(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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of (E)-5-(4-Hydroxybenzylidene)-1-phenethylhydantoin through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [65]
(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 YTH domain-containing family protein 3 (YTHDF3) 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], [63]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of 10-hydroxy-18-methoxybetaenone through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [63]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [66]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [67]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [63]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [63]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of 2-methoxy-4-(2-nitrovinyl)phenol through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [63]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [68]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [69]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [70]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [71]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [72]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [73]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [63]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [74]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of 4-(2-nitrovinyl)phenol through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [63]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [75]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [64]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [63]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [76]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [77]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [78]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of 4557W through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [79]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [80]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [81]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [78]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [78]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of 6,7-diethoxy-4-styrylquinazoline through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [78]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [78]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [78]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [82]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [71]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [71]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AFM-21 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AG 112 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [83]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AG 9 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AG-213 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [63]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AG-538 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [84]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AG1478 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [85]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AGT-2000 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AL-6802 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Anti-EGFR humanized mabs through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Anti-EGFR mab through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ARX-AHD through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [75]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Benzyl-quinazolin-4-yl-amine through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [76]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Bmab-200 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of BPIQ-I through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [86]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of CL-387785 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [77]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Cochliobolic acid through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [87]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of EDP-13 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of EGFR inhibitor through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [88]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Epitinib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of FHT-2107 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of GI-3000 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of HDS-029 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [89]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of HKI-9924129 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [90]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of HM-61713B through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of HTS-00213 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [71]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of HTS-02876 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [91]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of HTS-05058 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [68]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ICR 62 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [92]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of IPS-01003 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of LA22-radioimmunoconjugates through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of LAVENDUSTIN A through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [78]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of mabionHER2 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of MDP-01 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of MG-111 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [93]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of MT-062 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [94]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [95]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [96]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [84]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [92]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [66]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [64]
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 YTH domain-containing family protein 3 (YTHDF3) 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], [94]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of N4-(3-methylphenyl)-4,6-quinazolinediamine through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [68]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of NRC-2694 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ON-128 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [64]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of OSI-75 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [97]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of PD-0166326 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [65]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of PD-0173956 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [65]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of PD-158780 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [64]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of PD-168393 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [96]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of PD182905 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [41]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of PF 5208766 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [98]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of PP121 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [99]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of RG-50810 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [91]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of RM-6427 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Ro-4396686 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [68]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of RX-1792 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of SYM-011 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of TGF alpha through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Theliatinib through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [100]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of WHI-P154 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [82]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of WZ-3146 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [13]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AZD-9935 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [101]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AZD4769 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [2]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of CGP-52411 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [102]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of CGP-53353 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [41]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Heparin-EGF-like factor through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [103]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of PD-153035 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [104]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of PKI166 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [105]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of RG7160 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [106]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of TAK165 through regulating the expression of Epidermal growth factor receptor (EGFR). [1], [107]
Extracellular signal-regulated kinase 1 (ERK1)
ASTX029 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 1 (ERK1) is a therapeutic target for ASTX029. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ASTX029 through regulating the expression of Extracellular signal-regulated kinase 1 (ERK1). [108], [109]
BVD-523 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 1 (ERK1) is a therapeutic target for BVD-523. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of BVD-523 through regulating the expression of Extracellular signal-regulated kinase 1 (ERK1). [108], [110]
HH2710 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 1 (ERK1) is a therapeutic target for HH2710. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of HH2710 through regulating the expression of Extracellular signal-regulated kinase 1 (ERK1). [108], [111]
ASN007 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 1 (ERK1) is a therapeutic target for ASN007. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ASN007 through regulating the expression of Extracellular signal-regulated kinase 1 (ERK1). [108], [112]
GDC-0994 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 1 (ERK1) is a therapeutic target for GDC-0994. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of GDC-0994 through regulating the expression of Extracellular signal-regulated kinase 1 (ERK1). [31], [108]
JSI-1187 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 1 (ERK1) is a therapeutic target for JSI-1187. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of JSI-1187 through regulating the expression of Extracellular signal-regulated kinase 1 (ERK1). [108], [113]
VAN-10-4-eluting stent [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 1 (ERK1) is a therapeutic target for VAN-10-4-eluting stent. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of VAN-10-4-eluting stent through regulating the expression of Extracellular signal-regulated kinase 1 (ERK1). [108], [114]
COR-D [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 1 (ERK1) is a therapeutic target for COR-D. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of COR-D through regulating the expression of Extracellular signal-regulated kinase 1 (ERK1). [108], [115]
6-[(E)-2-(4-Fluoro-phenyl)-vinyl]-9H-purine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 1 (ERK1) is a therapeutic target for 6-[(E)-2-(4-Fluoro-phenyl)-vinyl]-9H-purine. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of 6-[(E)-2-(4-Fluoro-phenyl)-vinyl]-9H-purine through regulating the expression of Extracellular signal-regulated kinase 1 (ERK1). [108], [116]
Extracellular signal-regulated kinase 2 (ERK2)
ASTX029 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for ASTX029. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ASTX029 through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [108], [109]
BVD-523 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for BVD-523. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of BVD-523 through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [108], [117]
HH2710 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for HH2710. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of HH2710 through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [108], [111]
GDC-0994 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for GDC-0994. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of GDC-0994 through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [31], [108]
JSI-1187 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for JSI-1187. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of JSI-1187 through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [108], [113]
LY3214996 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for LY3214996. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of LY3214996 through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [108], [112]
VAN-10-4-eluting stent [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for VAN-10-4-eluting stent. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of VAN-10-4-eluting stent through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [108], [114]
COR-D [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for COR-D. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of COR-D through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [108], [118]
(4-Fluoro-phenyl)-(9-methyl-9H-purin-6-yl)-amine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for (4-Fluoro-phenyl)-(9-methyl-9H-purin-6-yl)-amine. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of (4-Fluoro-phenyl)-(9-methyl-9H-purin-6-yl)-amine through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [108], [119]
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 Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for 4,5,6,7-tetrabromo-1H-benzo[d][1,2,3]triazole. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of 4,5,6,7-tetrabromo-1H-benzo[d][1,2,3]triazole through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [108], [120]
AEZS-131 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for AEZS-131. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AEZS-131 through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [108], [121]
Bisindolylmaleimide-I [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for Bisindolylmaleimide-I. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Bisindolylmaleimide-I through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [108], [122]
BMS 536924 [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for BMS 536924. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of BMS 536924 through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [108], [123]
CI-1040 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for CI-1040. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of CI-1040 through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [108], [124]
DEBROMOHYMENIALDISINE [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for DEBROMOHYMENIALDISINE. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of DEBROMOHYMENIALDISINE through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [108], [119]
ERK inhibitor III [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for ERK inhibitor III. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ERK inhibitor III through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [108], [125]
FR-180204 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for FR-180204. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of FR-180204 through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [108], [126]
KN-62 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for KN-62. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of KN-62 through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [108], [127]
KT-5720 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for KT-5720. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of KT-5720 through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [108], [125]
Phosphonothreonine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for Phosphonothreonine. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Phosphonothreonine through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [108], [128]
RO-316233 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for RO-316233. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of RO-316233 through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [108], [119]
Ro-4396686 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for Ro-4396686. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Ro-4396686 through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [108], [119]
Ro31-8220 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for Ro31-8220. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Ro31-8220 through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [72], [108]
SCH772984 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for SCH772984. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of SCH772984 through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [108], [129]
SB220025 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Extracellular signal-regulated kinase 2 (ERK2) is a therapeutic target for SB220025. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of SB220025 through regulating the expression of Extracellular signal-regulated kinase 2 (ERK2). [108], [116]
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 YTH domain-containing family protein 3 (YTHDF3) 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). [130], [131]
Gap junction alpha-1 protein (GJA1)
Act1 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Gap junction alpha-1 protein (GJA1) is a therapeutic target for Act1. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Act1 through regulating the expression of Gap junction alpha-1 protein (GJA1). [1], [132]
Granexin gel [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Gap junction alpha-1 protein (GJA1) is a therapeutic target for Granexin gel. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Granexin gel through regulating the expression of Gap junction alpha-1 protein (GJA1). [1], [133]
HCB1019 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Gap junction alpha-1 protein (GJA1) is a therapeutic target for HCB1019. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of HCB1019 through regulating the expression of Gap junction alpha-1 protein (GJA1). [1], [134]
octanol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Gap junction alpha-1 protein (GJA1) is a therapeutic target for octanol. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of octanol through regulating the expression of Gap junction alpha-1 protein (GJA1). [1], [135]
Interleukin-1 beta (IL1B)
Canakinumab [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Interleukin-1 beta (IL1B) is a therapeutic target for Canakinumab. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Canakinumab through regulating the expression of Interleukin-1 beta (IL1B). [108], [136]
Diacerein [Phase 4]
In total 1 mechanisms lead to this potential drug response
Response Summary Interleukin-1 beta (IL1B) is a therapeutic target for Diacerein. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Diacerein through regulating the expression of Interleukin-1 beta (IL1B). [108], [137]
Gallium nitrate [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Interleukin-1 beta (IL1B) is a therapeutic target for Gallium nitrate. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Gallium nitrate through regulating the expression of Interleukin-1 beta (IL1B). [108], [138]
Glucosamine [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Interleukin-1 beta (IL1B) is a therapeutic target for Glucosamine. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Glucosamine through regulating the expression of Interleukin-1 beta (IL1B). [108], [139]
Rilonacept [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Interleukin-1 beta (IL1B) is a therapeutic target for Rilonacept. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Rilonacept through regulating the expression of Interleukin-1 beta (IL1B). [108], [140]
XOMA 052 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Interleukin-1 beta (IL1B) is a therapeutic target for XOMA 052. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of XOMA 052 through regulating the expression of Interleukin-1 beta (IL1B). [108], [141]
ABT-981 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Interleukin-1 beta (IL1B) is a therapeutic target for ABT-981. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ABT-981 through regulating the expression of Interleukin-1 beta (IL1B). [108], [142]
AC-201 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Interleukin-1 beta (IL1B) is a therapeutic target for AC-201. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AC-201 through regulating the expression of Interleukin-1 beta (IL1B). [108], [143]
LY-2189102 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Interleukin-1 beta (IL1B) is a therapeutic target for LY-2189102. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of LY-2189102 through regulating the expression of Interleukin-1 beta (IL1B). [108], [144]
CYT-013-IL1bQb [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Interleukin-1 beta (IL1B) is a therapeutic target for CYT-013-IL1bQb. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of CYT-013-IL1bQb through regulating the expression of Interleukin-1 beta (IL1B). [108], [145]
TT-301 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Interleukin-1 beta (IL1B) is a therapeutic target for TT-301. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of TT-301 through regulating the expression of Interleukin-1 beta (IL1B). [108], [146]
Celastrol [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Interleukin-1 beta (IL1B) is a therapeutic target for Celastrol. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Celastrol through regulating the expression of Interleukin-1 beta (IL1B). [108], [147]
DVD-Ig [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Interleukin-1 beta (IL1B) is a therapeutic target for DVD-Ig. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of DVD-Ig through regulating the expression of Interleukin-1 beta (IL1B). [108], [148]
CDP-484 [Discontinued in Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Interleukin-1 beta (IL1B) is a therapeutic target for CDP-484. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of CDP-484 through regulating the expression of Interleukin-1 beta (IL1B). [108], [149]
Lysine-specific demethylase 5B (KDM5B)
PBIT [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Lysine-specific demethylase 5B (KDM5B) is a therapeutic target for PBIT. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of PBIT through regulating the expression of Lysine-specific demethylase 5B (KDM5B). [150], [151]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AZD5363 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [31], [108]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Enzastaurin through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [152]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of GDC-0068 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [31], [108]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ARQ 092 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [153]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of CI-1033 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [31], [108]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of CMX-2043 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [2], [108]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of GSK2110183 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [154]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of PTX-200 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [31], [108]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of RX-0201 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [155]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Triciribine prodrug through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [55], [108]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ARQ 751 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [155]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of BMS-754807 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [156]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of M2698 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [31], [108]
(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 YTH domain-containing family protein 3 (YTHDF3) 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). [108], [119]
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 YTH domain-containing family protein 3 (YTHDF3) 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). [108], [120]
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 YTH domain-containing family protein 3 (YTHDF3) 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). [108], [119]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of A-443654 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [119]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of A-674563 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [157]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Akt inhibitor VIII through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [125]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ALM-301 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [158]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Bisindolylmaleimide-I through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [159]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of BMS 536924 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [119]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of BX-517 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [127]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of CI-1040 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [155]
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 YTH domain-containing family protein 3 (YTHDF3) 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). [108], [160]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of KN-62 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [159]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Lactoquinomycin through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [161]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of LD-101 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [155]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of MYRIOCIN through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [162]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of NU-1001-41 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [155]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of RO-316233 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [119]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Ro31-8220 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [163]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of SB-747651A through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [126]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of STAUROSPORINONE through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [162]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of VLI-27 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [108], [155]
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 YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Squalestatin 1 through regulating the expression of RAC-alpha serine/threonine-protein kinase (AKT1). [31], [108]
Stress-activated protein kinase 2a (p38 alpha)
Ozagrel [Phase 4]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for Ozagrel. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Ozagrel through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [164]
Losmapimod [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for Losmapimod. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Losmapimod through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [165]
Dilmapimod [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for Dilmapimod. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Dilmapimod through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [166]
VX-702 [Phase 2a]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for VX-702. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of VX-702 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [3], [108]
VX-745 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for VX-745. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of VX-745 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [167]
(5-amino-1-phenyl-1H-pyrazol-4-yl)phenylmethanone [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for (5-amino-1-phenyl-1H-pyrazol-4-yl)phenylmethanone. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of (5-amino-1-phenyl-1H-pyrazol-4-yl)phenylmethanone through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [168]
2-Chlorophenol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for 2-Chlorophenol. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of 2-Chlorophenol through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [169]
3-(1-NAPHTHYLMETHOXY)PYRIDIN-2-AMINE [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for 3-(1-NAPHTHYLMETHOXY)PYRIDIN-2-AMINE. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of 3-(1-NAPHTHYLMETHOXY)PYRIDIN-2-AMINE through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [125]
3-(Benzyloxy)Pyridin-2-Amine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for 3-(Benzyloxy)Pyridin-2-Amine. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of 3-(Benzyloxy)Pyridin-2-Amine through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [125]
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 2a (p38 alpha) is a therapeutic target for 4,5,6,7-tetrabromo-1H-benzo[d][1,2,3]triazole. The YTH domain-containing family protein 3 (YTHDF3) 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 2a (p38 alpha). [108], [170]
4-(2-Ethyl-4-m-tolyl-thiazol-5-yl)-pyridine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for 4-(2-Ethyl-4-m-tolyl-thiazol-5-yl)-pyridine. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of 4-(2-Ethyl-4-m-tolyl-thiazol-5-yl)-pyridine through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [171]
4-PHENOXY-N-(PYRIDIN-2-YLMETHYL)BENZAMIDE [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for 4-PHENOXY-N-(PYRIDIN-2-YLMETHYL)BENZAMIDE. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of 4-PHENOXY-N-(PYRIDIN-2-YLMETHYL)BENZAMIDE through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [169]
4-Phenylsulfanyl-7H-pyrrolo[2,3-d]pyrimidine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for 4-Phenylsulfanyl-7H-pyrrolo[2,3-d]pyrimidine. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of 4-Phenylsulfanyl-7H-pyrrolo[2,3-d]pyrimidine through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [123]
6-(4-Fluoro-phenylsulfanyl)-9H-purine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for 6-(4-Fluoro-phenylsulfanyl)-9H-purine. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of 6-(4-Fluoro-phenylsulfanyl)-9H-purine through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [123]
6-Benzylsulfanyl-9H-purine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for 6-Benzylsulfanyl-9H-purine. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of 6-Benzylsulfanyl-9H-purine through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [119]
6-o-tolylquinazolin-2-amine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for 6-o-tolylquinazolin-2-amine. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of 6-o-tolylquinazolin-2-amine through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [172]
6-Phenylsulfanyl-9H-purine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for 6-Phenylsulfanyl-9H-purine. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of 6-Phenylsulfanyl-9H-purine through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [123]
9-(4-Fluoro-benzyl)-6-phenylsulfanyl-9H-purine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for 9-(4-Fluoro-benzyl)-6-phenylsulfanyl-9H-purine. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of 9-(4-Fluoro-benzyl)-6-phenylsulfanyl-9H-purine through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [173]
9-Benzyl-6-(4-fluoro-phenylsulfanyl)-9H-purine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for 9-Benzyl-6-(4-fluoro-phenylsulfanyl)-9H-purine. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of 9-Benzyl-6-(4-fluoro-phenylsulfanyl)-9H-purine through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [123]
9-Benzyl-6-phenylsulfanyl-9H-purine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for 9-Benzyl-6-phenylsulfanyl-9H-purine. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of 9-Benzyl-6-phenylsulfanyl-9H-purine through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [123]
AG1478 [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for AG1478. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AG1478 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [174]
B-Octylglucoside [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for B-Octylglucoside. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of B-Octylglucoside through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [175]
Bisindolylmaleimide-I [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for Bisindolylmaleimide-I. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Bisindolylmaleimide-I through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [123]
CI-1040 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for CI-1040. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of CI-1040 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [176]
Dihydro-quinolinone [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for Dihydro-quinolinone. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Dihydro-quinolinone through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [177]
DP-802 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for DP-802. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of DP-802 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [164]
GSK-280 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for GSK-280. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of GSK-280 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [178]
GW-788388 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for GW-788388. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of GW-788388 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [119]
IN-1130 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for IN-1130. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of IN-1130 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [179]
IN-1166 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for IN-1166. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of IN-1166 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [127]
KN-62 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for KN-62. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of KN-62 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [177]
KT-5720 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for KT-5720. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of KT-5720 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [180]
L-779450 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for L-779450. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of L-779450 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [120]
ML-3163 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for ML-3163. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ML-3163 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [181]
ML-3375 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for ML-3375. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ML-3375 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [182]
ML-3403 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for ML-3403. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ML-3403 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [119]
N-(3-(trifluoromethoxy)benzyl)-4-phenoxybenzamide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for N-(3-(trifluoromethoxy)benzyl)-4-phenoxybenzamide. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of N-(3-(trifluoromethoxy)benzyl)-4-phenoxybenzamide through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [183]
N-(3-(trifluoromethyl)benzyl)-4-phenoxybenzamide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for N-(3-(trifluoromethyl)benzyl)-4-phenoxybenzamide. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of N-(3-(trifluoromethyl)benzyl)-4-phenoxybenzamide through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [183]
N-(4-(trifluoromethyl)benzyl)-4-phenoxybenzamide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for N-(4-(trifluoromethyl)benzyl)-4-phenoxybenzamide. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of N-(4-(trifluoromethyl)benzyl)-4-phenoxybenzamide through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [183]
N-(4-fluorobenzyl)-N-(pyridin-4-yl)-2-naphthamide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for N-(4-fluorobenzyl)-N-(pyridin-4-yl)-2-naphthamide. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of N-(4-fluorobenzyl)-N-(pyridin-4-yl)-2-naphthamide through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [119]
N-(4-methyl-benzyl)-4-phenoxy-benzamide [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for N-(4-methyl-benzyl)-4-phenoxy-benzamide. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of N-(4-methyl-benzyl)-4-phenoxy-benzamide through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [184]
Oxindole 94 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for Oxindole 94. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Oxindole 94 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [183]
PD-0166326 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for PD-0166326. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of PD-0166326 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [185]
PD-0173956 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for PD-0173956. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of PD-0173956 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [172]
PHA-666859 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for PHA-666859. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of PHA-666859 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [164]
Phenyl-(3-phenyl-1H-indazol-6-yl)-amine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for Phenyl-(3-phenyl-1H-indazol-6-yl)-amine. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Phenyl-(3-phenyl-1H-indazol-6-yl)-amine through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [119]
RO-316233 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for RO-316233. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of RO-316233 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [123]
Ro-3201195 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for Ro-3201195. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Ro-3201195 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [186]
Ro31-8220 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for Ro31-8220. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Ro31-8220 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [185]
RWJ-68354 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for RWJ-68354. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of RWJ-68354 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [181]
SB-216995 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for SB-216995. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of SB-216995 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [187]
SB-218655 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for SB-218655. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of SB-218655 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [172]
SB-227931 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for SB-227931. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of SB-227931 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [188]
Small molecule 34 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for Small molecule 34. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Small molecule 34 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [125]
STAUROSPORINONE [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for STAUROSPORINONE. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of STAUROSPORINONE through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [119]
Talmapimod [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for Talmapimod. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Talmapimod through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [169]
Triazolopyridine [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for Triazolopyridine. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Triazolopyridine through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [169]
UCB-1277763 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for UCB-1277763. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of UCB-1277763 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [164]
ZM-336372 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for ZM-336372. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ZM-336372 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [189]
FR167653 [Discontinued in Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for FR167653. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of FR167653 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [3], [108]
PAMAPIMOD [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for PAMAPIMOD. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of PAMAPIMOD through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [3], [108]
R-1487 [Discontinued in Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for R-1487. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of R-1487 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [166]
SB 203580 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for SB 203580. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of SB 203580 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [190]
SB 235699 [Discontinued in Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for SB 235699. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of SB 235699 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [191]
SB-242235 [Discontinued in Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for SB-242235. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of SB-242235 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [192]
SB220025 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for SB220025. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of SB220025 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [193]
SC-102 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Stress-activated protein kinase 2a (p38 alpha) is a therapeutic target for SC-102. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of SC-102 through regulating the expression of Stress-activated protein kinase 2a (p38 alpha). [108], [125]
Tumor necrosis factor (TNF)
Adalimumab [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Adalimumab. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Adalimumab through regulating the expression of Tumor necrosis factor (TNF). [108], [194]
Certolizumab [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Certolizumab. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Certolizumab through regulating the expression of Tumor necrosis factor (TNF). [108], [195]
Enbrel [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Enbrel. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Enbrel through regulating the expression of Tumor necrosis factor (TNF). [108], [196]
Etanercept [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Etanercept. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Etanercept through regulating the expression of Tumor necrosis factor (TNF). [108], [197]
Golimumab [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Golimumab. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Golimumab through regulating the expression of Tumor necrosis factor (TNF). [108], [198]
Infliximab [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Infliximab. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Infliximab through regulating the expression of Tumor necrosis factor (TNF). [108], [199]
Lenalidomide [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Lenalidomide. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Lenalidomide through regulating the expression of Tumor necrosis factor (TNF). [108], [139]
Nafamostat [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Nafamostat. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Nafamostat through regulating the expression of Tumor necrosis factor (TNF). [108], [200]
Pentoxifylline [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Pentoxifylline. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Pentoxifylline through regulating the expression of Tumor necrosis factor (TNF). [108], [201]
Thalidomide [Approved]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Thalidomide. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Thalidomide through regulating the expression of Tumor necrosis factor (TNF). [108], [202]
ABP 501 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for ABP 501. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ABP 501 through regulating the expression of Tumor necrosis factor (TNF). [108], [203]
CPL-7075 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for CPL-7075. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of CPL-7075 through regulating the expression of Tumor necrosis factor (TNF). [108], [204]
Golnerminogene pradenovac [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Golnerminogene pradenovac. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Golnerminogene pradenovac through regulating the expression of Tumor necrosis factor (TNF). [108], [205]
PF-06410293 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for PF-06410293. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of PF-06410293 through regulating the expression of Tumor necrosis factor (TNF). [108], [206]
PF-06438179 [Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for PF-06438179. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of PF-06438179 through regulating the expression of Tumor necrosis factor (TNF). [108], [207]
ABT-122 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for ABT-122. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ABT-122 through regulating the expression of Tumor necrosis factor (TNF). [108], [208]
AN0128 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for AN0128. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AN0128 through regulating the expression of Tumor necrosis factor (TNF). [108], [209]
AP-301-IH [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for AP-301-IH. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AP-301-IH through regulating the expression of Tumor necrosis factor (TNF). [108], [210]
ART621 [Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for ART621. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ART621 through regulating the expression of Tumor necrosis factor (TNF). [53], [108]
BAICALEIN [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for BAICALEIN. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of BAICALEIN through regulating the expression of Tumor necrosis factor (TNF). [108], [211]
COVA322 [Phase 1/2a]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for COVA322. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of COVA322 through regulating the expression of Tumor necrosis factor (TNF). [108], [212]
DLX-105 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for DLX-105. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of DLX-105 through regulating the expression of Tumor necrosis factor (TNF). [108], [213]
ESBA-105 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for ESBA-105. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ESBA-105 through regulating the expression of Tumor necrosis factor (TNF). [108], [214]
Ortataxel [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Ortataxel. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Ortataxel through regulating the expression of Tumor necrosis factor (TNF). [108], [215]
Pegsunercept [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Pegsunercept. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Pegsunercept through regulating the expression of Tumor necrosis factor (TNF). [108], [216]
RDP58 [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for RDP58. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of RDP58 through regulating the expression of Tumor necrosis factor (TNF). [108], [217]
TNF alpha kinoid [Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for TNF alpha kinoid. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of TNF alpha kinoid through regulating the expression of Tumor necrosis factor (TNF). [108], [218]
ABBV-257 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for ABBV-257. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ABBV-257 through regulating the expression of Tumor necrosis factor (TNF). [108], [219]
AST-005 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for AST-005. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AST-005 through regulating the expression of Tumor necrosis factor (TNF). [108], [220]
AVX-470 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for AVX-470. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AVX-470 through regulating the expression of Tumor necrosis factor (TNF). [108], [220]
CYT-609 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for CYT-609. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of CYT-609 through regulating the expression of Tumor necrosis factor (TNF). [108], [221]
INB03 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for INB03. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of INB03 through regulating the expression of Tumor necrosis factor (TNF). [108], [222]
PF-05230905 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for PF-05230905. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of PF-05230905 through regulating the expression of Tumor necrosis factor (TNF). [108], [223]
PMI-005 [Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for PMI-005. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of PMI-005 through regulating the expression of Tumor necrosis factor (TNF). [108], [224]
ABX-0401 [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for ABX-0401. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ABX-0401 through regulating the expression of Tumor necrosis factor (TNF). [108], [148]
Celastrol [Preclinical]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Celastrol. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Celastrol through regulating the expression of Tumor necrosis factor (TNF). [21], [108]
2-Propanol, Isopropanol [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for 2-Propanol, Isopropanol. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of 2-Propanol, Isopropanol through regulating the expression of Tumor necrosis factor (TNF). [108], [225]
DOM-0215 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for DOM-0215. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of DOM-0215 through regulating the expression of Tumor necrosis factor (TNF). [108], [226]
IK-862 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for IK-862. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of IK-862 through regulating the expression of Tumor necrosis factor (TNF). [108], [227]
PKF-241-466 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for PKF-241-466. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of PKF-241-466 through regulating the expression of Tumor necrosis factor (TNF). [108], [227]
PKF-242-484 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for PKF-242-484. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of PKF-242-484 through regulating the expression of Tumor necrosis factor (TNF). [108], [228]
Y-39041 [Investigative]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Y-39041. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Y-39041 through regulating the expression of Tumor necrosis factor (TNF). [108], [229]
ALS-00T2-0501 [Discontinued in Phase 1]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for ALS-00T2-0501. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ALS-00T2-0501 through regulating the expression of Tumor necrosis factor (TNF). [108], [230]
AME-527 [Discontinued in Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for AME-527. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of AME-527 through regulating the expression of Tumor necrosis factor (TNF). [108], [226]
Camobucol [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Camobucol. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Camobucol through regulating the expression of Tumor necrosis factor (TNF). [108], [231]
CDP571 [Discontinued in Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for CDP571. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of CDP571 through regulating the expression of Tumor necrosis factor (TNF). [108], [232]
CRx-191 [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for CRx-191. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of CRx-191 through regulating the expression of Tumor necrosis factor (TNF). [108], [233]
CYT-007-TNFQb [Discontinued in Phase 1/2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for CYT-007-TNFQb. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of CYT-007-TNFQb through regulating the expression of Tumor necrosis factor (TNF). [108], [234]
FR-133605 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for FR-133605. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of FR-133605 through regulating the expression of Tumor necrosis factor (TNF). [108], [235]
ISIS 104838 [Discontinued in Phase 2]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for ISIS 104838. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of ISIS 104838 through regulating the expression of Tumor necrosis factor (TNF). [108], [236]
MDL-201112 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for MDL-201112. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of MDL-201112 through regulating the expression of Tumor necrosis factor (TNF). [108], [237]
PNU-282987 [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for PNU-282987. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of PNU-282987 through regulating the expression of Tumor necrosis factor (TNF). [108], [238]
Segard [Discontinued in Phase 3]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for Segard. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of Segard through regulating the expression of Tumor necrosis factor (TNF). [108], [239]
TNFQb therapeutic vaccines [Terminated]
In total 1 mechanisms lead to this potential drug response
Response Summary Tumor necrosis factor (TNF) is a therapeutic target for TNFQb therapeutic vaccines. The YTH domain-containing family protein 3 (YTHDF3) has potential in affecting the response of TNFQb therapeutic vaccines through regulating the expression of Tumor necrosis factor (TNF). [108], [240]
References
Ref 1 YTHDF3 Induces the Translation of m(6)A-Enriched Gene Transcripts to Promote Breast Cancer Brain Metastasis. Cancer Cell. 2020 Dec 14;38(6):857-871.e7. doi: 10.1016/j.ccell.2020.10.004. Epub 2020 Oct 29.
Ref 2 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 3 Clinical pipeline report, company report or official report of GlaxoSmithKline (2009).
Ref 4 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 5 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 6 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 7 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 8 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 9 Emerging drugs for diabetic foot ulcers. Expert Opin Emerg Drugs. 2006 Nov;11(4):709-24. doi: 10.1517/14728214.11.4.709.
Ref 10 Boehringer Ingelheim. Product Development Pipeline. June 2 2009.
Ref 11 Nasopharyngeal carcinoma: Current treatment options and future directions. J Nasopharyng Carcinoma, 2014, 1(16): e16.
Ref 12 Quantitative prediction of fold resistance for inhibitors of EGFR. Biochemistry. 2009 Sep 8;48(35):8435-48. doi: 10.1021/bi900729a.
Ref 13 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 14 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 15 Clinical pipeline report, company report or official report of Ionis Pharmaceuticals.
Ref 16 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 17 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 18 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 19 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 20 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 21 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 22 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 23 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 24 Clinical pipeline report, company report or official report of Roche (2009).
Ref 25 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 26 Marine-Sourced Anti-Cancer and Cancer Pain Control Agents in Clinical and Late Preclinical Development. Mar Drugs. 2014 January; 12(1): 255-278.
Ref 27 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 28 Clinical pipeline report, company report or official report of EpimAb Biotherapeutics.
Ref 29 ClinicalTrials.gov (NCT03152435) EGFR CART Cells for Patients With Metastatic Colorectal Cancer
Ref 30 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 31 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
Ref 32 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
Ref 33 Clinical pipeline report, company report or official report of Zentalis Pharmaceuticals.
Ref 34 ClinicalTrials.gov (NCT01869166) Treatment of Chemotherapy Refractory EGFR(Epidermal Growth Factor Receptor) Positive Advanced Solid Tumors (CART-EGFR)
Ref 35 BiPar Sciences Co-founder Reunites Management Team At TriAct Therapeutics to Advance Clinical Stage Cancer Programs. TriAct Therapeutics. Sept. 10, 2009.
Ref 36 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 37 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 38 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 39 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 40 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 41 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 42 Clinical pipeline report, company report or official report of Black Diamond Therapeutics.
Ref 43 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 44 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 45 Clinical pipeline report, company report or official report of Affimed Therapeutics.
Ref 46 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 47 ClinicalTrials.gov (NCT03638167) EGFR806-specific CAR T Cell Locoregional Immunotherapy for EGFR-positive Recurrent or Refractory Pediatric CNS Tumors
Ref 48 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 49 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 50 World Antibody-Drug Conjugate Summit, October 15-16, 2013, San Francisco, CA. MAbs. 2014 January 1; 6(1): 18-29.
Ref 51 Company report (Biooncology)
Ref 52 Clinical pipeline report, company report or official report of SystImmune.
Ref 53 Bispecific antibodies rise again. Nat Rev Drug Discov. 2014 Nov;13(11):799-801. doi: 10.1038/nrd4478.
Ref 54 Clinical pipeline report, company report or official report of Merus.
Ref 55 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
Ref 56 ClinicalTrials.gov (NCT02331693) CAR T Cells in Treating Patients With Malignant Gliomas Overexpressing EGFR
Ref 57 National Cancer Institute Drug Dictionary (drug id 596693).
Ref 58 Clinical pipeline report, company report or official report of Shionogi (2011).
Ref 59 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 60 Antitumor Effects of EGFR Antisense Guanidine-Based Peptide Nucleic Acids in Cancer Models. ACS Chem Biol. 2013 February 15; 8(2): 345-352.
Ref 61 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 62 Clinical pipeline report, company report or official report of Bristol-Myers Squibb.
Ref 63 Protein-tyrosine kinase inhibition: mechanism-based discovery of antitumor agents. J Nat Prod. 1992 Nov;55(11):1529-60. doi: 10.1021/np50089a001.
Ref 64 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 65 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 66 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 67 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 68 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 69 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 70 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 71 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 72 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 73 Novel antiproliferative agents derived from lavendustin A. J Med Chem. 1994 Nov 25;37(24):4079-84. doi: 10.1021/jm00050a005.
Ref 74 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 75 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 76 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 77 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 78 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 79 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 80 Selected novel anticancer treatments targeting cell signaling proteins. Oncologist. 2001;6(6):517-37. doi: 10.1634/theoncologist.6-6-517.
Ref 81 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 82 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 83 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 84 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 85 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 86 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 87 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 88 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 89 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 90 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 91 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 92 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 93 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 94 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 95 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 96 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 97 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 98 Effects of hEGF (MG111) on gastric mucosal potential difference in rats. Scand J Gastroenterol Suppl. 1989;162:198-201. doi: 10.3109/00365528909091160.
Ref 99 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 100 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 101 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 102 WO patent application no. 2009,0582,67, Benzomorpholine derivatives and methods of use.
Ref 103 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 104 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 105 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 106 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 107 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 108 N6-methyladenosine reader YTH N6-methyladenosine RNA binding protein 3 or insulin like growth factor 2 mRNA binding protein 2 knockdown protects human bronchial epithelial cells from hypoxia/reoxygenation injury by inactivating p38 MAPK, AKT, ERK1/2, and NF-KappaB pathways. Bioengineered. 2022 May;13(5):11973-11986. doi: 10.1080/21655979.2021.1999550.
Ref 109 DOI: 10.1158/1538-7445.AM2015-4693
Ref 110 US patent application no. 7,425,545, Modulation of C-reactive protein expression.
Ref 111 Clinical pipeline report, company report or official report of Astex Pharmaceuticals.
Ref 112 National Cancer Institute Drug Dictionary (drug name JSI1187).
Ref 113 Clinical pipeline report, company report or official report of HaiHe Biopharma.
Ref 114 ERK Mutations Confer Resistance to Mitogen-Activated Protein Kinase Pathway Inhibitors
Ref 115 WO patent application no. 2013,1850,32, Nanotherapeutics for drug targeting.
Ref 116 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 117 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: 1804).
Ref 118 Selective glycogen synthase kinase 3 inhibitors potentiate insulin activation of glucose transport and utilization in vitro and in vivo. Diabetes. 2003 Mar;52(3):588-95. doi: 10.2337/diabetes.52.3.588.
Ref 119 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 120 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 121 Discovery of a novel ERK inhibitor with activity in models of acquired resistance to BRAF and MEK inhibitors. Cancer Discov. 2013 Jul;3(7):742-50. doi: 10.1158/2159-8290.CD-13-0070. Epub 2013 Apr 24.
Ref 122 Potent inhibition of checkpoint kinase activity by a hymenialdisine-derived indoloazepine. Bioorg Med Chem Lett. 2004 Aug 16;14(16):4319-21. doi: 10.1016/j.bmcl.2004.05.079.
Ref 123 Synthesis and biological testing of purine derivatives as potential ATP-competitive kinase inhibitors. J Med Chem. 2005 Feb 10;48(3):710-22. doi: 10.1021/jm0408767.
Ref 124 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: 1495).
Ref 125 How many drug targets are there Nat Rev Drug Discov. 2006 Dec;5(12):993-6.
Ref 126 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 127 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 128 Crystal structure of human ERK2 complexed with a pyrazolo[3,4-c]pyridazine derivative. Bioorg Med Chem Lett. 2006 Jan 1;16(1):55-8. doi: 10.1016/j.bmcl.2005.09.055. Epub 2005 Oct 18.
Ref 129 Characterization of ATP-independent ERK inhibitors identified through in silico analysis of the active ERK2 structure. Bioorg Med Chem Lett. 2006 Dec 15;16(24):6281-7. doi: 10.1016/j.bmcl.2006.09.038. Epub 2006 Sep 26.
Ref 130 m(6)A reader Ythdf3 protects hematopoietic stem cell integrity under stress by promoting the translation of Foxm1 and Asxl1 transcripts. Haematologica. 2022 Aug 1;107(8):1922-1927. doi: 10.3324/haematol.2021.279300.
Ref 131 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 132 Antibodies and venom peptides: new modalities for ion channels. Nat Rev Drug Discov. 2019 May;18(5):339-357. doi: 10.1038/s41573-019-0013-8.
Ref 133 Company report (OncoMed Pharmaceuticals)
Ref 134 Company report (FirstString Research)
Ref 135 Clinical pipeline report, company report or official report of OcuNexus Therapeutics.
Ref 136 2008 FDA drug approvals. Nat Rev Drug Discov. 2009 Feb;8(2):93-6. doi: 10.1038/nrd2813.
Ref 137 Small-molecule inhibitor of USP7/HAUSP ubiquitin protease stabilizes and activates p53 in cells. Mol Cancer Ther. 2009 Aug;8(8):2286-95. doi: 10.1158/1535-7163.MCT-09-0097. Epub 2009 Aug 11.
Ref 138 Glucosamine inhibits IL-1beta-mediated IL-8 production in prostate cancer cells by MAPK attenuation. J Cell Biochem. 2009 Oct 1;108(2):489-98. doi: 10.1002/jcb.22278.
Ref 139 2009 FDA drug approvals. Nat Rev Drug Discov. 2010 Feb;9(2):89-92. doi: 10.1038/nrd3101.
Ref 140 [Non-surgical treatment of osteoarthritis of large joints - new aspects]. Wien Med Wochenschr. 2009;159(3-4):76-86. doi: 10.1007/s10354-008-0603-2.
Ref 141 Elimination of arthritis pain and inflammation for over 2 years with a single 90 min, topical 14% gallium nitrate treatment: case reports and review of actions of gallium III. Med Hypotheses. 2005;65(6):1136-41. doi: 10.1016/j.mehy.2005.06.021. Epub 2005 Aug 24.
Ref 142 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
Ref 143 Gevokizumab, an anti-IL-1Beta mAb for the potential treatment of type 1 and 2 diabetes, rheumatoid arthritis and cardiovascular disease. Curr Opin Mol Ther. 2010 Dec;12(6):755-69.
Ref 144 Generation and characterization of ABT-981, a dual variable domain immunoglobulin (DVD-Ig(TM)) molecule that specifically and potently neutralizes both IL-1Alpha and IL-1Beta. MAbs. 2015;7(3):605-19. doi: 10.1080/19420862.2015.1026501.
Ref 145 A Swell in the Armamentarium of Antiepileptic Drug Targets. Epilepsy Curr. 2011 Nov-Dec; 11(6): 172-176.
Ref 146 Double-blind, randomized study evaluating the glycemic and anti-inflammatory effects of subcutaneous LY2189102, a neutralizing IL-1Beta antibody, in patients with type 2 diabetes. Diabetes Care. 2013 Aug;36(8):2239-46. doi: 10.2337/dc12-1835. Epub 2013 Mar 20.
Ref 147 Biological targets for therapeutic interventions in COPD: clinical potential. Int J Chron Obstruct Pulmon Dis. 2006 September; 1(3): 321-334.
Ref 148 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 149 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: 2623).
Ref 150 KDM5B promotes self-renewal of hepatocellular carcinoma cells through the microRNA-448-mediated YTHDF3/ITGA6 axis. J Cell Mol Med. 2021 Apr 7;25(13):5949-62. doi: 10.1111/jcmm.16342. Online ahead of print.
Ref 151 Clinical pipeline report, company report or official report of ISIS Pharmaceuticals (2009).
Ref 152 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 153 CenterWatch. Drugs in Clinical Trials Database. CenterWatch. 2008.
Ref 154 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 155 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 156 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 157 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 158 Comprehensive analysis of kinase inhibitor selectivity. Nat Biotechnol. 2011 Oct 30;29(11):1046-51. doi: 10.1038/nbt.1990.
Ref 159 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 160 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 161 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 162 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 163 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 164 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: 1499).
Ref 165 The p38 mitogen-activated protein kinase pathway plays a critical role in thrombin-induced endothelial chemokine production and leukocyte recruitment. Blood. 2001 Aug 1;98(3):667-73. doi: 10.1182/blood.v98.3.667.
Ref 166 Pharmacological inhibitors of MAPK pathways. Trends Pharmacol Sci. 2002 Jan;23(1):40-5. doi: 10.1016/s0165-6147(00)01865-4.
Ref 167 Efficacy, pharmacodynamics, and safety of VX-702, a novel p38 MAPK inhibitor, in rheumatoid arthritis: results of two randomized, double-blind, placebo-controlled clinical studies. Arthritis Rheum. 2009 May;60(5):1232-41. doi: 10.1002/art.24485.
Ref 168 Microwave-assisted synthesis of 5-aminopyrazol-4-yl ketones and the p38(MAPK) inhibitor RO3201195 for study in Werner syndrome cells. Bioorg Med Chem Lett. 2008 Jul 1;18(13):3745-8. doi: 10.1016/j.bmcl.2008.05.037. Epub 2008 May 16.
Ref 169 The Protein Data Bank. Nucleic Acids Res. 2000 Jan 1;28(1):235-42. doi: 10.1093/nar/28.1.235.
Ref 170 Discovery of aminoquinazolines as potent, orally bioavailable inhibitors of Lck: synthesis, SAR, and in vivo anti-inflammatory activity. J Med Chem. 2006 Sep 21;49(19):5671-86. doi: 10.1021/jm0605482.
Ref 171 Novel, potent and selective anilinoquinazoline and anilinopyrimidine inhibitors of p38 MAP kinase. Bioorg Med Chem Lett. 2004 Nov 1;14(21):5389-94. doi: 10.1016/j.bmcl.2004.08.007.
Ref 172 In silico search for multi-target anti-inflammatories in Chinese herbs and formulas. Bioorg Med Chem. 2010 Mar 15;18(6):2204-2218. doi: 10.1016/j.bmc.2010.01.070. Epub 2010 Feb 8.
Ref 173 Imidazopyrimidines, potent inhibitors of p38 MAP kinase. Bioorg Med Chem Lett. 2003 Feb 10;13(3):347-50. doi: 10.1016/s0960-894x(02)01020-x.
Ref 174 The neuroprotective action of JNK3 inhibitors based on the 6,7-dihydro-5H-pyrrolo[1,2-a]imidazole scaffold. Bioorg Med Chem Lett. 2005 Nov 1;15(21):4666-70. doi: 10.1016/j.bmcl.2005.07.076.
Ref 175 Inhibition of p38 MAPK decreases myocardial TNF-alpha expression and improves myocardial function and survival in endotoxemia. Cardiovasc Res. 2003 Oct 1;59(4):893-900. doi: 10.1016/s0008-6363(03)00509-1.
Ref 176 Prevention of the onset and progression of collagen-induced arthritis in rats by the potent p38 mitogen-activated protein kinase inhibitor FR167653. Arthritis Rheum. 2003 Sep;48(9):2670-81. doi: 10.1002/art.11227.
Ref 177 Synthesis and biological evaluation of trisubstituted imidazole derivatives as inhibitors of p38alpha mitogen-activated protein kinase. Bioorg Med Chem Lett. 2008 Jul 15;18(14):4006-10. doi: 10.1016/j.bmcl.2008.06.007. Epub 2008 Jun 6.
Ref 178 Novel triazolopyridylbenzamides as potent and selective p38Alpha inhibitors. Bioorg Med Chem Lett. 2012 May 15;22(10):3431-6. doi: 10.1016/j.bmcl.2012.03.099. Epub 2012 Apr 4.
Ref 179 Amide-based inhibitors of p38alpha MAP kinase. Part 2: design, synthesis and SAR of potent N-pyrimidyl amides. Bioorg Med Chem Lett. 2010 Apr 15;20(8):2560-3. doi: 10.1016/j.bmcl.2010.02.090. Epub 2010 Mar 2.
Ref 180 Mitogen-activated protein kinases in innate immunity. Nat Rev Immunol. 2013 Sep;13(9):679-92. doi: 10.1038/nri3495. Epub 2013 Aug 19.
Ref 181 Novel substituted pyridinyl imidazoles as potent anticytokine agents with low activity against hepatic cytochrome P450 enzymes. J Med Chem. 2003 Jul 17;46(15):3230-44. doi: 10.1021/jm030766k.
Ref 182 From imidazoles to pyrimidines: new inhibitors of cytokine release. J Med Chem. 2002 Jun 20;45(13):2733-40. doi: 10.1021/jm011098a.
Ref 183 Two classes of p38alpha MAP kinase inhibitors having a common diphenylether core but exhibiting divergent binding modes. Bioorg Med Chem Lett. 2005 Dec 1;15(23):5274-9. doi: 10.1016/j.bmcl.2005.08.038. Epub 2005 Sep 19.
Ref 184 A novel series of p38 MAP kinase inhibitors for the potential treatment of rheumatoid arthritis. Bioorg Med Chem Lett. 2004 Nov 1;14(21):5383-7. doi: 10.1016/j.bmcl.2004.08.006.
Ref 185 Structure-activity relationships of 6-(2,6-dichlorophenyl)-8-methyl-2-(phenylamino)pyrido[2,3-d]pyrimidin-7-ones: toward selective Abl inhibitors. Bioorg Med Chem Lett. 2009 Dec 15;19(24):6872-6. doi: 10.1016/j.bmcl.2009.10.085. Epub 2009 Oct 23.
Ref 186 The identification of potent and selective imidazole-based inhibitors of B-Raf kinase. Bioorg Med Chem Lett. 2006 Jan 15;16(2):378-81. doi: 10.1016/j.bmcl.2005.09.072. Epub 2005 Nov 2.
Ref 187 Discovery of S-[5-amino-1-(4-fluorophenyl)-1H-pyrazol-4-yl]-[3-(2,3-dihydroxypropoxy)phenyl]methanone (RO3201195), an orally bioavailable and highly selective inhibitor of p38 MAP kinase. J Med Chem. 2006 Mar 9;49(5):1562-75. doi: 10.1021/jm050736c.
Ref 188 Design and synthesis of 6-anilinoindazoles as selective inhibitors of c-Jun N-terminal kinase-3. Bioorg Med Chem Lett. 2005 Nov 15;15(22):5095-9. doi: 10.1016/j.bmcl.2005.06.083.
Ref 189 Novel inhibitor of p38 MAP kinase as an anti-TNF-alpha drug: discovery of N-[4-[2-ethyl-4-(3-methylphenyl)-1,3-thiazol-5-yl]-2-pyridyl]benzamide (TAK-715) as a potent and orally active anti-rheumatoid arthritis agent. J Med Chem. 2005 Sep 22;48(19):5966-79. doi: 10.1021/jm050165o.
Ref 190 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 191 Biphenyl amide p38 kinase inhibitors 4: DFG-in and DFG-out binding modes. Bioorg Med Chem Lett. 2008 Aug 1;18(15):4433-7. doi: 10.1016/j.bmcl.2008.06.028. Epub 2008 Jun 12.
Ref 192 Selective p38alpha inhibitors clinically evaluated for the treatment of chronic inflammatory disorders. J Med Chem. 2010 Mar 25;53(6):2345-53. doi: 10.1021/jm9012906.
Ref 193 Discovery of 6-(2,4-difluorophenoxy)-2-[3-hydroxy-1-(2-hydroxyethyl)propylamino]-8-methyl-8H-pyrido[2,3-d]pyrimidin-7-one (pamapimod) and 6-(2,4-difluorophenoxy)-8-methyl-2-(tetrahydro-2H-pyran-4-ylamino)pyrido[2,3-d]pyrimidin-7(8H)-one (R1487) as orally bioavailable and highly selective inhibitors of p38Alpha mitogen-activated protein kinase. J Med Chem. 2011 Apr 14;54(7):2255-65. doi: 10.1021/jm101423y. Epub 2011 Mar 4.
Ref 194 Targeted therapies in myelodysplastic syndromes: ASH 2003 review. Semin Hematol. 2004 Apr;41(2 Suppl 4):13-20. doi: 10.1053/j.seminhematol.2004.02.003.
Ref 195 Thalidomide and thalidomide analogues for maintenance of remission in Crohn's disease. Cochrane Database Syst Rev. 2009 Apr 15;2009(2):CD007351. doi: 10.1002/14651858.CD007351.pub2.
Ref 196 The potential of biologics for the treatment of asthma. Nat Rev Drug Discov. 2012 Dec;11(12):958-72. doi: 10.1038/nrd3792.
Ref 197 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2019
Ref 198 Oral pentoxifylline inhibits release of tumor necrosis factor-alpha from human peripheral blood monocytes : a potential treatment for aseptic loosening of total joint components. J Bone Joint Surg Am. 2001 Jul;83(7):1057-61. doi: 10.2106/00004623-200107000-00012.
Ref 199 [Efficacy of different thalidomide regimens for patients with multiple myeloma and its relationship with TNF-alpha level]. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2008 Dec;16(6):1312-5.
Ref 200 Emerging drugs for rheumatoid arthritis. Expert Opin Emerg Drugs. 2008 Mar;13(1):175-96. doi: 10.1517/14728214.13.1.175.
Ref 201 Drug insight: tumor necrosis factor-converting enzyme as a pharmaceutical target for rheumatoid arthritis. Nat Clin Pract Rheumatol. 2008 Jun;4(6):300-9. doi: 10.1038/ncprheum0797. Epub 2008 Apr 15.
Ref 202 Clinical pipeline report, company report or official report of AstraZeneca (2009).
Ref 203 Apoptosis and the FLIP and NF-kappa B proteins as pharmacodynamic criteria for biosimilar TNF-alpha antagonists. Biologics. 2014 Jul 31;8:211-20. doi: 10.2147/BTT.S57253. eCollection 2014.
Ref 204 Biosimilars in the therapy of inflammatory bowel diseases. Eur J Gastroenterol Hepatol. 2014 Jun;26(6):581-7. doi: 10.1097/MEG.0000000000000098.
Ref 205 Adalimumab for psoriasis patients who are non-responders to etanercept: open-label prospective evaluation. J Eur Acad Dermatol Venereol. 2009 Dec;23(12):1394-7. doi: 10.1111/j.1468-3083.2009.03325.x. Epub 2009 Jul 1.
Ref 206 TNFerade, an adenovector carrying the transgene for human tumor necrosis factor alpha, for patients with advanced solid tumors: surgical experience and long-term follow-up. Ann Surg Oncol. 2005 Oct;12(10):825-30. doi: 10.1245/ASO.2005.03.023. Epub 2005 Aug 9.
Ref 207 Case study: biosimilar anti TNFalpha (Adalimumab) analysis of Fc effector functions. BMC Proc. 2013; 7(Suppl 6): P30.
Ref 208 Emerging drugs in neuropathic pain. Expert Opin Emerg Drugs. 2007 Mar;12(1):113-26. doi: 10.1517/14728214.12.1.113.
Ref 209 RDP58, a locally active TNF inhibitor, is effective in the dextran sulphate mouse model of chronic colitis. Inflamm Res. 2002 Nov;51(11):522-31. doi: 10.1007/pl00012423.
Ref 210 Diabetes-enhanced tumor necrosis factor-alpha production promotes apoptosis and the loss of retinal microvascular cells in type 1 and type 2 models of diabetic retinopathy. Am J Pathol. 2008 May;172(5):1411-8. doi: 10.2353/ajpath.2008.071070. Epub 2008 Apr 10.
Ref 211 AP301, a synthetic peptide mimicking the lectin-like domain of TNF, enhances amiloride-sensitive Na(+) current in primary dog, pig and rat alveolar type II cells. Pulm Pharmacol Ther. 2013 Jun;26(3):356-63. doi: 10.1016/j.pupt.2012.12.011. Epub 2013 Jan 9.
Ref 212 Discovery of the inhibitors of tumor necrosis factor alpha with structure-based virtual screening. Bioorg Med Chem Lett. 2010 Nov 1;20(21):6195-8. doi: 10.1016/j.bmcl.2010.08.116. Epub 2010 Sep 16.
Ref 213 Modulation of Anti-Tumor Necrosis Factor Alpha (TNF-alpha) Antibody Secretion in Mice Immunized with TNF-alpha Kinoid. Clin Vaccine Immunol. 2012 May; 19(5): 699-703.
Ref 214 Cyclic AMP inhibition of tumor necrosis factor alpha production induced by amyloidogenic C-terminal peptide of Alzheimer's amyloid precursor protein in macrophages: involvement of multiple intracellular pathways and cyclic AMP response element binding protein. Mol Pharmacol. 2003 Mar;63(3):690-8. doi: 10.1124/mol.63.3.690.
Ref 215 DOI: 10.1136/annrheumdis-2015-eular.4042
Ref 216 Inhibition of experimental periodontitis by a topical boron-based antimicrobial. J Dent Res. 2008 Feb;87(2):148-52. doi: 10.1177/154405910808700208.
Ref 217 Pharmacokinetics and posterior segment biodistribution of ESBA105, an anti-TNF-alpha single-chain antibody, upon topical administration to the rabbit eye. Invest Ophthalmol Vis Sci. 2009 Feb;50(2):771-8. doi: 10.1167/iovs.08-2370. Epub 2008 Aug 29.
Ref 218 New developments in immunosuppressive therapy for heart transplantation. Expert Opin Emerg Drugs. 2009 Mar;14(1):1-21. doi: 10.1517/14728210902791605.
Ref 219 Clinical pipeline report, company report or official report of INmune Bio.
Ref 220 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
Ref 221 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800033173)
Ref 222 Emerging drugs for psoriasis. Expert Opin Emerg Drugs. 2009 Mar;14(1):145-63. doi: 10.1517/14728210902771334.
Ref 223 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
Ref 224 Phase I and Pharmacokinetic Studies of CYT-6091, a Novel PEGylated Colloidal Gold-rhTNF Nanomedicine. Clin Cancer Res. 2010 December 15; 16(24): 6139-6149.
Ref 225 A novel anti-rheumatic drug suppresses tumor necrosis factor-alpha and augments interleukin-10 in adjuvant arthritic rats. Eur J Pharmacol. 2000 Dec 15;409(3):331-5. doi: 10.1016/s0014-2999(00)00866-9.
Ref 226 Therapeutic Vaccination with TNF-Kinoid in TNF Antagonist-Resistant Rheumatoid Arthritis: A Phase II Randomized, Controlled Clinical Trial. PLoS One. 2014; 9(12): e113465.
Ref 227 Beta-aryl-succinic acid hydroxamates as dual inhibitors of matrix metalloproteinases and tumor necrosis factor alpha converting enzyme. J Med Chem. 2002 May 23;45(11):2289-93. doi: 10.1021/jm0110993.
Ref 228 The ChEMBL database in 2017. Nucleic Acids Res. 2017 Jan 4;45(D1):D945-D954.
Ref 229 Discovery of gamma-lactam hydroxamic acids as selective inhibitors of tumor necrosis factor alpha converting enzyme: design, synthesis, and structure-activity relationships. J Med Chem. 2002 Nov 7;45(23):4954-7. doi: 10.1021/jm0255670.
Ref 230 IND Filed for AME-527, Monoclonal Antibody That Is a Potential Treatment for Rheumatoid Arthritis. P&T Community. 2015.
Ref 231 Randomized, placebo-controlled trial of the anti-tumor necrosis factor antibody fragment afelimomab in hyperinflammatory response during severe sepsis: The RAMSES Study. Crit Care Med. 2001 Apr;29(4):765-9. doi: 10.1097/00003246-200104000-00015.
Ref 232 US patent application no. 2008,0269,123, Methods for treating polycystic kidney disease (pkd) or other cyst forming diseases.
Ref 233 AGIX-4207 [2-[4-[[1-[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]thio]-1-methylethyl]thio]-2,6-bis(1,1-dimethylethyl)phenoxy]acetic acid], a novel antioxidant and anti-inflammatory compound: cellular and biochemical characterization of antioxidant activity and inhibition of redox-sensitive inflammatory gene expression. J Pharmacol Exp Ther. 2005 May;313(2):492-501. doi: 10.1124/jpet.104.080804. Epub 2005 Feb 8.
Ref 234 CombinatoRx Drug Candidate CRx-191 Demonstrates Positive Phase 2 Results In Psoriasis. CombinatoRx. 2008.
Ref 235 US patent application no. 8007,790, Methods for treating polycystic kidney disease (pkd) or other cyst forming diseases.
Ref 236 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Target id: 2608).
Ref 237 Effect of FR133605, a novel cytokine suppressive agent, on bone and cartilage destruction in adjuvant arthritic rats. J Rheumatol. 1996 Oct;23(10):1778-83.
Ref 238 Design and development of antisense drugs. Expert Opin. Drug Discov. 2008 3(10):1189-1207.
Ref 239 CDP571, a humanized monoclonal antibody to tumour necrosis factor-alpha, for steroid-dependent Crohn's disease: a randomized, double-blind, placebo-controlled trial. Aliment Pharmacol Ther. 2006 Mar 1;23(5):617-28. doi: 10.1111/j.1365-2036.2006.02791.x.
Ref 240 Effect of the carbocyclic nucleoside analogue MDL 201,112 on inhibition of interferon-gamma-induced priming of Lewis (LEW/N) rat macrophages for enhanced respiratory burst and MHC class II Ia+ antigen expression. J Leukoc Biol. 1994 Aug;56(2):133-44. doi: 10.1002/jlb.56.2.133.