Co-Target(s) Information
Target General Information | Top | ||||
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Target ID | T59328 | Target Info | |||
Target Name | Epidermal growth factor receptor (EGFR) | ||||
Synonyms |
Receptor tyrosine-protein kinase erbB-1; Proto-oncogene c-ErbB-1; HER1; ERBB1; ERBB
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Target Type | Successful Target | ||||
Gene Name | EGFR | ||||
Biochemical Class | Kinase | ||||
UniProt ID |
Co-Targets of This Target | Top | |||||
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Co-Target Name | Vascular endothelial growth factor receptor 2 (KDR) | Successful Target | ||||
UniProt ID | VGFR2_HUMAN | |||||
Gene Name | KDR | |||||
Synonyms |
VEGFR2; VEGFR-2; VEGF-2 receptor; Protein-tyrosine kinase receptor flk-1; Kinase insert domain receptor; Fetal liver kinase 1; FLK1; FLK-1; CD309
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Representative Drug(s) | Sorafenib | Drug Info | Ki = 0.021 nM | Click to Show More | [1] | |
2 | Vandetanib | Drug Info | IC50 = 9 nM | [16] | ||
3 | VATALANIB | Drug Info | IC50 = 10 nM | [18] | ||
4 | Gefitinib | Drug Info | IC50 = 48.5 nM | [24] | ||
5 | Erlotinib | Drug Info | IC50 = 50.12 nM | [18] | ||
6 | CUDC-101 | Drug Info | IC50 = 849 nM | [10] | ||
7 | HKI-272 | Drug Info | IC50 = 858.2 nM | [38] | ||
8 | SKI-758 | Drug Info | IC50 ~ 1000 nM | [2] | ||
Co-Target Name | Tyrosine-protein kinase ABL1 (ABL) | Successful Target | ||||
UniProt ID | ABL1_HUMAN | |||||
Gene Name | ABL1 | |||||
Synonyms |
p150; Proto-oncogene tyrosine-protein kinase ABL1; Proto-oncogene c-Abl; JTK7; C-ABL; Abl; Abelson tyrosine-protein kinase 1; Abelson murine leukemia viral oncogene homolog 1
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Representative Drug(s) | SKI-758 | Drug Info | IC50 = 0.4 nM | Click to Show More | [2] | |
2 | Sorafenib | Drug Info | IC50 = 80 nM | [3] | ||
3 | Vandetanib | Drug Info | IC50 = 86 nM | [30] | ||
Co-Target Name | Proto-oncogene c-Src (SRC) | Successful Target | ||||
UniProt ID | SRC_HUMAN | |||||
Gene Name | SRC | |||||
Synonyms |
pp60c-src; Tyrosine kinase (pp60(src)); Src tyrosine kinase; SRC1; Proto-oncogene tyrosine-protein kinase Src; Pp60(src); P60-Src; C-src TK; C-Src
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Representative Drug(s) | SKI-758 | Drug Info | IC50 = 0.78 nM | Click to Show More | [2] | |
2 | Vandetanib | Drug Info | IC50 = 44 nM | [23] | ||
3 | Dacomitinib | Drug Info | IC50 = 110 nM | [29] | ||
4 | Sorafenib | Drug Info | IC50 = 390 nM | [34] | ||
Co-Target Name | Serine/threonine-protein kinase B-raf (BRAF) | Successful Target | ||||
UniProt ID | BRAF_HUMAN | |||||
Gene Name | BRAF | |||||
Synonyms |
V-Raf murine sarcoma viral oncogene homolog B1; RAFB1; Proto-oncogene B-Raf; P94; BRAF1; BRAF(V599E); BRAF serine/threonine kinase; B-raf protein; B-Raf
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Representative Drug(s) | Sorafenib | Drug Info | IC50 = 1 nM | Click to Show More | [3] | |
2 | Erlotinib | Drug Info | IC50 = 60 nM | [27] | ||
Co-Target Name | Erbb2 tyrosine kinase receptor (HER2) | Successful Target | ||||
UniProt ID | ERBB2_HUMAN | |||||
Gene Name | ERBB2 | |||||
Synonyms |
p185erbB2; Tyrosine kinase-type cell surface receptor HER2; Receptor tyrosine-protein kinase erbB-2; Proto-oncogene c-ErbB-2; Proto-oncogene Neu; NGL; NEU; Metastatic lymph node gene 19 protein; MLN19; MLN 19; HER2; CD340
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Representative Drug(s) | HKI-272 | Drug Info | IC50 = 1 nM | Click to Show More | [4] | |
2 | BIBW 2992 | Drug Info | IC50 = 2 nM | [4] | ||
3 | Varlitinib | Drug Info | IC50 = 2 nM | [6] | ||
4 | Lapatinib | Drug Info | IC50 = 2.7 nM | [7] | ||
5 | BIBX-1382 | Drug Info | IC50 = 3 nM | [8] | ||
6 | CI-1033 | Drug Info | IC50 = 5 nM | [12] | ||
7 | HM-78136B | Drug Info | IC50 = 5.3 nM | [13] | ||
8 | CUDC-101 | Drug Info | IC50 = 15.7 nM | [19] | ||
9 | BMS-599626 | Drug Info | IC50 = 22 nM | [20] | ||
10 | Gefitinib | Drug Info | IC50 = 24 nM | [21] | ||
11 | Dacomitinib | Drug Info | IC50 = 45.7 nM | [9] | ||
12 | Erlotinib | Drug Info | IC50 = 64 nM | [28] | ||
Co-Target Name | Fms-like tyrosine kinase 3 (FLT-3) | Successful Target | ||||
UniProt ID | FLT3_HUMAN | |||||
Gene Name | FLT3 | |||||
Synonyms |
Stem cell tyrosine kinase 1; STK1; STK-1; Receptor-type tyrosine-protein kinase FLT3; Fetal liver kinase-2; FLT-3; FLK2; FLK-2; FL cytokine receptor; CD135
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Representative Drug(s) | Sorafenib | Drug Info | IC50 = 1.3 nM | [5] | ||
Co-Target Name | Erbb4 tyrosine kinase receptor (Erbb-4) | Successful Target | ||||
UniProt ID | ERBB4_HUMAN | |||||
Gene Name | ERBB4 | |||||
Synonyms |
Tyrosine kinase-type cell surface receptor HER4; Receptor tyrosine-protein kinase erbB-4; Proto-oncogene-like protein c-ErbB-4; P180erbB4; HER4
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Representative Drug(s) | Varlitinib | Drug Info | IC50 = 4 nM | Click to Show More | [9] | |
2 | CI-1033 | Drug Info | IC50 = 10 nM | [12] | ||
3 | Dacomitinib | Drug Info | IC50 = 74 nM | [29] | ||
4 | BMS-599626 | Drug Info | IC50 = 190 nM | [20] | ||
5 | Gefitinib | Drug Info | IC50 = 476 nM | [29] | ||
6 | Lapatinib | Drug Info | IC50 ~ 1000 nM | [40] | ||
Co-Target Name | Histone deacetylase (HDAC) | Successful Target | ||||
UniProt ID | HDAC1_HUMAN; HDAC2_HUMAN; HDAC3_HUMAN; HDAC4_HUMAN; HDAC5_HUMAN; HDAC6_HUMAN; HDAC7_HUMAN; HDAC8_HUMAN; HDAC9_HUMAN; HDA10_HUMAN; HDA11_HUMAN | |||||
Gene Name | NO-GeName | |||||
Synonyms |
Human histone deacetylase
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Representative Drug(s) | CUDC-101 | Drug Info | IC50 = 4.4 nM | [10] | ||
Co-Target Name | Histone deacetylase 1 (HDAC1) | Successful Target | ||||
UniProt ID | HDAC1_HUMAN | |||||
Gene Name | HDAC1 | |||||
Synonyms |
RPD3L1; HD1
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Representative Drug(s) | CUDC-101 | Drug Info | IC50 = 4.5 nM | [10] | ||
Co-Target Name | Fibroblast growth factor receptor 1 (FGFR1) | Successful Target | ||||
UniProt ID | FGFR1_HUMAN | |||||
Gene Name | FGFR1 | |||||
Synonyms |
c-fgr; bFGF-R-1; bFGF-R; N-sam; HBGFR; Fms-like tyrosine kinase 2; FLT2; FLT-2; FLG; FGFR-1; FGFBR; CEK; CD331 antigen; CD331; Basic fibroblast growth factor receptor 1; BFGFR
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Representative Drug(s) | Sorafenib | Drug Info | IC50 = 4.63 nM | [11] | ||
Co-Target Name | Proto-oncogene c-Ret (RET) | Successful Target | ||||
UniProt ID | RET_HUMAN | |||||
Gene Name | RET | |||||
Synonyms |
RET51; RET receptor tyrosine kinase; RET mutant Y791F; RET mutant V804M; RET mutant V804L; RET mutant S891A; RET mutant M918T; RET mutant G691S; Proto-oncogene tyrosine-protein kinase receptor Ret; PTC; Cadherin family member 12; CDHR16; CDHF12; C-ret
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Representative Drug(s) | Sorafenib | Drug Info | IC50 = 6 nM | Click to Show More | [14] | |
2 | Vandetanib | Drug Info | IC50 = 49 nM | [25] | ||
Co-Target Name | Inosine-5'-monophosphate dehydrogenase (IMPDH) | Successful Target | ||||
UniProt ID | IMDH1_HUMAN; IMDH2_HUMAN | |||||
Gene Name | NO-GeName | |||||
Representative Drug(s) | Merimepodib | Drug Info | IC50 = 7 nM | [15] | ||
Co-Target Name | Inosine-5'-monophosphate dehydrogenase 2 (IMPDH2) | Successful Target | ||||
UniProt ID | IMDH2_HUMAN | |||||
Gene Name | IMPDH2 | |||||
Synonyms |
IMPDH-II; IMPDH 2; IMPD2; IMPD 2; IMP dehydrogenase 2
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Representative Drug(s) | Merimepodib | Drug Info | IC50 = 10 nM | [17] | ||
Co-Target Name | Tyrosine-protein kinase Kit (KIT) | Successful Target | ||||
UniProt ID | KIT_HUMAN | |||||
Gene Name | KIT | |||||
Synonyms |
v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog; p145 c-kit; Proto-oncogene tyrosine-protein kinase Kit; Proto-oncogene c-Kit; Piebald trait protein; PBT; Mast/stem cell growth factor receptor Kit; CD117 antigen; CD117; C-kit
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Representative Drug(s) | Sorafenib | Drug Info | IC50 = 10 nM | Click to Show More | [3] | |
2 | Vandetanib | Drug Info | IC50 = 343 nM | [30] | ||
3 | VATALANIB | Drug Info | IC50 = 730 nM | [37] | ||
Co-Target Name | Platelet-derived growth factor receptor beta (PDGFRB) | Successful Target | ||||
UniProt ID | PGFRB_HUMAN | |||||
Gene Name | PDGFRB | |||||
Synonyms |
Platelet-derived growth factor receptor 1; PDGFR1; PDGFR-beta; PDGFR-1; PDGFR; PDGF-R-beta; CD140b antigen; CD140b; CD140 antigen-like family member B; Beta-type platelet-derived growth factor receptor; Beta-PDGFR; Beta platelet-derived growth factor receptor
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Representative Drug(s) | Sorafenib | Drug Info | IC50 = 10 nM | Click to Show More | [3] | |
2 | Vandetanib | Drug Info | IC50 = 477 nM | [30] | ||
3 | VATALANIB | Drug Info | IC50 = 490 nM | [35] | ||
Co-Target Name | LCK tyrosine protein kinase (LCK) | Successful Target | ||||
UniProt ID | LCK_HUMAN | |||||
Gene Name | LCK | |||||
Synonyms |
p56-LCK; Tyrosine-protein kinase Lck; T cell-specific protein-tyrosine kinase; Proto-oncogene tyrosine-protein kinase LCK; Proto-oncogene Lck; Protein YT16; Lymphocyte cell-specific protein-tyrosine kinase; Leukocyte C-terminal Src kinase; LSK; LCK p59-Fyn; LCK Protooncogene Syn
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Representative Drug(s) | SKI-758 | Drug Info | IC50 = 20 nM | Click to Show More | [2] | |
2 | Sorafenib | Drug Info | IC50 = 60 nM | [3] | ||
3 | Dacomitinib | Drug Info | IC50 = 94 nM | [29] | ||
Co-Target Name | Vascular endothelial growth factor receptor (VEGFR) | Successful Target | ||||
UniProt ID | VGFR1_HUMAN; VGFR2_HUMAN; VGFR3_HUMAN | |||||
Gene Name | NO-GeName | |||||
Representative Drug(s) | Vandetanib | Drug Info | IC50 = 25 nM | Click to Show More | [22] | |
2 | VATALANIB | Drug Info | IC50 = 100 nM | [16] | ||
3 | Erlotinib | Drug Info | IC50 = 250 nM | [33] | ||
Co-Target Name | 5-HT 2B receptor (HTR2B) | Successful Target | ||||
UniProt ID | 5HT2B_HUMAN | |||||
Gene Name | HTR2B | |||||
Synonyms |
Serotonin receptor 2B; 5-hydroxytryptamine receptor 2B; 5-HT2B; 5-HT-2B; 5-HT 2B
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Representative Drug(s) | Sorafenib | Drug Info | Ki = 56 nM | [26] | ||
Co-Target Name | ALK tyrosine kinase receptor (ALK) | Successful Target | ||||
UniProt ID | ALK_HUMAN | |||||
Gene Name | ALK | |||||
Synonyms |
CD246; Anaplastic lymphoma kinase
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Representative Drug(s) | Osimertinib | Drug Info | IC50 = 177 nM | [31] | ||
Co-Target Name | Tyrosine-protein kinase BTK (ATK) | Successful Target | ||||
UniProt ID | BTK_HUMAN | |||||
Gene Name | BTK | |||||
Synonyms |
Bruton's tyrosine kinase; Bruton tyrosine kinase; BPK; B-cell progenitor kinase; B cell progenitor kinase; Agammaglobulinemia tyrosine kinase; Agammaglobulinaemia tyrosine kinase; AGMX1
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Representative Drug(s) | CI-1033 | Drug Info | IC50 = 185 nM | [32] | ||
Co-Target Name | 5-HT 2C receptor (HTR2C) | Successful Target | ||||
UniProt ID | 5HT2C_HUMAN | |||||
Gene Name | HTR2C | |||||
Synonyms |
Serotonin receptor 2C; HTR1C; 5HT-1C; 5-hydroxytryptamine receptor 2C; 5-hydroxytryptamine receptor 1C; 5-HTR2C; 5-HT2C receptor; 5-HT2C; 5-HT1C; 5-HT-2C; 5-HT-1C
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Representative Drug(s) | Sorafenib | Drug Info | Ki = 417 nM | [26] | ||
Co-Target Name | Voltage-gated potassium channel Kv11.1 (KCNH2) | Successful Target | ||||
UniProt ID | KCNH2_HUMAN | |||||
Gene Name | KCNH2 | |||||
Synonyms |
hERG1; hERG-1; Voltage-gated potassium channel subunit Kv11.1; Potassium voltage-gated channel subfamily H member 2; HERG K+ channel; HERG; H-ERG; Ether-a-go-go-related protein 1; Ether-a-go-go-related gene potassium channel 1; Ether-a-go-go related protein 1; Ether-a-go-go related gene potassium channel 1; Eag related protein 1; Eag homolog; ERG-1; ERG
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Representative Drug(s) | Osimertinib | Drug Info | IC50 = 570 nM | Click to Show More | [36] | |
2 | Lapatinib | Drug Info | IC50 = 1000 nM | [41] | ||
Co-Target Name | Insulin receptor (INSR) | Successful Target | ||||
UniProt ID | INSR_HUMAN | |||||
Gene Name | INSR | |||||
Synonyms |
IR; CD220 antigen; CD220
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Representative Drug(s) | Osimertinib | Drug Info | IC50 = 912 nM | [39] | ||
Co-Target Name | Cyclin-dependent kinase 4 (CDK4) | Successful Target | ||||
UniProt ID | CDK4_HUMAN | |||||
Gene Name | CDK4 | |||||
Synonyms |
PSK-J3; Cell division protein kinase 4
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Representative Drug(s) | SKI-758 | Drug Info | IC50 ~ 1000 nM | [2] | ||
Co-Target Name | Janus kinase 3 (JAK-3) | Successful Target | ||||
UniProt ID | JAK3_HUMAN | |||||
Gene Name | JAK3 | |||||
Synonyms |
Tyrosine-protein kinase JAK3; Leukocyte janus kinase; L-JAK
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Representative Drug(s) | Gefitinib | Drug Info | IC50 ~ 1000 nM | [29] | ||
Co-Target Name | Ephrin type-B receptor 4 (EPHB4) | Clinical trial Target | ||||
UniProt ID | EPHB4_HUMAN | |||||
Gene Name | EPHB4 | |||||
Synonyms |
Tyrosine-protein kinase TYRO11; TYRO11; MYK1; Hepatoma transmembrane kinase; HTK
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Representative Drug(s) | Sorafenib | Drug Info | IC50 = 0.2 nM | Click to Show More | [42] | |
2 | Gefitinib | Drug Info | IC50 = 1000 nM | [34] | ||
Co-Target Name | Angiopoietin 1 receptor (TEK) | Clinical trial Target | ||||
UniProt ID | TIE2_HUMAN | |||||
Gene Name | TEK | |||||
Synonyms |
hTIE2; VMCM1; VMCM; Tyrosine-protein kinase receptor TIE-2; Tyrosine-protein kinase receptor TEK; Tyrosine kinase with Ig and EGF homology domains-2; Tunica interna endothelial cell kinase; TIE2; P140 TEK; Endothelial tyrosine kinase; Endothelial Cell-Specific Receptor TIE-2; CD202b antigen; CD202b
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Representative Drug(s) | Sorafenib | Drug Info | IC50 = 0.39 nM | Click to Show More | [43] | |
2 | Vandetanib | Drug Info | IC50 = 567 nM | [30] | ||
Co-Target Name | Proto-oncogene c-RAF (c-RAF) | Clinical trial Target | ||||
UniProt ID | RAF1_HUMAN | |||||
Gene Name | RAF1 | |||||
Synonyms |
cRaf; Raf-1; RAF proto-oncogene serine/threonine-protein kinase; RAF
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Representative Drug(s) | Sorafenib | Drug Info | IC50 = 1 nM | [3] | ||
Co-Target Name | Erbb3 tyrosine kinase receptor (Erbb-3) | Clinical trial Target | ||||
UniProt ID | ERBB3_HUMAN | |||||
Gene Name | ERBB3 | |||||
Synonyms |
Tyrosine kinase-type cell surface receptor HER3; Receptor tyrosine-protein kinase erbB-3; Proto-oncogene-like protein c-ErbB-3; HER3; C-erbB3; C-erbB-3 protein
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Representative Drug(s) | Osimertinib | Drug Info | IC50 = 2.1 nM | Click to Show More | [44] | |
2 | Erlotinib | Drug Info | IC50 = 10 nM | [46] | ||
3 | CO-1686 | Drug Info | IC50 = 46 nM | [46] | ||
Co-Target Name | Vascular endothelial growth factor receptor 3 (FLT-4) | Clinical trial Target | ||||
UniProt ID | VGFR3_HUMAN | |||||
Gene Name | FLT4 | |||||
Synonyms |
VEGFR3; VEGFR-3; VEGF-3 receptor; Tyrosine-protein kinase receptor FLT4; Fms-like tyrosine kinase 4
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Representative Drug(s) | Sorafenib | Drug Info | IC50 = 3 nM | Click to Show More | [45] | |
2 | VATALANIB | Drug Info | IC50 = 195 nM | [51] | ||
3 | Vandetanib | Drug Info | IC50 = 233 nM | [30] | ||
Co-Target Name | Histone deacetylase 6 (HDAC6) | Clinical trial Target | ||||
UniProt ID | HDAC6_HUMAN | |||||
Gene Name | HDAC6 | |||||
Synonyms |
KIAA0901; JM21; HD6
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Representative Drug(s) | CUDC-101 | Drug Info | IC50 = 5.1 nM | [10] | ||
Co-Target Name | Histone deacetylase 3 (HDAC3) | Clinical trial Target | ||||
UniProt ID | HDAC3_HUMAN | |||||
Gene Name | HDAC3 | |||||
Synonyms |
SMAP45; RPD32; RPD3-2; HD3
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Representative Drug(s) | CUDC-101 | Drug Info | IC50 = 9.1 nM | [10] | ||
Co-Target Name | Soluble epoxide hydrolase (EPHX2) | Clinical trial Target | ||||
UniProt ID | HYES_HUMAN | |||||
Gene Name | EPHX2 | |||||
Synonyms |
Bifunctional epoxide hydrolase 2
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Representative Drug(s) | Sorafenib | Drug Info | IC50 = 12 nM | [47] | ||
Co-Target Name | Histone deacetylase 2 (HDAC2) | Clinical trial Target | ||||
UniProt ID | HDAC2_HUMAN | |||||
Gene Name | HDAC2 | |||||
Synonyms |
HD2
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Representative Drug(s) | CUDC-101 | Drug Info | IC50 = 12.6 nM | [10] | ||
Co-Target Name | Histone deacetylase 4 (HDAC4) | Clinical trial Target | ||||
UniProt ID | HDAC4_HUMAN | |||||
Gene Name | HDAC4 | |||||
Synonyms |
KIAA0288; HD4
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Representative Drug(s) | CUDC-101 | Drug Info | IC50 = 13.2 nM | [10] | ||
Co-Target Name | Vascular endothelial growth factor receptor 1 (FLT-1) | Clinical trial Target | ||||
UniProt ID | VGFR1_HUMAN | |||||
Gene Name | FLT1 | |||||
Synonyms |
Vascular permeability factor receptor; VEGFR1; VEGFR-1; VEGF-1 receptor; Tyrosine-protein kinase receptor FLT; Tyrosine-protein kinase FRT; Fms-like tyrosine kinase 1; FRT; FLT
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Representative Drug(s) | Sorafenib | Drug Info | IC50 = 18 nM | Click to Show More | [48] | |
2 | Vandetanib | Drug Info | IC50 = 22 nM | [50] | ||
3 | VATALANIB | Drug Info | IC50 = 54 nM | [50] | ||
4 | Erlotinib | Drug Info | IC50 ~ 1000 nM | [54] | ||
Co-Target Name | Extracellular signal-regulated kinase 1 (ERK1) | Clinical trial Target | ||||
UniProt ID | MK03_HUMAN | |||||
Gene Name | MAPK3 | |||||
Synonyms |
PRKM3; P44-MAPK; P44-ERK1; P44 Mitogen-activated protein kinase; Mitogen-activated protein kinase 3; Microtubule-associated protein-2 kinase; Microtubule-associated protein 2 kinase; MAPK 3; MAP kinase isoform p44; MAP kinase 3; Insulin-stimulated MAP2 kinase; ERT2; ERK-1
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Representative Drug(s) | Sorafenib | Drug Info | IC50 = 18.1 nM | [49] | ||
Co-Target Name | Macrophage colony-stimulating factor 1 receptor (CSF1R) | Clinical trial Target | ||||
UniProt ID | CSF1R_HUMAN | |||||
Gene Name | CSF1R | |||||
Synonyms |
Proto-oncogene c-Fms; M-CSF-R; FMS; CSF-1R; CSF-1-R; CSF-1 receptor; CD115
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Representative Drug(s) | Sorafenib | Drug Info | IC50 = 19 nM | [3] | ||
Co-Target Name | Stress-activated protein kinase 2a (p38 alpha) | Clinical trial Target | ||||
UniProt ID | MK14_HUMAN | |||||
Gene Name | MAPK14 | |||||
Synonyms |
SAPK2A; P38 mitogen activatedprotein kinase; P38 Mitogen-activatedprotein kinase alpha; Mitogen-activated protein kinase p38 alpha; Mitogen-activated protein kinase 14; MXI2; MAX-interacting protein 2; MAPK 14; MAP kinase p38alpha; MAP kinase p38 alpha; MAP kinase MXI2; MAP kinase 14; Cytokine suppressive anti-inflammatory drug-binding protein; Cytokine suppressive anti-inflammatory drug binding protein; CSPB1; CSBP2; CSBP1; CSBP; CSAID-binding protein; CSAID binding protein; CRK1
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Representative Drug(s) | Sorafenib | Drug Info | IC50 = 37.4 nM | [49] | ||
Co-Target Name | Extracellular signal-regulated kinase 2 (ERK2) | Clinical trial Target | ||||
UniProt ID | MK01_HUMAN | |||||
Gene Name | MAPK1 | |||||
Synonyms |
PRKM2; PRKM1; P42-MAPK; P42 Mitogen-activated protein kinase; Mitogen-activated protein kinase 2; Mitogen-activated protein kinase 1; MAPK 2; MAPK 1; MAP kinase isoform p42; MAP kinase 2; MAP kinase 1; ERT1; ERK-2
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Representative Drug(s) | Sorafenib | Drug Info | IC50 = 109.5 nM | [49] | ||
Co-Target Name | MAP kinase signal-integrating kinase 2 (MKNK2) | Clinical trial Target | ||||
UniProt ID | MKNK2_HUMAN | |||||
Gene Name | MKNK2 | |||||
Synonyms |
Mnk2; MAPK signal-integrating kinase 2
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Representative Drug(s) | Sorafenib | Drug Info | IC50 = 262 nM | [52] | ||
Co-Target Name | HUMAN cyclin G-associated kinase (GAK) | Clinical trial Target | ||||
UniProt ID | GAK_HUMAN | |||||
Gene Name | GAK | |||||
Synonyms |
cyclin G associated kinase
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Representative Drug(s) | Gefitinib | Drug Info | IC50 = 420 nM | Click to Show More | [53] | |
2 | Erlotinib | Drug Info | IC50 = 910 nM | [53] | ||
Co-Target Name | Tyrosine-protein kinase Lyn (JTK8) | Clinical trial Target | ||||
UniProt ID | LYN_HUMAN | |||||
Gene Name | LYN | |||||
Synonyms |
p56Lyn; p53Lyn; V-yes-1 Yamaguchi sarcoma viral related oncogene homolog; Lck/Yes-related novel protein tyrosine kinase
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Representative Drug(s) | CUDC-101 | Drug Info | IC50 = 840 nM | [10] | ||
Co-Target Name | RAC-alpha serine/threonine-protein kinase (AKT1) | Clinical trial Target | ||||
UniProt ID | AKT1_HUMAN | |||||
Gene Name | AKT1 | |||||
Synonyms |
RAC-PK-alpha; RAC; Proto-oncogene c-Akt; Protein kinase B alpha; PKB alpha
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Representative Drug(s) | SKI-758 | Drug Info | IC50 ~ 1000 nM | [2] | ||
Co-Target Name | Phosphoinositide dependent protein kinase-1 (PDPK1) | Clinical trial Target | ||||
UniProt ID | PDPK1_HUMAN | |||||
Gene Name | PDPK1 | |||||
Synonyms |
PDK1; HPDK1; 3-phosphoinositide-dependent protein kinase 1; 3-Phosphoinositide-dependent kinase-1; 3'-phosphoinositide dependent kinase 1
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Representative Drug(s) | SKI-758 | Drug Info | IC50 ~ 1000 nM | [2] | ||
Co-Target Name | Discoidin domain-containing receptor 2 (DDR2) | Patented-recorded Target | ||||
UniProt ID | DDR2_HUMAN | |||||
Gene Name | DDR2 | |||||
Synonyms |
Tyrosine-protein kinase TYRO10; Receptor protein-tyrosine kinase TKT; Neurotrophic tyrosine kinase, receptor-related 3; Discoidin domain-containing receptor tyrosine kinase 2; Discoidin domain receptor 2; DDR2; CD167 antigen-like family member B
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Representative Drug(s) | Sorafenib | Drug Info | IC50 = 7 nM | [55] | ||
Co-Target Name | Histone deacetylase 5 (HDAC5) | Patented-recorded Target | ||||
UniProt ID | HDAC5_HUMAN | |||||
Gene Name | HDAC5 | |||||
Synonyms |
KIAA0600; HD5; Antigen NY-CO-9
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Representative Drug(s) | CUDC-101 | Drug Info | IC50 = 11.4 nM | [10] | ||
Co-Target Name | Histone deacetylase 10 (HDAC10) | Patented-recorded Target | ||||
UniProt ID | HDA10_HUMAN | |||||
Gene Name | HDAC10 | |||||
Synonyms |
Polyamine deacetylase HDAC10; HD10
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Representative Drug(s) | CUDC-101 | Drug Info | IC50 = 26.1 nM | [10] | ||
Co-Target Name | B lymphocyte kinase (BLK) | Patented-recorded Target | ||||
UniProt ID | BLK_HUMAN | |||||
Gene Name | BLK | |||||
Synonyms |
p55-Blk; Tyrosine-protein kinase Blk
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Representative Drug(s) | CI-1033 | Drug Info | IC50 = 29 nM | [32] | ||
Co-Target Name | Tyrosine-protein kinase BMX (BMX) | Patented-recorded Target | ||||
UniProt ID | BMX_HUMAN | |||||
Gene Name | BMX | |||||
Synonyms |
NTK38; Epithelial and endothelial tyrosine kinase; ETK; Cytoplasmic tyrosine-protein kinase BMX; Bone marrow tyrosine kinase gene in chromosome X protein
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Representative Drug(s) | CI-1033 | Drug Info | IC50 = 62 nM | [32] | ||
Co-Target Name | Histone deacetylase 9 (HDAC9) | Patented-recorded Target | ||||
UniProt ID | HDAC9_HUMAN | |||||
Gene Name | HDAC9 | |||||
Synonyms |
MITR; MEF2-interacting transcription repressor MITR; KIAA0744; Histone deacetylase-related protein; Histone deacetylase 7B; HDRP; HDAC7B; HDAC7; HD9; HD7b
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Representative Drug(s) | CUDC-101 | Drug Info | IC50 = 67.2 nM | [10] | ||
Co-Target Name | Histone deacetylase 8 (HDAC8) | Patented-recorded Target | ||||
UniProt ID | HDAC8_HUMAN | |||||
Gene Name | HDAC8 | |||||
Synonyms |
Histone deacetylase-8; HDACL1; HD8; CDA07
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Representative Drug(s) | CUDC-101 | Drug Info | IC50 = 79.8 nM | [10] | ||
Co-Target Name | Hematopoietic cell kinase (HCK) | Patented-recorded Target | ||||
UniProt ID | HCK_HUMAN | |||||
Gene Name | HCK | |||||
Synonyms |
p61Hck; p59Hck; p59-HCK/p60-HCK; Tyrosine-protein kinase HCK; Hemopoietic cell kinase
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Representative Drug(s) | Gefitinib | Drug Info | IC50 = 110 nM | Click to Show More | [34] | |
2 | Sorafenib | Drug Info | IC50 = 530 nM | [34] | ||
Co-Target Name | Cyclin-dependent kinase 8 (CDK8) | Patented-recorded Target | ||||
UniProt ID | CDK8_HUMAN | |||||
Gene Name | CDK8 | |||||
Synonyms |
Protein kinase K35; Mediator of RNA polymerase II transcription subunit CDK8; Mediator complex subunit CDK8; Cell division protein kinase 8
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Representative Drug(s) | Sorafenib | Drug Info | IC50 = 199 nM | [56] | ||
Co-Target Name | Casein kinase I alpha (CSNK1A1) | Patented-recorded Target | ||||
UniProt ID | KC1A_HUMAN | |||||
Gene Name | CSNK1A1 | |||||
Synonyms |
Casein kinase I isoform alpha; CKI-alpha; CK1
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Representative Drug(s) | Sorafenib | Drug Info | IC50 = 250 nM | [34] | ||
Co-Target Name | Histone deacetylase 7 (HDAC7) | Patented-recorded Target | ||||
UniProt ID | HDAC7_HUMAN | |||||
Gene Name | HDAC7 | |||||
Synonyms |
Histone deacetylase 7A; HDAC7A; HD7a; HD7
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Representative Drug(s) | CUDC-101 | Drug Info | IC50 = 373 nM | [10] | ||
Co-Target Name | NIMA-related kinase 2 (NEK2) | Literature-reported Target | ||||
UniProt ID | NEK2_HUMAN | |||||
Gene Name | NEK2 | |||||
Synonyms |
Serine/threonine-protein kinase Nek2; NimA-related protein kinase 2; NimA-like protein kinase 1; Never in mitosis A-related kinase 2; NLK1; NEK2A; HSPK 21
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Representative Drug(s) | HKI-272 | Drug Info | IC50 = 274 nM | Click to Show More | [57] | |
2 | Pelitinib | Drug Info | IC50 = 661 nM | [57] | ||
Co-Target Name | Organic anion transporter B (SLCO2B1) | Literature-reported Target | ||||
UniProt ID | SO2B1_HUMAN | |||||
Gene Name | SLCO2B1 | |||||
Synonyms |
Solute carrier organic anion transporter family member 2B1; Solute carrier family 21 member 9; SLC21A9; Organic anion transporter polypeptide-related protein 2; OATPRP2; OATPB; OATP2B1; OATP-RP2; OATP-B; KIAA0880
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Representative Drug(s) | Erlotinib | Drug Info | Ki = 530 nM | [58] | ||
Co-Target Name | Serine/threonine-protein kinase A-Raf (ARAF) | Co-Target | ||||
UniProt ID | ARAF_HUMAN | |||||
Gene Name | ARAF | |||||
Synonyms |
Proto-oncogene A-Raf; Proto-oncogene A-Raf-1; Proto-oncogene Pks
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Representative Drug(s) | Sorafenib | Drug Info | IC50 = 7.1 nM | [59] | ||
Co-Target Name | Cyclin dependent kinase 8-Cyclin C complex (CDK8-CCNC) | Co-Target | ||||
UniProt ID | CDK8_HUMAN-CCNC_HUMAN | |||||
Gene Name | CDK8-CCNC | |||||
Representative Drug(s) | Sorafenib | Drug Info | IC50 = 32.5 nM | [60] | ||
Co-Target Name | Cyclin-dependent kinase 19 (CDK19) | Co-Target | ||||
UniProt ID | CDK19_HUMAN | |||||
Gene Name | CDK19 | |||||
Synonyms |
CDC2-related protein kinase 6; Cell division cycle 2-like protein kinase 6; Cell division protein kinase 19; Cyclin-dependent kinase 11; Death-preventing kinase
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Representative Drug(s) | Sorafenib | Drug Info | IC50 = 206 nM | [56] | ||
Co-Target Name | Kinesin 1 heavy chain-Tyrosine protein kinase receptor RET (KIF5B-RET) | Co-Target | ||||
UniProt ID | KINH_HUMAN-RET_HUMAN | |||||
Gene Name | KIF5B-RET | |||||
Representative Drug(s) | Vandetanib | Drug Info | IC50 = 400 nM | [25] |
References | Top | ||||
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