Found 31 hits with Last Name = 'abd el-karim' and Initial = 'ss' Target/Host
(Institution) | Ligand | Target/Host
Links | Ligand
Links | Trg + Lig
Links | Ki
nM | ΔG°
kJ/mole | IC50
nM | Kd
nM | EC50/IC50
nM | koff
s-1 | kon
M-1s-1 | pH | Temp
°C |
|---|
Serine/threonine-protein kinase B-raf
(Homo sapiens (Human)) | BDBM50428286
(DABRAFENIB | GSK2118436A)Show SMILES CC(C)(C)c1nc(c(s1)-c1ccnc(N)n1)-c1cccc(NS(=O)(=O)c2c(F)cccc2F)c1F Show InChI InChI=1S/C23H20F3N5O2S2/c1-23(2,3)21-30-18(19(34-21)16-10-11-28-22(27)29-16)12-6-4-9-15(17(12)26)31-35(32,33)20-13(24)7-5-8-14(20)25/h4-11,31H,1-3H3,(H2,27,28,29) | PDB
MMDB
NCI pathway
Reactome pathway
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| DrugBank
PDB
Article
PubMed
| n/a | n/a | 0.700 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of BRAF V600E mutant (unknown origin) |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair | 
3D Structure (crystal) |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM13216
(BMS-354825 | CHEMBL1421 | DASATINIB | N-(2-Chloro-...)Show SMILES Cc1nc(Nc2ncc(s2)C(=O)Nc2c(C)cccc2Cl)cc(n1)N1CCN(CCO)CC1 Show InChI InChI=1S/C22H26ClN7O2S/c1-14-4-3-5-16(23)20(14)28-21(32)17-13-24-22(33-17)27-18-12-19(26-15(2)25-18)30-8-6-29(7-9-30)10-11-31/h3-5,12-13,31H,6-11H2,1-2H3,(H,28,32)(H,24,25,26,27) | PDB
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| Article
PubMed
| n/a | n/a | 1 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of c-kit (unknown origin) |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM13216
(BMS-354825 | CHEMBL1421 | DASATINIB | N-(2-Chloro-...)Show SMILES Cc1nc(Nc2ncc(s2)C(=O)Nc2c(C)cccc2Cl)cc(n1)N1CCN(CCO)CC1 Show InChI InChI=1S/C22H26ClN7O2S/c1-14-4-3-5-16(23)20(14)28-21(32)17-13-24-22(33-17)27-18-12-19(26-15(2)25-18)30-8-6-29(7-9-30)10-11-31/h3-5,12-13,31H,6-11H2,1-2H3,(H,28,32)(H,24,25,26,27) | PDB
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| DrugBank
Article
PubMed
| n/a | n/a | 1 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of Src (unknown origin) |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase ABL1
(Homo sapiens (Human)) | BDBM13216
(BMS-354825 | CHEMBL1421 | DASATINIB | N-(2-Chloro-...)Show SMILES Cc1nc(Nc2ncc(s2)C(=O)Nc2c(C)cccc2Cl)cc(n1)N1CCN(CCO)CC1 Show InChI InChI=1S/C22H26ClN7O2S/c1-14-4-3-5-16(23)20(14)28-21(32)17-13-24-22(33-17)27-18-12-19(26-15(2)25-18)30-8-6-29(7-9-30)10-11-31/h3-5,12-13,31H,6-11H2,1-2H3,(H,28,32)(H,24,25,26,27) | PDB
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| DrugBank
PDB
Article
PubMed
| n/a | n/a | 1 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of ABL (unknown origin) |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM5446
(CHEMBL553 | ERLOTINIB HYDROCHLORIDE | Erlotinib | ...)Show InChI InChI=1S/C22H23N3O4/c1-4-16-6-5-7-17(12-16)25-22-18-13-20(28-10-8-26-2)21(29-11-9-27-3)14-19(18)23-15-24-22/h1,5-7,12-15H,8-11H2,2-3H3,(H,23,24,25) | PDB
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| DrugBank
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Article
PubMed
| n/a | n/a | 2 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM112499
(DACOMITINIB | US8623883, No. 2 | WO2022090481, Exa...)Show SMILES COc1cc2ncnc(Nc3ccc(F)c(Cl)c3)c2cc1NC(=O)\C=C\CN1CCCCC1 Show InChI InChI=1S/C24H25ClFN5O2/c1-33-22-14-20-17(24(28-15-27-20)29-16-7-8-19(26)18(25)12-16)13-21(22)30-23(32)6-5-11-31-9-3-2-4-10-31/h5-8,12-15H,2-4,9-11H2,1H3,(H,30,32)(H,27,28,29)/b6-5+ | PDB
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| PDB
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| n/a | n/a | 6 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50322823
((S)-N-(4-(3-chloro-4-fluorophenylamino)-7-(tetrahy...)Show SMILES CN(C)C\C=C\C(=O)Nc1cc2c(Nc3ccc(F)c(Cl)c3)ncnc2cc1O[C@H]1CCOC1 |r| Show InChI InChI=1S/C24H25ClFN5O3/c1-31(2)8-3-4-23(32)30-21-11-17-20(12-22(21)34-16-7-9-33-13-16)27-14-28-24(17)29-15-5-6-19(26)18(25)10-15/h3-6,10-12,14,16H,7-9,13H2,1-2H3,(H,30,32)(H,27,28,29)/b4-3+/t16-/m0/s1 | PDB
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| n/a | n/a | 10 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM5445
(CHEMBL554 | GW572016 | LAPATINIB DITOSYLATE | Lapa...)Show SMILES CS(=O)(=O)CCNCc1ccc(o1)-c1ccc2ncnc(Nc3ccc(OCc4cccc(F)c4)c(Cl)c3)c2c1 Show InChI InChI=1S/C29H26ClFN4O4S/c1-40(36,37)12-11-32-16-23-7-10-27(39-23)20-5-8-26-24(14-20)29(34-18-33-26)35-22-6-9-28(25(30)15-22)38-17-19-3-2-4-21(31)13-19/h2-10,13-15,18,32H,11-12,16-17H2,1H3,(H,33,34,35) | PDB
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| n/a | n/a | 11 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50029668
(AZD-9291 | Osimertinib | US10085983, Compound AZD-...)Show SMILES COc1cc(N(C)CCN(C)C)c(NC(=O)C=C)cc1Nc1nccc(n1)-c1cn(C)c2ccccc12 Show InChI InChI=1S/C28H33N7O2/c1-7-27(36)30-22-16-23(26(37-6)17-25(22)34(4)15-14-33(2)3)32-28-29-13-12-21(31-28)20-18-35(5)24-11-9-8-10-19(20)24/h7-13,16-18H,1,14-15H2,2-6H3,(H,30,36)(H,29,31,32) | PDB
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| DrugBank
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| n/a | n/a | 13 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Dual specificity mitogen-activated protein kinase kinase 1/2
(Homo sapiens (Human)) | BDBM50355497
(AZD-6244 | CHEMBL1614701)Show SMILES Cn1cnc2c(F)c(Nc3ccc(Br)cc3Cl)c(cc12)C(=O)NOCCO Show InChI InChI=1S/C17H15BrClFN4O3/c1-24-8-21-16-13(24)7-10(17(26)23-27-5-4-25)15(14(16)20)22-12-3-2-9(18)6-11(12)19/h2-3,6-8,22,25H,4-5H2,1H3,(H,23,26) | PDB
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| n/a | n/a | 14 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of MEK (unknown origin) |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM5447
(CHEMBL939 | GEFITINIB | Iressa | N-(3-Chloro-4-flu...)Show SMILES COc1cc2ncnc(Nc3ccc(F)c(Cl)c3)c2cc1OCCCN1CCOCC1 Show InChI InChI=1S/C22H24ClFN4O3/c1-29-20-13-19-16(12-21(20)31-8-2-5-28-6-9-30-10-7-28)22(26-14-25-19)27-15-3-4-18(24)17(23)11-15/h3-4,11-14H,2,5-10H2,1H3,(H,25,26,27) | PDB
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| DrugBank
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PDB
Article
PubMed
| n/a | n/a | 37 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50561030
(CHEMBL4750734)Show SMILES Cn1c(nc2ccccc12)-c1csc(N\N=C/c2ccc(o2)[N+]([O-])=O)n1 | PDB
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| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 72 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) using ATF-2 as substrate after 1 hr by radiometric based ELISA |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50561024
(CHEMBL4753631)Show SMILES Cn1c(nc2ccccc12)-c1csc(N\N=C/c2ccc(cc2)[N+]([O-])=O)n1 | PDB
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| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 85 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) using ATF-2 as substrate after 1 hr by radiometric based ELISA |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50561025
(CHEMBL4786168)Show SMILES CN(C)c1ccc(\C=N/Nc2nc(cs2)-c2nc3ccccc3n2C)cc1 | PDB
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| PC cid
PC sid
UniChem
| Article
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| n/a | n/a | 104 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) using ATF-2 as substrate after 1 hr by radiometric based ELISA |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50561017
(CHEMBL4780058)Show SMILES [#6]-n1c(nc2ccccc12)-c1csc(-[#7]\[#7]=[#6]-2\[#6]-[#6]-[#6]-[#6]-2)n1 | PDB
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| PC cid
PC sid
UniChem
| Article
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| n/a | n/a | 110 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) using ATF-2 as substrate after 1 hr by radiometric based ELISA |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50561020
(CHEMBL4783948) | PDB
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KEGG
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| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 150 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) using ATF-2 as substrate after 1 hr by radiometric based ELISA |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM5446
(CHEMBL553 | ERLOTINIB HYDROCHLORIDE | Erlotinib | ...)Show InChI InChI=1S/C22H23N3O4/c1-4-16-6-5-7-17(12-16)25-22-18-13-20(28-10-8-26-2)21(29-11-9-27-3)14-19(18)23-15-24-22/h1,5-7,12-15H,8-11H2,2-3H3,(H,23,24,25) | PDB
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| DrugBank
MMDB
PDB
Article
PubMed
| n/a | n/a | 153 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) using ATF-2 as substrate after 1 hr by radiometric based ELISA |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50561022
(CHEMBL4740646)Show SMILES COc1ccc(\C=N/Nc2nc(cs2)-c2nc3ccccc3n2C)cc1OC | PDB
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| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 208 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) using ATF-2 as substrate after 1 hr by radiometric based ELISA |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50561029
(CHEMBL4746023) | PDB
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| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 213 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) using ATF-2 as substrate after 1 hr by radiometric based ELISA |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50561026
(CHEMBL4752843)Show SMILES Cn1c(nc2ccccc12)-c1csc(N\N=C/c2ccc(F)cc2)n1 | PDB
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| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 254 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) using ATF-2 as substrate after 1 hr by radiometric based ELISA |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50561018
(CHEMBL4747759)Show SMILES [#6]-n1c(nc2ccccc12)-c1csc(-[#7]\[#7]=[#6]-2\[#6]-[#6]-[#6]-[#6]-[#6]-2)n1 | PDB
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| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 279 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) using ATF-2 as substrate after 1 hr by radiometric based ELISA |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50561021
(CHEMBL4794131) | PDB
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UniChem
| Article
PubMed
| n/a | n/a | 312 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) using ATF-2 as substrate after 1 hr by radiometric based ELISA |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50561032
(CHEMBL4749518) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 342 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) using ATF-2 as substrate after 1 hr by radiometric based ELISA |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50561027
(CHEMBL4746321)Show SMILES Cn1c(nc2ccccc12)-c1csc(N\N=C/c2ccc(Br)cc2)n1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 406 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) using ATF-2 as substrate after 1 hr by radiometric based ELISA |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50561028
(CHEMBL4762604)Show SMILES Cn1c(nc2ccccc12)-c1csc(N\N=C/c2ccc(Cl)cc2Cl)n1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 514 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) using ATF-2 as substrate after 1 hr by radiometric based ELISA |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50561033
(CHEMBL4796408) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 569 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) using ATF-2 as substrate after 1 hr by radiometric based ELISA |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50561023
(CHEMBL4758204)Show SMILES COc1cc(\C=N/Nc2nc(cs2)-c2nc3ccccc3n2C)cc(OC)c1OC | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 623 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) using ATF-2 as substrate after 1 hr by radiometric based ELISA |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50561031
(CHEMBL4763960) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 773 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) using ATF-2 as substrate after 1 hr by radiometric based ELISA |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50561019
(CHEMBL4749342) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 1.24E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of EGFR (unknown origin) using ATF-2 as substrate after 1 hr by radiometric based ELISA |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair | |
DNA topoisomerase 2-alpha
(Homo sapiens (Human)) | BDBM50561016
(CHEMBL34922)Show SMILES Cl.Cl.Cl.CN1CCN(CC1)c1ccc2nc([nH]c2c1)-c1ccc2nc([nH]c2c1)-c1ccc(O)cc1 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 3.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of Topoisomerase 2 (unknown origin) |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair | |
DNA topoisomerase 1
(Homo sapiens (Human)) | BDBM50561016
(CHEMBL34922)Show SMILES Cl.Cl.Cl.CN1CCN(CC1)c1ccc2nc([nH]c2c1)-c1ccc2nc([nH]c2c1)-c1ccc(O)cc1 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 3.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of Topoisomerase 1 (unknown origin) |
Citation and Details
Article DOI: 10.1016/j.bmc.2020.115657
BindingDB Entry DOI: 10.7270/Q21J9FHZ |
More data for this
Ligand-Target Pair | |
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