Found 31 hits of Enzyme Inhibition Constant Data 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 |
|---|
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50306682
((R)-3-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)-5-(1...)Show SMILES C[C@@H](Oc1cc(cnc1N)-c1cnn(c1)C1CCNCC1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H22Cl2FN5O/c1-12(19-16(22)2-3-17(24)20(19)23)30-18-8-13(9-27-21(18)25)14-10-28-29(11-14)15-4-6-26-7-5-15/h2-3,8-12,15,26H,4-7H2,1H3,(H2,25,27)/t12-/m1/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| PDB
Article
PubMed
| n/a | n/a | 1.60 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of c-Met incubated for 60 mins at spectrophotometry |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | 
3D Structure (crystal) |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50390444
(CHEMBL2071457)Show SMILES C[C@H](NC(=O)c1cc(cnc1N)-c1cnn(c1)C1CCOCC1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C22H22Cl2FN5O2/c1-12(19-17(23)2-3-18(25)20(19)24)29-22(31)16-8-13(9-27-21(16)26)14-10-28-30(11-14)15-4-6-32-7-5-15/h2-3,8-12,15H,4-7H2,1H3,(H2,26,27)(H,29,31)/t12-/m0/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 22 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of c-Met incubated for 60 mins at spectrophotometry |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50390444
(CHEMBL2071457)Show SMILES C[C@H](NC(=O)c1cc(cnc1N)-c1cnn(c1)C1CCOCC1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C22H22Cl2FN5O2/c1-12(19-17(23)2-3-18(25)20(19)24)29-22(31)16-8-13(9-27-21(16)26)14-10-28-30(11-14)15-4-6-32-7-5-15/h2-3,8-12,15H,4-7H2,1H3,(H2,26,27)(H,29,31)/t12-/m0/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 99 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of c-Met incubated for 60 mins at spectrophotometry |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase receptor Ret
(Homo sapiens (Human)) | BDBM50390444
(CHEMBL2071457)Show SMILES C[C@H](NC(=O)c1cc(cnc1N)-c1cnn(c1)C1CCOCC1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C22H22Cl2FN5O2/c1-12(19-17(23)2-3-18(25)20(19)24)29-22(31)16-8-13(9-27-21(16)26)14-10-28-30(11-14)15-4-6-32-7-5-15/h2-3,8-12,15H,4-7H2,1H3,(H2,26,27)(H,29,31)/t12-/m0/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 210 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of RET |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50390441
(CHEMBL2071452)Show SMILES CC(NC(=O)c1cc(cnc1N)-c1ccc2NC(=O)Cc2c1)c1c(Cl)ccc(F)c1Cl Show InChI InChI=1S/C22H17Cl2FN4O2/c1-10(19-15(23)3-4-16(25)20(19)24)28-22(31)14-7-13(9-27-21(14)26)11-2-5-17-12(6-11)8-18(30)29-17/h2-7,9-10H,8H2,1H3,(H2,26,27)(H,28,31)(H,29,30) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 210 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of c-Met incubated for 60 mins at spectrophotometry |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50390454
(CHEMBL2071448)Show SMILES CC(NC(=O)c1cc(cnc1N)-c1cnn(C)c1)c1c(Cl)ccc(F)c1Cl Show InChI InChI=1S/C18H16Cl2FN5O/c1-9(15-13(19)3-4-14(21)16(15)20)25-18(27)12-5-10(6-23-17(12)22)11-7-24-26(2)8-11/h3-9H,1-2H3,(H2,22,23)(H,25,27) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 280 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of c-Met incubated for 60 mins at spectrophotometry |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50390455
(CHEMBL2071449)Show SMILES CC(NC(=O)c1cc(cnc1N)-c1cnn(c1)C1CCNCC1)c1c(Cl)ccc(F)c1Cl Show InChI InChI=1S/C22H23Cl2FN6O/c1-12(19-17(23)2-3-18(25)20(19)24)30-22(32)16-8-13(9-28-21(16)26)14-10-29-31(11-14)15-4-6-27-7-5-15/h2-3,8-12,15,27H,4-7H2,1H3,(H2,26,28)(H,30,32) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 320 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of c-Met incubated for 60 mins at spectrophotometry |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50390443
(CHEMBL2071454)Show SMILES CC(NC(=O)c1cc(cnc1N)-c1ccc(OCC(=O)N2CCOCC2)cc1)c1c(Cl)ccc(F)c1Cl Show InChI InChI=1S/C26H25Cl2FN4O4/c1-15(23-20(27)6-7-21(29)24(23)28)32-26(35)19-12-17(13-31-25(19)30)16-2-4-18(5-3-16)37-14-22(34)33-8-10-36-11-9-33/h2-7,12-13,15H,8-11,14H2,1H3,(H2,30,31)(H,32,35) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 340 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of c-Met incubated for 60 mins at spectrophotometry |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50390452
(CHEMBL2071392)Show SMILES Cn1cc(cn1)-c1cnc(N)c(c1)C(=O)NCc1c(F)ccc(F)c1Cl Show InChI InChI=1S/C17H14ClF2N5O/c1-25-8-10(6-24-25)9-4-11(16(21)22-5-9)17(26)23-7-12-13(19)2-3-14(20)15(12)18/h2-6,8H,7H2,1H3,(H2,21,22)(H,23,26) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 410 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of c-Met incubated for 60 mins at spectrophotometry |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50390449
(CHEMBL2071389)Show SMILES Cn1cc(cn1)-c1cnc(N)c(c1)C(=O)NCc1ccc(F)c(F)c1 Show InChI InChI=1S/C17H15F2N5O/c1-24-9-12(8-23-24)11-5-13(16(20)21-7-11)17(25)22-6-10-2-3-14(18)15(19)4-10/h2-5,7-9H,6H2,1H3,(H2,20,21)(H,22,25) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 480 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of c-Met incubated for 60 mins at spectrophotometry |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50390456
(CHEMBL2071451)Show SMILES CC(NC(=O)c1cc(cnc1N)-c1ccc(nc1)N1CCOCC1)c1c(Cl)ccc(F)c1Cl Show InChI InChI=1S/C23H22Cl2FN5O2/c1-13(20-17(24)3-4-18(26)21(20)25)30-23(32)16-10-15(12-29-22(16)27)14-2-5-19(28-11-14)31-6-8-33-9-7-31/h2-5,10-13H,6-9H2,1H3,(H2,27,29)(H,30,32) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 510 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of c-Met incubated for 60 mins at spectrophotometry |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50390453
(CHEMBL2071393)Show SMILES Cn1cc(cn1)-c1cnc(N)c(c1)C(=O)NCc1c(F)ccc(Cl)c1Cl Show InChI InChI=1S/C17H14Cl2FN5O/c1-25-8-10(6-24-25)9-4-11(16(21)22-5-9)17(26)23-7-12-14(20)3-2-13(18)15(12)19/h2-6,8H,7H2,1H3,(H2,21,22)(H,23,26) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 560 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of c-Met incubated for 60 mins at spectrophotometry |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50390447
(CHEMBL2071387)Show SMILES Cn1cc(cn1)-c1cnc(N)c(c1)C(=O)NCc1cc(F)ccc1F Show InChI InChI=1S/C17H15F2N5O/c1-24-9-12(8-23-24)10-5-14(16(20)21-6-10)17(25)22-7-11-4-13(18)2-3-15(11)19/h2-6,8-9H,7H2,1H3,(H2,20,21)(H,22,25) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 600 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of c-Met incubated for 60 mins at spectrophotometry |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50390442
(CHEMBL2071453)Show SMILES CC(NC(=O)c1cc(cnc1N)-c1cncnc1)c1c(Cl)ccc(F)c1Cl Show InChI InChI=1S/C18H14Cl2FN5O/c1-9(15-13(19)2-3-14(21)16(15)20)26-18(27)12-4-10(7-25-17(12)22)11-5-23-8-24-6-11/h2-9H,1H3,(H2,22,25)(H,26,27) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.14E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of c-Met incubated for 60 mins at spectrophotometry |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50390451
(CHEMBL2071391)Show SMILES Cn1cc(cn1)-c1cnc(N)c(c1)C(=O)NCc1c(F)ccc(Cl)c1F Show InChI InChI=1S/C17H14ClF2N5O/c1-25-8-10(6-24-25)9-4-11(16(21)22-5-9)17(26)23-7-12-14(19)3-2-13(18)15(12)20/h2-6,8H,7H2,1H3,(H2,21,22)(H,23,26) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.14E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of c-Met incubated for 60 mins at spectrophotometry |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50390445
(CHEMBL2071385)Show SMILES Cn1cc(cn1)-c1cnc(N)c(c1)C(=O)NCc1cccc(F)c1F Show InChI InChI=1S/C17H15F2N5O/c1-24-9-12(8-23-24)11-5-13(16(20)21-7-11)17(25)22-6-10-3-2-4-14(18)15(10)19/h2-5,7-9H,6H2,1H3,(H2,20,21)(H,22,25) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of c-Met incubated for 60 mins at spectrophotometry |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50390450
(CHEMBL2071390)Show SMILES Cn1cc(cn1)-c1cnc(N)c(c1)C(=O)NCc1c(F)cccc1Cl Show InChI InChI=1S/C17H15ClFN5O/c1-24-9-11(7-23-24)10-5-12(16(20)21-6-10)17(25)22-8-13-14(18)3-2-4-15(13)19/h2-7,9H,8H2,1H3,(H2,20,21)(H,22,25) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of c-Met incubated for 60 mins at spectrophotometry |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Fibroblast growth factor receptor 1
(Homo sapiens (Human)) | BDBM50390444
(CHEMBL2071457)Show SMILES C[C@H](NC(=O)c1cc(cnc1N)-c1cnn(c1)C1CCOCC1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C22H22Cl2FN5O2/c1-12(19-17(23)2-3-18(25)20(19)24)29-22(31)16-8-13(9-27-21(16)26)14-10-28-30(11-14)15-4-6-32-7-5-15/h2-3,8-12,15H,4-7H2,1H3,(H2,26,27)(H,29,31)/t12-/m0/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 3.48E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of FGFR1 |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50390448
(CHEMBL2071388)Show SMILES Cn1cc(cn1)-c1cnc(N)c(c1)C(=O)NCc1cc(F)cc(F)c1 Show InChI InChI=1S/C17H15F2N5O/c1-24-9-12(8-23-24)11-4-15(16(20)21-7-11)17(25)22-6-10-2-13(18)5-14(19)3-10/h2-5,7-9H,6H2,1H3,(H2,20,21)(H,22,25) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 4.11E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of c-Met incubated for 60 mins at spectrophotometry |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase ABL1
(Homo sapiens (Human)) | BDBM50390444
(CHEMBL2071457)Show SMILES C[C@H](NC(=O)c1cc(cnc1N)-c1cnn(c1)C1CCOCC1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C22H22Cl2FN5O2/c1-12(19-17(23)2-3-18(25)20(19)24)29-22(31)16-8-13(9-27-21(16)26)14-10-28-30(11-14)15-4-6-32-7-5-15/h2-3,8-12,15H,4-7H2,1H3,(H2,26,27)(H,29,31)/t12-/m0/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 4.99E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of ABL |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Ephrin type-A receptor 2
(Homo sapiens (Human)) | BDBM50390444
(CHEMBL2071457)Show SMILES C[C@H](NC(=O)c1cc(cnc1N)-c1cnn(c1)C1CCOCC1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C22H22Cl2FN5O2/c1-12(19-17(23)2-3-18(25)20(19)24)29-22(31)16-8-13(9-27-21(16)26)14-10-28-30(11-14)15-4-6-32-7-5-15/h2-3,8-12,15H,4-7H2,1H3,(H2,26,27)(H,29,31)/t12-/m0/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 6.18E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of EPHA2 |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50390446
(CHEMBL2071386)Show SMILES Cn1cc(cn1)-c1cnc(N)c(c1)C(=O)NCc1ccc(F)cc1F Show InChI InChI=1S/C17H15F2N5O/c1-24-9-12(8-23-24)11-4-14(16(20)21-7-11)17(25)22-6-10-2-3-13(18)5-15(10)19/h2-5,7-9H,6H2,1H3,(H2,20,21)(H,22,25) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 7.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of c-Met incubated for 60 mins at spectrophotometry |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50390444
(CHEMBL2071457)Show SMILES C[C@H](NC(=O)c1cc(cnc1N)-c1cnn(c1)C1CCOCC1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C22H22Cl2FN5O2/c1-12(19-17(23)2-3-18(25)20(19)24)29-22(31)16-8-13(9-27-21(16)26)14-10-28-30(11-14)15-4-6-32-7-5-15/h2-3,8-12,15H,4-7H2,1H3,(H2,26,27)(H,29,31)/t12-/m0/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 8.16E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of FLT1 |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Macrophage-stimulating protein receptor
(Homo sapiens (Human)) | BDBM50390444
(CHEMBL2071457)Show SMILES C[C@H](NC(=O)c1cc(cnc1N)-c1cnn(c1)C1CCOCC1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C22H22Cl2FN5O2/c1-12(19-17(23)2-3-18(25)20(19)24)29-22(31)16-8-13(9-27-21(16)26)14-10-28-30(11-14)15-4-6-32-7-5-15/h2-3,8-12,15H,4-7H2,1H3,(H2,26,27)(H,29,31)/t12-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 8.26E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of Ron |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50390444
(CHEMBL2071457)Show SMILES C[C@H](NC(=O)c1cc(cnc1N)-c1cnn(c1)C1CCOCC1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C22H22Cl2FN5O2/c1-12(19-17(23)2-3-18(25)20(19)24)29-22(31)16-8-13(9-27-21(16)26)14-10-28-30(11-14)15-4-6-32-7-5-15/h2-3,8-12,15H,4-7H2,1H3,(H2,26,27)(H,29,31)/t12-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of Axl |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase receptor TYRO3
(Homo sapiens (Human)) | BDBM50390444
(CHEMBL2071457)Show SMILES C[C@H](NC(=O)c1cc(cnc1N)-c1cnn(c1)C1CCOCC1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C22H22Cl2FN5O2/c1-12(19-17(23)2-3-18(25)20(19)24)29-22(31)16-8-13(9-27-21(16)26)14-10-28-30(11-14)15-4-6-32-7-5-15/h2-3,8-12,15H,4-7H2,1H3,(H2,26,27)(H,29,31)/t12-/m0/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of TYRO3 |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50390444
(CHEMBL2071457)Show SMILES C[C@H](NC(=O)c1cc(cnc1N)-c1cnn(c1)C1CCOCC1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C22H22Cl2FN5O2/c1-12(19-17(23)2-3-18(25)20(19)24)29-22(31)16-8-13(9-27-21(16)26)14-10-28-30(11-14)15-4-6-32-7-5-15/h2-3,8-12,15H,4-7H2,1H3,(H2,26,27)(H,29,31)/t12-/m0/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of EGFR |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Receptor tyrosine-protein kinase erbB-4
(Homo sapiens (Human)) | BDBM50390444
(CHEMBL2071457)Show SMILES C[C@H](NC(=O)c1cc(cnc1N)-c1cnn(c1)C1CCOCC1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C22H22Cl2FN5O2/c1-12(19-17(23)2-3-18(25)20(19)24)29-22(31)16-8-13(9-27-21(16)26)14-10-28-30(11-14)15-4-6-32-7-5-15/h2-3,8-12,15H,4-7H2,1H3,(H2,26,27)(H,29,31)/t12-/m0/s1 | PDB
MMDB
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of ERBB4 |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Mer
(Homo sapiens (Human)) | BDBM50390444
(CHEMBL2071457)Show SMILES C[C@H](NC(=O)c1cc(cnc1N)-c1cnn(c1)C1CCOCC1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C22H22Cl2FN5O2/c1-12(19-17(23)2-3-18(25)20(19)24)29-22(31)16-8-13(9-27-21(16)26)14-10-28-30(11-14)15-4-6-32-7-5-15/h2-3,8-12,15H,4-7H2,1H3,(H2,26,27)(H,29,31)/t12-/m0/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of Mer |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50390444
(CHEMBL2071457)Show SMILES C[C@H](NC(=O)c1cc(cnc1N)-c1cnn(c1)C1CCOCC1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C22H22Cl2FN5O2/c1-12(19-17(23)2-3-18(25)20(19)24)29-22(31)16-8-13(9-27-21(16)26)14-10-28-30(11-14)15-4-6-32-7-5-15/h2-3,8-12,15H,4-7H2,1H3,(H2,26,27)(H,29,31)/t12-/m0/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of KDR |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
Receptor tyrosine-protein kinase erbB-2
(Homo sapiens (Human)) | BDBM50390444
(CHEMBL2071457)Show SMILES C[C@H](NC(=O)c1cc(cnc1N)-c1cnn(c1)C1CCOCC1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C22H22Cl2FN5O2/c1-12(19-17(23)2-3-18(25)20(19)24)29-22(31)16-8-13(9-27-21(16)26)14-10-28-30(11-14)15-4-6-32-7-5-15/h2-3,8-12,15H,4-7H2,1H3,(H2,26,27)(H,29,31)/t12-/m0/s1 | PDB
MMDB
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of ERBB2 |
Bioorg Med Chem 20: 5169-80 (2012)
Article DOI: 10.1016/j.bmc.2012.07.007
BindingDB Entry DOI: 10.7270/Q2WH2R32 |
More data for this
Ligand-Target Pair | |
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