Found 14 hits Enz. Inhib. hit(s) with all data for entry = 50047183 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)) | BDBM50152685
(CHEMBL3780676)Show SMILES COc1cc2c(Oc3ccc(NC(=O)c4c(Cl)c5ccccc5n(-c5ccc(F)cc5)c4=O)cc3F)ccnc2cc1OCCCN1CCN(C)CC1 Show InChI InChI=1S/C40H36ClF2N5O5/c1-46-17-19-47(20-18-46)16-5-21-52-36-24-31-29(23-35(36)51-2)33(14-15-44-31)53-34-13-10-26(22-30(34)43)45-39(49)37-38(41)28-6-3-4-7-32(28)48(40(37)50)27-11-8-25(42)9-12-27/h3-4,6-15,22-24H,5,16-21H2,1-2H3,(H,45,49) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.20 | n/a | n/a | n/a | n/a | n/a | n/a |
Jiangxi Science and Technology Normal University
Curated by ChEMBL
| Assay Description
Inhibition of cMet (unknown origin) using poly (Glu, Tyr) 4:1 as substrate after 30 mins by HTRF assay |
Bioorg Med Chem Lett 26: 1794-8 (2016)
Article DOI: 10.1016/j.bmcl.2016.02.037
BindingDB Entry DOI: 10.7270/Q2TT4ST4 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50152684
(CHEMBL3781716)Show SMILES COc1cc2c(Oc3ccc(NC(=O)c4c(Cl)c5ccccc5n(-c5ccccc5)c4=O)cc3F)ccnc2cc1OCCCN1CCN(C)CC1 Show InChI InChI=1S/C40H37ClFN5O5/c1-45-18-20-46(21-19-45)17-8-22-51-36-25-31-29(24-35(36)50-2)33(15-16-43-31)52-34-14-13-26(23-30(34)42)44-39(48)37-38(41)28-11-6-7-12-32(28)47(40(37)49)27-9-4-3-5-10-27/h3-7,9-16,23-25H,8,17-22H2,1-2H3,(H,44,48) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.80 | n/a | n/a | n/a | n/a | n/a | n/a |
Jiangxi Science and Technology Normal University
Curated by ChEMBL
| Assay Description
Inhibition of cMet (unknown origin) using poly (Glu, Tyr) 4:1 as substrate after 30 mins by HTRF assay |
Bioorg Med Chem Lett 26: 1794-8 (2016)
Article DOI: 10.1016/j.bmcl.2016.02.037
BindingDB Entry DOI: 10.7270/Q2TT4ST4 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50399540
(FORETINIB | US10464902, Foretinib | US10882853, Co...)Show SMILES COc1cc2c(Oc3ccc(NC(=O)C4(CC4)C(=O)Nc4ccc(F)cc4)cc3F)ccnc2cc1OCCCN1CCOCC1 Show InChI InChI=1S/C34H34F2N4O6/c1-43-30-20-25-27(21-31(30)45-16-2-13-40-14-17-44-18-15-40)37-12-9-28(25)46-29-8-7-24(19-26(29)36)39-33(42)34(10-11-34)32(41)38-23-5-3-22(35)4-6-23/h3-9,12,19-21H,2,10-11,13-18H2,1H3,(H,38,41)(H,39,42) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Similars
| PDB
Article
PubMed
| n/a | n/a | 1.80 | n/a | n/a | n/a | n/a | n/a | n/a |
Jiangxi Science and Technology Normal University
Curated by ChEMBL
| Assay Description
Inhibition of cMet (unknown origin) using poly (Glu, Tyr) 4:1 as substrate after 30 mins by HTRF assay |
Bioorg Med Chem Lett 26: 1794-8 (2016)
Article DOI: 10.1016/j.bmcl.2016.02.037
BindingDB Entry DOI: 10.7270/Q2TT4ST4 |
More data for this
Ligand-Target Pair | 
3D Structure (crystal) |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50152685
(CHEMBL3780676)Show SMILES COc1cc2c(Oc3ccc(NC(=O)c4c(Cl)c5ccccc5n(-c5ccc(F)cc5)c4=O)cc3F)ccnc2cc1OCCCN1CCN(C)CC1 Show InChI InChI=1S/C40H36ClF2N5O5/c1-46-17-19-47(20-18-46)16-5-21-52-36-24-31-29(23-35(36)51-2)33(14-15-44-31)53-34-13-10-26(22-30(34)43)45-39(49)37-38(41)28-6-3-4-7-32(28)48(40(37)50)27-11-8-25(42)9-12-27/h3-4,6-15,22-24H,5,16-21H2,1-2H3,(H,45,49) | PDB
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 | 2.20 | n/a | n/a | n/a | n/a | n/a | n/a |
Jiangxi Science and Technology Normal University
Curated by ChEMBL
| Assay Description
Inhibition of FLT3 (unknown origin) using poly (Glu, Tyr) 4:1 as substrate after 30 mins by HTRF assay |
Bioorg Med Chem Lett 26: 1794-8 (2016)
Article DOI: 10.1016/j.bmcl.2016.02.037
BindingDB Entry DOI: 10.7270/Q2TT4ST4 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50152683
(CHEMBL3781674)Show SMILES COc1cc2c(Oc3ccc(NC(=O)c4c(Cl)c5ccccc5n(-c5ccc(F)cc5)c4=O)cc3F)ccnc2cc1OCCCN1CCC(C)CC1 Show InChI InChI=1S/C41H37ClF2N4O5/c1-25-15-19-47(20-16-25)18-5-21-52-37-24-32-30(23-36(37)51-2)34(14-17-45-32)53-35-13-10-27(22-31(35)44)46-40(49)38-39(42)29-6-3-4-7-33(29)48(41(38)50)28-11-8-26(43)9-12-28/h3-4,6-14,17,22-25H,5,15-16,18-21H2,1-2H3,(H,46,49) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 3.30 | n/a | n/a | n/a | n/a | n/a | n/a |
Jiangxi Science and Technology Normal University
Curated by ChEMBL
| Assay Description
Inhibition of cMet (unknown origin) using poly (Glu, Tyr) 4:1 as substrate after 30 mins by HTRF assay |
Bioorg Med Chem Lett 26: 1794-8 (2016)
Article DOI: 10.1016/j.bmcl.2016.02.037
BindingDB Entry DOI: 10.7270/Q2TT4ST4 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50152678
(CHEMBL3780761)Show SMILES COc1cc2c(Oc3ccc(NC(=O)c4c(Cl)c5ccccc5n(-c5ccc(F)cc5)c4=O)cc3F)ccnc2cc1OCCCN1CCOCC1 Show InChI InChI=1S/C39H33ClF2N4O6/c1-49-34-22-28-30(23-35(34)51-18-4-15-45-16-19-50-20-17-45)43-14-13-32(28)52-33-12-9-25(21-29(33)42)44-38(47)36-37(40)27-5-2-3-6-31(27)46(39(36)48)26-10-7-24(41)8-11-26/h2-3,5-14,21-23H,4,15-20H2,1H3,(H,44,47) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 5.30 | n/a | n/a | n/a | n/a | n/a | n/a |
Jiangxi Science and Technology Normal University
Curated by ChEMBL
| Assay Description
Inhibition of cMet (unknown origin) using poly (Glu, Tyr) 4:1 as substrate after 30 mins by HTRF assay |
Bioorg Med Chem Lett 26: 1794-8 (2016)
Article DOI: 10.1016/j.bmcl.2016.02.037
BindingDB Entry DOI: 10.7270/Q2TT4ST4 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50152682
(CHEMBL3780662)Show SMILES COc1cc2c(Oc3ccc(NC(=O)c4c(Cl)c5ccccc5n(-c5ccccc5)c4=O)cc3F)ccnc2cc1OCCCN1CCC(C)CC1 Show InChI InChI=1S/C41H38ClFN4O5/c1-26-16-20-46(21-17-26)19-8-22-51-37-25-32-30(24-36(37)50-2)34(15-18-44-32)52-35-14-13-27(23-31(35)43)45-40(48)38-39(42)29-11-6-7-12-33(29)47(41(38)49)28-9-4-3-5-10-28/h3-7,9-15,18,23-26H,8,16-17,19-22H2,1-2H3,(H,45,48) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 6.80 | n/a | n/a | n/a | n/a | n/a | n/a |
Jiangxi Science and Technology Normal University
Curated by ChEMBL
| Assay Description
Inhibition of cMet (unknown origin) using poly (Glu, Tyr) 4:1 as substrate after 30 mins by HTRF assay |
Bioorg Med Chem Lett 26: 1794-8 (2016)
Article DOI: 10.1016/j.bmcl.2016.02.037
BindingDB Entry DOI: 10.7270/Q2TT4ST4 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50152681
(CHEMBL3781197)Show SMILES COc1cc2c(Oc3ccc(NC(=O)c4c(Cl)c5ccccc5n(-c5ccc(F)cc5)c4=O)cc3F)ccnc2cc1OCCCN1CCCCC1 Show InChI InChI=1S/C40H35ClF2N4O5/c1-50-35-23-29-31(24-36(35)51-21-7-20-46-18-5-2-6-19-46)44-17-16-33(29)52-34-15-12-26(22-30(34)43)45-39(48)37-38(41)28-8-3-4-9-32(28)47(40(37)49)27-13-10-25(42)11-14-27/h3-4,8-17,22-24H,2,5-7,18-21H2,1H3,(H,45,48) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 12 | n/a | n/a | n/a | n/a | n/a | n/a |
Jiangxi Science and Technology Normal University
Curated by ChEMBL
| Assay Description
Inhibition of cMet (unknown origin) using poly (Glu, Tyr) 4:1 as substrate after 30 mins by HTRF assay |
Bioorg Med Chem Lett 26: 1794-8 (2016)
Article DOI: 10.1016/j.bmcl.2016.02.037
BindingDB Entry DOI: 10.7270/Q2TT4ST4 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50152679
(CHEMBL3780556)Show SMILES COc1cc2c(Oc3ccc(NC(=O)c4c(Cl)c5ccccc5n(-c5ccc(F)cc5)c4=O)cc3F)ccnc2cc1OCCCN1CCCC1 Show InChI InChI=1S/C39H33ClF2N4O5/c1-49-34-22-28-30(23-35(34)50-20-6-19-45-17-4-5-18-45)43-16-15-32(28)51-33-14-11-25(21-29(33)42)44-38(47)36-37(40)27-7-2-3-8-31(27)46(39(36)48)26-12-9-24(41)10-13-26/h2-3,7-16,21-23H,4-6,17-20H2,1H3,(H,44,47) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 13 | n/a | n/a | n/a | n/a | n/a | n/a |
Jiangxi Science and Technology Normal University
Curated by ChEMBL
| Assay Description
Inhibition of cMet (unknown origin) using poly (Glu, Tyr) 4:1 as substrate after 30 mins by HTRF assay |
Bioorg Med Chem Lett 26: 1794-8 (2016)
Article DOI: 10.1016/j.bmcl.2016.02.037
BindingDB Entry DOI: 10.7270/Q2TT4ST4 |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50152680
(CHEMBL3780566)Show SMILES COc1cc2c(Oc3ccc(NC(=O)c4c(Cl)c5ccccc5n(-c5ccccc5)c4=O)cc3F)ccnc2cc1OCCCN1CCCCC1 Show InChI InChI=1S/C40H36ClFN4O5/c1-49-35-24-29-31(25-36(35)50-22-10-21-45-19-8-3-9-20-45)43-18-17-33(29)51-34-16-15-26(23-30(34)42)44-39(47)37-38(41)28-13-6-7-14-32(28)46(40(37)48)27-11-4-2-5-12-27/h2,4-7,11-18,23-25H,3,8-10,19-22H2,1H3,(H,44,47) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 18 | n/a | n/a | n/a | n/a | n/a | n/a |
Jiangxi Science and Technology Normal University
Curated by ChEMBL
| Assay Description
Inhibition of cMet (unknown origin) using poly (Glu, Tyr) 4:1 as substrate after 30 mins by HTRF assay |
Bioorg Med Chem Lett 26: 1794-8 (2016)
Article DOI: 10.1016/j.bmcl.2016.02.037
BindingDB Entry DOI: 10.7270/Q2TT4ST4 |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50152685
(CHEMBL3780676)Show SMILES COc1cc2c(Oc3ccc(NC(=O)c4c(Cl)c5ccccc5n(-c5ccc(F)cc5)c4=O)cc3F)ccnc2cc1OCCCN1CCN(C)CC1 Show InChI InChI=1S/C40H36ClF2N5O5/c1-46-17-19-47(20-18-46)16-5-21-52-36-24-31-29(23-35(36)51-2)33(14-15-44-31)53-34-13-10-26(22-30(34)43)45-39(49)37-38(41)28-6-3-4-7-32(28)48(40(37)50)27-11-8-25(42)9-12-27/h3-4,6-15,22-24H,5,16-21H2,1-2H3,(H,45,49) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 363 | n/a | n/a | n/a | n/a | n/a | n/a |
Jiangxi Science and Technology Normal University
Curated by ChEMBL
| Assay Description
Inhibition of cKIT (unknown origin) using poly (Glu, Tyr) 4:1 as substrate after 30 mins by HTRF assay |
Bioorg Med Chem Lett 26: 1794-8 (2016)
Article DOI: 10.1016/j.bmcl.2016.02.037
BindingDB Entry DOI: 10.7270/Q2TT4ST4 |
More data for this
Ligand-Target Pair | |
Platelet-derived growth factor receptor beta
(Homo sapiens (Human)) | BDBM50152685
(CHEMBL3780676)Show SMILES COc1cc2c(Oc3ccc(NC(=O)c4c(Cl)c5ccccc5n(-c5ccc(F)cc5)c4=O)cc3F)ccnc2cc1OCCCN1CCN(C)CC1 Show InChI InChI=1S/C40H36ClF2N5O5/c1-46-17-19-47(20-18-46)16-5-21-52-36-24-31-29(23-35(36)51-2)33(14-15-44-31)53-34-13-10-26(22-30(34)43)45-39(49)37-38(41)28-6-3-4-7-32(28)48(40(37)50)27-11-8-25(42)9-12-27/h3-4,6-15,22-24H,5,16-21H2,1-2H3,(H,45,49) | 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 | 527 | n/a | n/a | n/a | n/a | n/a | n/a |
Jiangxi Science and Technology Normal University
Curated by ChEMBL
| Assay Description
Inhibition of PDGFRbeta (unknown origin) using poly (Glu, Tyr) 4:1 as substrate after 30 mins by HTRF assay |
Bioorg Med Chem Lett 26: 1794-8 (2016)
Article DOI: 10.1016/j.bmcl.2016.02.037
BindingDB Entry DOI: 10.7270/Q2TT4ST4 |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50152685
(CHEMBL3780676)Show SMILES COc1cc2c(Oc3ccc(NC(=O)c4c(Cl)c5ccccc5n(-c5ccc(F)cc5)c4=O)cc3F)ccnc2cc1OCCCN1CCN(C)CC1 Show InChI InChI=1S/C40H36ClF2N5O5/c1-46-17-19-47(20-18-46)16-5-21-52-36-24-31-29(23-35(36)51-2)33(14-15-44-31)53-34-13-10-26(22-30(34)43)45-39(49)37-38(41)28-6-3-4-7-32(28)48(40(37)50)27-11-8-25(42)9-12-27/h3-4,6-15,22-24H,5,16-21H2,1-2H3,(H,45,49) | 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 | 543 | n/a | n/a | n/a | n/a | n/a | n/a |
Jiangxi Science and Technology Normal University
Curated by ChEMBL
| Assay Description
Inhibition of VEGFR-2 (unknown origin) using poly (Glu, Tyr) 4:1 as substrate after 30 mins by HTRF assay |
Bioorg Med Chem Lett 26: 1794-8 (2016)
Article DOI: 10.1016/j.bmcl.2016.02.037
BindingDB Entry DOI: 10.7270/Q2TT4ST4 |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50152685
(CHEMBL3780676)Show SMILES COc1cc2c(Oc3ccc(NC(=O)c4c(Cl)c5ccccc5n(-c5ccc(F)cc5)c4=O)cc3F)ccnc2cc1OCCCN1CCN(C)CC1 Show InChI InChI=1S/C40H36ClF2N5O5/c1-46-17-19-47(20-18-46)16-5-21-52-36-24-31-29(23-35(36)51-2)33(14-15-44-31)53-34-13-10-26(22-30(34)43)45-39(49)37-38(41)28-6-3-4-7-32(28)48(40(37)50)27-11-8-25(42)9-12-27/h3-4,6-15,22-24H,5,16-21H2,1-2H3,(H,45,49) | 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+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Jiangxi Science and Technology Normal University
Curated by ChEMBL
| Assay Description
Inhibition of EGFR (unknown origin) using poly (Glu, Tyr) 4:1 as substrate after 30 mins by HTRF assay |
Bioorg Med Chem Lett 26: 1794-8 (2016)
Article DOI: 10.1016/j.bmcl.2016.02.037
BindingDB Entry DOI: 10.7270/Q2TT4ST4 |
More data for this
Ligand-Target Pair | |
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