Found 50 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 |
|---|
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50243125
(CHEMBL487864 | N3-(6-acetamidopyridin-3-yl)-4-meth...)Show SMILES CC(=O)Nc1ccc(NC(=O)c2cc(ccc2C)C(=O)Nc2cccc(c2)C(F)(F)F)cn1 Show InChI InChI=1S/C23H19F3N4O3/c1-13-6-7-15(21(32)29-17-5-3-4-16(11-17)23(24,25)26)10-19(13)22(33)30-18-8-9-20(27-12-18)28-14(2)31/h3-12H,1-2H3,(H,29,32)(H,30,33)(H,27,28,31) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet 
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of c-kit (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM26365
(3-N-(2-aminopyrimidin-5-yl)-4-methyl-1-N-[3-(trifl...)Show SMILES Cc1ccc(cc1C(=O)Nc1cnc(N)nc1)C(=O)Nc1cccc(c1)C(F)(F)F Show InChI InChI=1S/C20H16F3N5O2/c1-11-5-6-12(7-16(11)18(30)28-15-9-25-19(24)26-10-15)17(29)27-14-4-2-3-13(8-14)20(21,22)23/h2-10H,1H3,(H,27,29)(H,28,30)(H2,24,25,26) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 5 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of c-kit (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50243076
(CHEMBL470483 | N3-(6-aminopyridin-3-yl)-4-methyl-N...)Show SMILES Cc1ccc(cc1C(=O)Nc1ccc(N)nc1)C(=O)Nc1cccc(c1)C(F)(F)F Show InChI InChI=1S/C21H17F3N4O2/c1-12-5-6-13(9-17(12)20(30)28-16-7-8-18(25)26-11-16)19(29)27-15-4-2-3-14(10-15)21(22,23)24/h2-11H,1H3,(H2,25,26)(H,27,29)(H,28,30) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 7 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of c-kit (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50243181
(CHEMBL520718 | N3-(6-aminopyridin-3-yl)-N1-(3-cycl...)Show SMILES Cc1ccc(cc1C(=O)Nc1ccc(N)nc1)C(=O)NCCCC1CCCCC1 Show InChI InChI=1S/C23H30N4O2/c1-16-9-10-18(22(28)25-13-5-8-17-6-3-2-4-7-17)14-20(16)23(29)27-19-11-12-21(24)26-15-19/h9-12,14-15,17H,2-8,13H2,1H3,(H2,24,26)(H,25,28)(H,27,29) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 9 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of c-kit (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM26373
(4-methyl-3-N-(pyrimidin-5-yl)-1-N-[3-(trifluoromet...)Show SMILES Cc1ccc(NC(=O)c2cccc(c2)C(F)(F)F)cc1C(=O)Nc1cncnc1 Show InChI InChI=1S/C20H15F3N4O2/c1-12-5-6-15(8-17(12)19(29)27-16-9-24-11-25-10-16)26-18(28)13-3-2-4-14(7-13)20(21,22)23/h2-11H,1H3,(H,26,28)(H,27,29) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 14 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of c-kit (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50243075
(4-methyl-N3-(pyridin-3-yl)-N1-(3-(trifluoromethyl)...)Show SMILES Cc1ccc(cc1C(=O)Nc1cccnc1)C(=O)Nc1cccc(c1)C(F)(F)F Show InChI InChI=1S/C21H16F3N3O2/c1-13-7-8-14(10-18(13)20(29)27-17-6-3-9-25-12-17)19(28)26-16-5-2-4-15(11-16)21(22,23)24/h2-12H,1H3,(H,26,28)(H,27,29) | PDB
UniProtKB/SwissProt
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 |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of c-kit (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM50243076
(CHEMBL470483 | N3-(6-aminopyridin-3-yl)-4-methyl-N...)Show SMILES Cc1ccc(cc1C(=O)Nc1ccc(N)nc1)C(=O)Nc1cccc(c1)C(F)(F)F Show InChI InChI=1S/C21H17F3N4O2/c1-12-5-6-13(9-17(12)20(30)28-16-7-8-18(25)26-11-16)19(29)27-15-4-2-3-14(10-15)21(22,23)24/h2-11H,1H3,(H2,25,26)(H,27,29)(H,28,30) | 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 | 24 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of p38alpha (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50243180
(CHEMBL488834 | N3-(6-aminopyridin-3-yl)-N1-(2-cycl...)Show SMILES Cc1ccc(cc1C(=O)Nc1ccc(N)nc1)C(=O)NCCC1CCCCC1 Show InChI InChI=1S/C22H28N4O2/c1-15-7-8-17(21(27)24-12-11-16-5-3-2-4-6-16)13-19(15)22(28)26-18-9-10-20(23)25-14-18/h7-10,13-14,16H,2-6,11-12H2,1H3,(H2,23,25)(H,24,27)(H,26,28) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 35 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of c-kit (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50242924
(4-methyl-N3-(pyrimidin-5-yl)-N1-(3-(trifluoromethy...)Show SMILES Cc1ccc(cc1C(=O)Nc1cncnc1)C(=O)Nc1cccc(c1)C(F)(F)F Show InChI InChI=1S/C20H15F3N4O2/c1-12-5-6-13(7-17(12)19(29)27-16-9-24-11-25-10-16)18(28)26-15-4-2-3-14(8-15)20(21,22)23/h2-11H,1H3,(H,26,28)(H,27,29) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 37 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of c-kit (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM50243125
(CHEMBL487864 | N3-(6-acetamidopyridin-3-yl)-4-meth...)Show SMILES CC(=O)Nc1ccc(NC(=O)c2cc(ccc2C)C(=O)Nc2cccc(c2)C(F)(F)F)cn1 Show InChI InChI=1S/C23H19F3N4O3/c1-13-6-7-15(21(32)29-17-5-3-4-16(11-17)23(24,25)26)10-19(13)22(33)30-18-8-9-20(27-12-18)28-14(2)31/h3-12H,1-2H3,(H,29,32)(H,30,33)(H,27,28,31) | 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 | 45 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of p38alpha (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM13530
(4-[(4-methylpiperazin-1-yl)methyl]-N-[4-methyl-3-[...)Show SMILES CN1CCN(Cc2ccc(cc2)C(=O)Nc2ccc(C)c(Nc3nccc(n3)-c3cccnc3)c2)CC1 Show InChI InChI=1S/C29H31N7O/c1-21-5-10-25(18-27(21)34-29-31-13-11-26(33-29)24-4-3-12-30-19-24)32-28(37)23-8-6-22(7-9-23)20-36-16-14-35(2)15-17-36/h3-13,18-19H,14-17,20H2,1-2H3,(H,32,37)(H,31,33,34) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 52 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of c-kit (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM50243181
(CHEMBL520718 | N3-(6-aminopyridin-3-yl)-N1-(3-cycl...)Show SMILES Cc1ccc(cc1C(=O)Nc1ccc(N)nc1)C(=O)NCCCC1CCCCC1 Show InChI InChI=1S/C23H30N4O2/c1-16-9-10-18(22(28)25-13-5-8-17-6-3-2-4-7-17)14-20(16)23(29)27-19-11-12-21(24)26-15-19/h9-12,14-15,17H,2-8,13H2,1H3,(H2,24,26)(H,25,28)(H,27,29) | 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 | 57.8 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of p38alpha (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50243124
(CHEMBL487863 | N3-(2-acetamidopyrimidin-5-yl)-4-me...)Show SMILES CC(=O)Nc1ncc(NC(=O)c2cc(ccc2C)C(=O)Nc2cccc(c2)C(F)(F)F)cn1 Show InChI InChI=1S/C22H18F3N5O3/c1-12-6-7-14(19(32)29-16-5-3-4-15(9-16)22(23,24)25)8-18(12)20(33)30-17-10-26-21(27-11-17)28-13(2)31/h3-11H,1-2H3,(H,29,32)(H,30,33)(H,26,27,28,31) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 58 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of c-kit (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50243182
(CHEMBL487431 | N'-(6-aminopyridin-3-yl)-N-(2-cyclo...)Show SMILES Cc1ccc(cc1C(=O)Nc1ccc(N)nc1)C(=O)NCCC1CCCC1 Show InChI InChI=1S/C21H26N4O2/c1-14-6-7-16(20(26)23-11-10-15-4-2-3-5-15)12-18(14)21(27)25-17-8-9-19(22)24-13-17/h6-9,12-13,15H,2-5,10-11H2,1H3,(H2,22,24)(H,23,26)(H,25,27) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 77 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of c-kit (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM26365
(3-N-(2-aminopyrimidin-5-yl)-4-methyl-1-N-[3-(trifl...)Show SMILES Cc1ccc(cc1C(=O)Nc1cnc(N)nc1)C(=O)Nc1cccc(c1)C(F)(F)F Show InChI InChI=1S/C20H16F3N5O2/c1-11-5-6-12(7-16(11)18(30)28-15-9-25-19(24)26-10-15)17(29)27-14-4-2-3-13(8-14)20(21,22)23/h2-10H,1H3,(H,27,29)(H,28,30)(H2,24,25,26) | 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 | 87 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of p38alpha (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50243074
(CHEMBL469882 | N-(2-methyl-5-((3-(trifluoromethyl)...)Show SMILES Cc1ccc(cc1NC(=O)c1cncnc1)C(=O)Nc1cccc(c1)C(F)(F)F Show InChI InChI=1S/C20H15F3N4O2/c1-12-5-6-13(7-17(12)27-19(29)14-9-24-11-25-10-14)18(28)26-16-4-2-3-15(8-16)20(21,22)23/h2-11H,1H3,(H,26,28)(H,27,29) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 108 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of c-kit (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase ABL1
(Homo sapiens (Human)) | BDBM13530
(4-[(4-methylpiperazin-1-yl)methyl]-N-[4-methyl-3-[...)Show SMILES CN1CCN(Cc2ccc(cc2)C(=O)Nc2ccc(C)c(Nc3nccc(n3)-c3cccnc3)c2)CC1 Show InChI InChI=1S/C29H31N7O/c1-21-5-10-25(18-27(21)34-29-31-13-11-26(33-29)24-4-3-12-30-19-24)32-28(37)23-8-6-22(7-9-23)20-36-16-14-35(2)15-17-36/h3-13,18-19H,14-17,20H2,1-2H3,(H,32,37)(H,31,33,34) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| DrugBank
PDB
Article
PubMed
| n/a | n/a | 110 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of Abl (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | 
3D Structure (crystal) |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50243125
(CHEMBL487864 | N3-(6-acetamidopyridin-3-yl)-4-meth...)Show SMILES CC(=O)Nc1ccc(NC(=O)c2cc(ccc2C)C(=O)Nc2cccc(c2)C(F)(F)F)cn1 Show InChI InChI=1S/C23H19F3N4O3/c1-13-6-7-15(21(32)29-17-5-3-4-16(11-17)23(24,25)26)10-19(13)22(33)30-18-8-9-20(27-12-18)28-14(2)31/h3-12H,1-2H3,(H,29,32)(H,30,33)(H,27,28,31) | 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 | 114 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of KDR (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50243126
(CHEMBL487865 | N3-(6-aminopyridin-3-yl)-4-methyl-N...)Show SMILES Cc1ccc(cc1C(=O)Nc1ccc(N)nc1)C(=O)Nc1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C21H17F3N4O2/c1-12-2-3-13(10-17(12)20(30)28-16-8-9-18(25)26-11-16)19(29)27-15-6-4-14(5-7-15)21(22,23)24/h2-11H,1H3,(H2,25,26)(H,27,29)(H,28,30) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 120 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of c-kit (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM50243180
(CHEMBL488834 | N3-(6-aminopyridin-3-yl)-N1-(2-cycl...)Show SMILES Cc1ccc(cc1C(=O)Nc1ccc(N)nc1)C(=O)NCCC1CCCCC1 Show InChI InChI=1S/C22H28N4O2/c1-15-7-8-17(21(27)24-12-11-16-5-3-2-4-6-16)13-19(15)22(28)26-18-9-10-20(23)25-14-18/h7-10,13-14,16H,2-6,11-12H2,1H3,(H2,23,25)(H,24,27)(H,26,28) | 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 | 181 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of p38alpha (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM26373
(4-methyl-3-N-(pyrimidin-5-yl)-1-N-[3-(trifluoromet...)Show SMILES Cc1ccc(NC(=O)c2cccc(c2)C(F)(F)F)cc1C(=O)Nc1cncnc1 Show InChI InChI=1S/C20H15F3N4O2/c1-12-5-6-15(8-17(12)19(29)27-16-9-24-11-25-10-16)26-18(28)13-3-2-4-14(7-13)20(21,22)23/h2-11H,1H3,(H,26,28)(H,27,29) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 200 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of p38alpha (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM26365
(3-N-(2-aminopyrimidin-5-yl)-4-methyl-1-N-[3-(trifl...)Show SMILES Cc1ccc(cc1C(=O)Nc1cnc(N)nc1)C(=O)Nc1cccc(c1)C(F)(F)F Show InChI InChI=1S/C20H16F3N5O2/c1-11-5-6-12(7-16(11)18(30)28-15-9-25-19(24)26-10-15)17(29)27-14-4-2-3-13(8-14)20(21,22)23/h2-10H,1H3,(H,27,29)(H,28,30)(H2,24,25,26) | 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 | 205 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of KDR (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM50243075
(4-methyl-N3-(pyridin-3-yl)-N1-(3-(trifluoromethyl)...)Show SMILES Cc1ccc(cc1C(=O)Nc1cccnc1)C(=O)Nc1cccc(c1)C(F)(F)F Show InChI InChI=1S/C21H16F3N3O2/c1-13-7-8-14(10-18(13)20(29)27-17-6-3-9-25-12-17)19(28)26-16-5-2-4-15(11-16)21(22,23)24/h2-12H,1H3,(H,26,28)(H,27,29) | 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 | 219 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of p38alpha (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM26373
(4-methyl-3-N-(pyrimidin-5-yl)-1-N-[3-(trifluoromet...)Show SMILES Cc1ccc(NC(=O)c2cccc(c2)C(F)(F)F)cc1C(=O)Nc1cncnc1 Show InChI InChI=1S/C20H15F3N4O2/c1-12-5-6-15(8-17(12)19(29)27-16-9-24-11-25-10-16)26-18(28)13-3-2-4-14(7-13)20(21,22)23/h2-11H,1H3,(H,26,28)(H,27,29) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 240 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of Src (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase ABL1
(Homo sapiens (Human)) | BDBM26373
(4-methyl-3-N-(pyrimidin-5-yl)-1-N-[3-(trifluoromet...)Show SMILES Cc1ccc(NC(=O)c2cccc(c2)C(F)(F)F)cc1C(=O)Nc1cncnc1 Show InChI InChI=1S/C20H15F3N4O2/c1-12-5-6-15(8-17(12)19(29)27-16-9-24-11-25-10-16)26-18(28)13-3-2-4-14(7-13)20(21,22)23/h2-11H,1H3,(H,26,28)(H,27,29) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 240 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of Abl (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM26373
(4-methyl-3-N-(pyrimidin-5-yl)-1-N-[3-(trifluoromet...)Show SMILES Cc1ccc(NC(=O)c2cccc(c2)C(F)(F)F)cc1C(=O)Nc1cncnc1 Show InChI InChI=1S/C20H15F3N4O2/c1-12-5-6-15(8-17(12)19(29)27-16-9-24-11-25-10-16)26-18(28)13-3-2-4-14(7-13)20(21,22)23/h2-11H,1H3,(H,26,28)(H,27,29) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 240 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of Lck (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50243075
(4-methyl-N3-(pyridin-3-yl)-N1-(3-(trifluoromethyl)...)Show SMILES Cc1ccc(cc1C(=O)Nc1cccnc1)C(=O)Nc1cccc(c1)C(F)(F)F Show InChI InChI=1S/C21H16F3N3O2/c1-13-7-8-14(10-18(13)20(29)27-17-6-3-9-25-12-17)19(28)26-16-5-2-4-15(11-16)21(22,23)24/h2-12H,1H3,(H,26,28)(H,27,29) | 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 | 294 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of KDR (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM13530
(4-[(4-methylpiperazin-1-yl)methyl]-N-[4-methyl-3-[...)Show SMILES CN1CCN(Cc2ccc(cc2)C(=O)Nc2ccc(C)c(Nc3nccc(n3)-c3cccnc3)c2)CC1 Show InChI InChI=1S/C29H31N7O/c1-21-5-10-25(18-27(21)34-29-31-13-11-26(33-29)24-4-3-12-30-19-24)32-28(37)23-8-6-22(7-9-23)20-36-16-14-35(2)15-17-36/h3-13,18-19H,14-17,20H2,1-2H3,(H,32,37)(H,31,33,34) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| PDB
Article
PubMed
| n/a | n/a | 320 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of Lck (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM50243074
(CHEMBL469882 | N-(2-methyl-5-((3-(trifluoromethyl)...)Show SMILES Cc1ccc(cc1NC(=O)c1cncnc1)C(=O)Nc1cccc(c1)C(F)(F)F Show InChI InChI=1S/C20H15F3N4O2/c1-12-5-6-13(7-17(12)27-19(29)14-9-24-11-25-10-14)18(28)26-16-4-2-3-15(8-16)20(21,22)23/h2-11H,1H3,(H,26,28)(H,27,29) | 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 | 455 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of p38alpha (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50243076
(CHEMBL470483 | N3-(6-aminopyridin-3-yl)-4-methyl-N...)Show SMILES Cc1ccc(cc1C(=O)Nc1ccc(N)nc1)C(=O)Nc1cccc(c1)C(F)(F)F Show InChI InChI=1S/C21H17F3N4O2/c1-12-5-6-13(9-17(12)20(30)28-16-7-8-18(25)26-11-16)19(29)27-15-4-2-3-14(10-15)21(22,23)24/h2-11H,1H3,(H2,25,26)(H,27,29)(H,28,30) | 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 | 470 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of KDR (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50242924
(4-methyl-N3-(pyrimidin-5-yl)-N1-(3-(trifluoromethy...)Show SMILES Cc1ccc(cc1C(=O)Nc1cncnc1)C(=O)Nc1cccc(c1)C(F)(F)F Show InChI InChI=1S/C20H15F3N4O2/c1-12-5-6-13(7-17(12)19(29)27-16-9-24-11-25-10-16)18(28)26-15-4-2-3-14(8-15)20(21,22)23/h2-11H,1H3,(H,26,28)(H,27,29) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 546 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of Lck (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50243124
(CHEMBL487863 | N3-(2-acetamidopyrimidin-5-yl)-4-me...)Show SMILES CC(=O)Nc1ncc(NC(=O)c2cc(ccc2C)C(=O)Nc2cccc(c2)C(F)(F)F)cn1 Show InChI InChI=1S/C22H18F3N5O3/c1-12-6-7-14(19(32)29-16-5-3-4-15(9-16)22(23,24)25)8-18(12)20(33)30-17-10-26-21(27-11-17)28-13(2)31/h3-11H,1-2H3,(H,29,32)(H,30,33)(H,26,27,28,31) | 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 | 748 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of KDR (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM50243182
(CHEMBL487431 | N'-(6-aminopyridin-3-yl)-N-(2-cyclo...)Show SMILES Cc1ccc(cc1C(=O)Nc1ccc(N)nc1)C(=O)NCCC1CCCC1 Show InChI InChI=1S/C21H26N4O2/c1-14-6-7-16(20(26)23-11-10-15-4-2-3-5-15)12-18(14)21(27)25-17-8-9-19(22)24-13-17/h6-9,12-13,15H,2-5,10-11H2,1H3,(H2,22,24)(H,23,26)(H,25,27) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 998 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of p38alpha (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50243179
(CHEMBL488833 | N3-(6-aminopyridin-3-yl)-N1-(cycloh...)Show SMILES Cc1ccc(cc1C(=O)Nc1ccc(N)nc1)C(=O)NCC1CCCCC1 Show InChI InChI=1S/C21H26N4O2/c1-14-7-8-16(20(26)24-12-15-5-3-2-4-6-15)11-18(14)21(27)25-17-9-10-19(22)23-13-17/h7-11,13,15H,2-6,12H2,1H3,(H2,22,23)(H,24,26)(H,25,27) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.18E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of c-kit (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50242924
(4-methyl-N3-(pyrimidin-5-yl)-N1-(3-(trifluoromethy...)Show SMILES Cc1ccc(cc1C(=O)Nc1cncnc1)C(=O)Nc1cccc(c1)C(F)(F)F Show InChI InChI=1S/C20H15F3N4O2/c1-12-5-6-13(7-17(12)19(29)27-16-9-24-11-25-10-16)18(28)26-15-4-2-3-14(8-15)20(21,22)23/h2-11H,1H3,(H,26,28)(H,27,29) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.21E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of Src (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM50243124
(CHEMBL487863 | N3-(2-acetamidopyrimidin-5-yl)-4-me...)Show SMILES CC(=O)Nc1ncc(NC(=O)c2cc(ccc2C)C(=O)Nc2cccc(c2)C(F)(F)F)cn1 Show InChI InChI=1S/C22H18F3N5O3/c1-12-6-7-14(19(32)29-16-5-3-4-15(9-16)22(23,24)25)8-18(12)20(33)30-17-10-26-21(27-11-17)28-13(2)31/h3-11H,1-2H3,(H,29,32)(H,30,33)(H,26,27,28,31) | 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 | 1.73E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of p38alpha (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM50242924
(4-methyl-N3-(pyrimidin-5-yl)-N1-(3-(trifluoromethy...)Show SMILES Cc1ccc(cc1C(=O)Nc1cncnc1)C(=O)Nc1cccc(c1)C(F)(F)F Show InChI InChI=1S/C20H15F3N4O2/c1-12-5-6-13(7-17(12)19(29)27-16-9-24-11-25-10-16)18(28)26-15-4-2-3-14(8-15)20(21,22)23/h2-11H,1H3,(H,26,28)(H,27,29) | 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 | 1.75E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of p38alpha (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50243074
(CHEMBL469882 | N-(2-methyl-5-((3-(trifluoromethyl)...)Show SMILES Cc1ccc(cc1NC(=O)c1cncnc1)C(=O)Nc1cccc(c1)C(F)(F)F Show InChI InChI=1S/C20H15F3N4O2/c1-12-5-6-13(7-17(12)27-19(29)14-9-24-11-25-10-14)18(28)26-16-4-2-3-15(8-16)20(21,22)23/h2-11H,1H3,(H,26,28)(H,27,29) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.76E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of Lck (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50242924
(4-methyl-N3-(pyrimidin-5-yl)-N1-(3-(trifluoromethy...)Show SMILES Cc1ccc(cc1C(=O)Nc1cncnc1)C(=O)Nc1cccc(c1)C(F)(F)F Show InChI InChI=1S/C20H15F3N4O2/c1-12-5-6-13(7-17(12)19(29)27-16-9-24-11-25-10-16)18(28)26-15-4-2-3-14(8-15)20(21,22)23/h2-11H,1H3,(H,26,28)(H,27,29) | 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 | 3.53E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of KDR (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50243183
(CHEMBL505394 | N3-(6-aminopyridin-3-yl)-4-methyl-N...)Show SMILES Cc1ccc(cc1C(=O)Nc1ccc(N)nc1)C(=O)NCCN1CCCC1 Show InChI InChI=1S/C20H25N5O2/c1-14-4-5-15(19(26)22-8-11-25-9-2-3-10-25)12-17(14)20(27)24-16-6-7-18(21)23-13-16/h4-7,12-13H,2-3,8-11H2,1H3,(H2,21,23)(H,22,26)(H,24,27) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 3.64E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of c-kit (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50243074
(CHEMBL469882 | N-(2-methyl-5-((3-(trifluoromethyl)...)Show SMILES Cc1ccc(cc1NC(=O)c1cncnc1)C(=O)Nc1cccc(c1)C(F)(F)F Show InChI InChI=1S/C20H15F3N4O2/c1-12-5-6-13(7-17(12)27-19(29)14-9-24-11-25-10-14)18(28)26-16-4-2-3-15(8-16)20(21,22)23/h2-11H,1H3,(H,26,28)(H,27,29) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 3.76E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of Src (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50243127
(CHEMBL443902 | N3-(6-aminopyridin-3-yl)-N1-cyclohe...)Show InChI InChI=1S/C20H24N4O2/c1-13-7-8-14(19(25)23-15-5-3-2-4-6-15)11-17(13)20(26)24-16-9-10-18(21)22-12-16/h7-12,15H,2-6H2,1H3,(H2,21,22)(H,23,25)(H,24,26) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 4.47E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of c-kit (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50243126
(CHEMBL487865 | N3-(6-aminopyridin-3-yl)-4-methyl-N...)Show SMILES Cc1ccc(cc1C(=O)Nc1ccc(N)nc1)C(=O)Nc1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C21H17F3N4O2/c1-12-2-3-13(10-17(12)20(30)28-16-8-9-18(25)26-11-16)19(29)27-15-6-4-14(5-7-15)21(22,23)24/h2-11H,1H3,(H2,25,26)(H,27,29)(H,28,30) | 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 | >5.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of KDR (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50243074
(CHEMBL469882 | N-(2-methyl-5-((3-(trifluoromethyl)...)Show SMILES Cc1ccc(cc1NC(=O)c1cncnc1)C(=O)Nc1cccc(c1)C(F)(F)F Show InChI InChI=1S/C20H15F3N4O2/c1-12-5-6-13(7-17(12)27-19(29)14-9-24-11-25-10-14)18(28)26-16-4-2-3-15(8-16)20(21,22)23/h2-11H,1H3,(H,26,28)(H,27,29) | 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 | >5.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of KDR (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50243181
(CHEMBL520718 | N3-(6-aminopyridin-3-yl)-N1-(3-cycl...)Show SMILES Cc1ccc(cc1C(=O)Nc1ccc(N)nc1)C(=O)NCCCC1CCCCC1 Show InChI InChI=1S/C23H30N4O2/c1-16-9-10-18(22(28)25-13-5-8-17-6-3-2-4-7-17)14-20(16)23(29)27-19-11-12-21(24)26-15-19/h9-12,14-15,17H,2-8,13H2,1H3,(H2,24,26)(H,25,28)(H,27,29) | 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 | >5.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of KDR (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM26373
(4-methyl-3-N-(pyrimidin-5-yl)-1-N-[3-(trifluoromet...)Show SMILES Cc1ccc(NC(=O)c2cccc(c2)C(F)(F)F)cc1C(=O)Nc1cncnc1 Show InChI InChI=1S/C20H15F3N4O2/c1-12-5-6-15(8-17(12)19(29)27-16-9-24-11-25-10-16)26-18(28)13-3-2-4-14(7-13)20(21,22)23/h2-11H,1H3,(H,26,28)(H,27,29) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >8.33E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of KDR (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM13530
(4-[(4-methylpiperazin-1-yl)methyl]-N-[4-methyl-3-[...)Show SMILES CN1CCN(Cc2ccc(cc2)C(=O)Nc2ccc(C)c(Nc3nccc(n3)-c3cccnc3)c2)CC1 Show InChI InChI=1S/C29H31N7O/c1-21-5-10-25(18-27(21)34-29-31-13-11-26(33-29)24-4-3-12-30-19-24)32-28(37)23-8-6-22(7-9-23)20-36-16-14-35(2)15-17-36/h3-13,18-19H,14-17,20H2,1-2H3,(H,32,37)(H,31,33,34) | PDB
MMDB
NCI pathway
Reactome pathway
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 | 1.37E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of p38alpha (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50243180
(CHEMBL488834 | N3-(6-aminopyridin-3-yl)-N1-(2-cycl...)Show SMILES Cc1ccc(cc1C(=O)Nc1ccc(N)nc1)C(=O)NCCC1CCCCC1 Show InChI InChI=1S/C22H28N4O2/c1-15-7-8-17(21(27)24-12-11-16-5-3-2-4-6-16)13-19(15)22(28)26-18-9-10-20(23)25-14-18/h7-10,13-14,16H,2-6,11-12H2,1H3,(H2,23,25)(H,24,27)(H,26,28) | 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 | >2.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of KDR (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM13530
(4-[(4-methylpiperazin-1-yl)methyl]-N-[4-methyl-3-[...)Show SMILES CN1CCN(Cc2ccc(cc2)C(=O)Nc2ccc(C)c(Nc3nccc(n3)-c3cccnc3)c2)CC1 Show InChI InChI=1S/C29H31N7O/c1-21-5-10-25(18-27(21)34-29-31-13-11-26(33-29)24-4-3-12-30-19-24)32-28(37)23-8-6-22(7-9-23)20-36-16-14-35(2)15-17-36/h3-13,18-19H,14-17,20H2,1-2H3,(H,32,37)(H,31,33,34) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >2.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of KDR (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50243182
(CHEMBL487431 | N'-(6-aminopyridin-3-yl)-N-(2-cyclo...)Show SMILES Cc1ccc(cc1C(=O)Nc1ccc(N)nc1)C(=O)NCCC1CCCC1 Show InChI InChI=1S/C21H26N4O2/c1-14-6-7-16(20(26)23-11-10-15-4-2-3-5-15)12-18(14)21(27)25-17-8-9-19(22)24-13-17/h6-9,12-13,15H,2-5,10-11H2,1H3,(H2,22,24)(H,23,26)(H,25,27) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| MMDB
PDB
Article
PubMed
| n/a | n/a | >2.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc.
Curated by ChEMBL
| Assay Description
Inhibition of KDR (unknown origin) |
Bioorg Med Chem Lett 18: 4137-41 (2008)
Article DOI: 10.1016/j.bmcl.2008.05.089
BindingDB Entry DOI: 10.7270/Q20001WP |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
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