Found 100 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 |
|---|
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50209158
(2-(4-methyl-piperazin-1-yl)-N-{3-[5-(3-phenoxy-pro...)Show SMILES CN1CCN(CC(=O)Nc2cccc-3c2Cc2c-3n[nH]c2-c2csc(c2)C#CCOc2ccccc2)CC1 Show InChI InChI=1S/C30H29N5O2S/c1-34-12-14-35(15-13-34)19-28(36)31-27-11-5-10-24-25(27)18-26-29(32-33-30(24)26)21-17-23(38-20-21)9-6-16-37-22-7-3-2-4-8-22/h2-5,7-8,10-11,17,20H,12-16,18-19H2,1H3,(H,31,36)(H,32,33) | 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 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt1 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50209158
(2-(4-methyl-piperazin-1-yl)-N-{3-[5-(3-phenoxy-pro...)Show SMILES CN1CCN(CC(=O)Nc2cccc-3c2Cc2c-3n[nH]c2-c2csc(c2)C#CCOc2ccccc2)CC1 Show InChI InChI=1S/C30H29N5O2S/c1-34-12-14-35(15-13-34)19-28(36)31-27-11-5-10-24-25(27)18-26-29(32-33-30(24)26)21-17-23(38-20-21)9-6-16-37-22-7-3-2-4-8-22/h2-5,7-8,10-11,17,20H,12-16,18-19H2,1H3,(H,31,36)(H,32,33) | 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 | 10 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of KDR by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50209148
(CHEMBL246166 | N-{3-[5-(3-phenoxy-prop-1-ynyl)-thi...)Show SMILES COC(=O)C(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C26H19N3O4S/c1-32-26(31)25(30)27-22-11-5-10-19-20(22)14-21-23(28-29-24(19)21)16-13-18(34-15-16)9-6-12-33-17-7-3-2-4-8-17/h2-5,7-8,10-11,13,15H,12,14H2,1H3,(H,27,30)(H,28,29) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 20 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt1 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50209158
(2-(4-methyl-piperazin-1-yl)-N-{3-[5-(3-phenoxy-pro...)Show SMILES CN1CCN(CC(=O)Nc2cccc-3c2Cc2c-3n[nH]c2-c2csc(c2)C#CCOc2ccccc2)CC1 Show InChI InChI=1S/C30H29N5O2S/c1-34-12-14-35(15-13-34)19-28(36)31-27-11-5-10-24-25(27)18-26-29(32-33-30(24)26)21-17-23(38-20-21)9-6-16-37-22-7-3-2-4-8-22/h2-5,7-8,10-11,17,20H,12-16,18-19H2,1H3,(H,31,36)(H,32,33) | 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 | 22 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt3 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50209143
(2-methoxy-N-(3-thiophen-3-yl-2,4-dihydro-indeno[1,...)Show InChI InChI=1S/C17H15N3O2S/c1-22-8-15(21)18-14-4-2-3-11-12(14)7-13-16(19-20-17(11)13)10-5-6-23-9-10/h2-6,9H,7-8H2,1H3,(H,18,21)(H,19,20) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 30 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt1 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50209148
(CHEMBL246166 | N-{3-[5-(3-phenoxy-prop-1-ynyl)-thi...)Show SMILES COC(=O)C(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C26H19N3O4S/c1-32-26(31)25(30)27-22-11-5-10-19-20(22)14-21-23(28-29-24(19)21)16-13-18(34-15-16)9-6-12-33-17-7-3-2-4-8-17/h2-5,7-8,10-11,13,15H,12,14H2,1H3,(H,27,30)(H,28,29) | 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 | 36 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of KDR by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Macrophage colony-stimulating factor 1 receptor
(Homo sapiens (Human)) | BDBM50209158
(2-(4-methyl-piperazin-1-yl)-N-{3-[5-(3-phenoxy-pro...)Show SMILES CN1CCN(CC(=O)Nc2cccc-3c2Cc2c-3n[nH]c2-c2csc(c2)C#CCOc2ccccc2)CC1 Show InChI InChI=1S/C30H29N5O2S/c1-34-12-14-35(15-13-34)19-28(36)31-27-11-5-10-24-25(27)18-26-29(32-33-30(24)26)21-17-23(38-20-21)9-6-16-37-22-7-3-2-4-8-22/h2-5,7-8,10-11,17,20H,12-16,18-19H2,1H3,(H,31,36)(H,32,33) | PDB
UniProtKB/SwissProt
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 |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of CSF1R by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50209158
(2-(4-methyl-piperazin-1-yl)-N-{3-[5-(3-phenoxy-pro...)Show SMILES CN1CCN(CC(=O)Nc2cccc-3c2Cc2c-3n[nH]c2-c2csc(c2)C#CCOc2ccccc2)CC1 Show InChI InChI=1S/C30H29N5O2S/c1-34-12-14-35(15-13-34)19-28(36)31-27-11-5-10-24-25(27)18-26-29(32-33-30(24)26)21-17-23(38-20-21)9-6-16-37-22-7-3-2-4-8-22/h2-5,7-8,10-11,17,20H,12-16,18-19H2,1H3,(H,31,36)(H,32,33) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 49 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50209151
(CHEMBL247388 | N-(3-thiophen-3-yl-2,4-dihydro-inde...)Show SMILES COC(=O)C(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1 Show InChI InChI=1S/C17H13N3O3S/c1-23-17(22)16(21)18-13-4-2-3-10-11(13)7-12-14(19-20-15(10)12)9-5-6-24-8-9/h2-6,8H,7H2,1H3,(H,18,21)(H,19,20) | 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 | 50 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of KDR by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50209146
(CHEMBL247585 | N-(3-thiophen-3-yl-2,4-dihydro-inde...)Show SMILES O=C(Nc1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1)c1ccccc1 Show InChI InChI=1S/C21H15N3OS/c25-21(13-5-2-1-3-6-13)22-18-8-4-7-15-16(18)11-17-19(23-24-20(15)17)14-9-10-26-12-14/h1-10,12H,11H2,(H,22,25)(H,23,24) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 50 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt1 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50209150
(2-methoxy-N-{3-[5-(3-phenoxy-prop-1-ynyl)-thiophen...)Show SMILES COCC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C26H21N3O3S/c1-31-15-24(30)27-23-11-5-10-20-21(23)14-22-25(28-29-26(20)22)17-13-19(33-16-17)9-6-12-32-18-7-3-2-4-8-18/h2-5,7-8,10-11,13,16H,12,14-15H2,1H3,(H,27,30)(H,28,29) | 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 | 53 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of KDR by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50209154
(5-methyl-isoxazole-3-carboxylic acid (3-thiophen-3...)Show SMILES Cc1cc(no1)C(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1 Show InChI InChI=1S/C19H14N4O2S/c1-10-7-16(23-25-10)19(24)20-15-4-2-3-12-13(15)8-14-17(21-22-18(12)14)11-5-6-26-9-11/h2-7,9H,8H2,1H3,(H,20,24)(H,21,22) | 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 | 60 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of KDR by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50209148
(CHEMBL246166 | N-{3-[5-(3-phenoxy-prop-1-ynyl)-thi...)Show SMILES COC(=O)C(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C26H19N3O4S/c1-32-26(31)25(30)27-22-11-5-10-19-20(22)14-21-23(28-29-24(19)21)16-13-18(34-15-16)9-6-12-33-17-7-3-2-4-8-17/h2-5,7-8,10-11,13,15H,12,14H2,1H3,(H,27,30)(H,28,29) | 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 | 65 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt3 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50209143
(2-methoxy-N-(3-thiophen-3-yl-2,4-dihydro-indeno[1,...)Show InChI InChI=1S/C17H15N3O2S/c1-22-8-15(21)18-14-4-2-3-11-12(14)7-13-16(19-20-17(11)13)10-5-6-23-9-10/h2-6,9H,7-8H2,1H3,(H,18,21)(H,19,20) | 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 | 70 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of KDR by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50209154
(5-methyl-isoxazole-3-carboxylic acid (3-thiophen-3...)Show SMILES Cc1cc(no1)C(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1 Show InChI InChI=1S/C19H14N4O2S/c1-10-7-16(23-25-10)19(24)20-15-4-2-3-12-13(15)8-14-17(21-22-18(12)14)11-5-6-26-9-11/h2-7,9H,8H2,1H3,(H,20,24)(H,21,22) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 70 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt1 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50209151
(CHEMBL247388 | N-(3-thiophen-3-yl-2,4-dihydro-inde...)Show SMILES COC(=O)C(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1 Show InChI InChI=1S/C17H13N3O3S/c1-23-17(22)16(21)18-13-4-2-3-10-11(13)7-12-14(19-20-15(10)12)9-5-6-24-8-9/h2-6,8H,7H2,1H3,(H,18,21)(H,19,20) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 80 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt1 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50209153
(CHEMBL247389 | furan-2-carboxylic acid (3-thiophen...)Show SMILES O=C(Nc1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1)c1ccco1 Show InChI InChI=1S/C19H13N3O2S/c23-19(16-5-2-7-24-16)20-15-4-1-3-12-13(15)9-14-17(21-22-18(12)14)11-6-8-25-10-11/h1-8,10H,9H2,(H,20,23)(H,21,22) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 90 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt1 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50209146
(CHEMBL247585 | N-(3-thiophen-3-yl-2,4-dihydro-inde...)Show SMILES O=C(Nc1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1)c1ccccc1 Show InChI InChI=1S/C21H15N3OS/c25-21(13-5-2-1-3-6-13)22-18-8-4-7-15-16(18)11-17-19(23-24-20(15)17)14-9-10-26-12-14/h1-10,12H,11H2,(H,22,25)(H,23,24) | 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 | 100 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of KDR by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50209153
(CHEMBL247389 | furan-2-carboxylic acid (3-thiophen...)Show SMILES O=C(Nc1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1)c1ccco1 Show InChI InChI=1S/C19H13N3O2S/c23-19(16-5-2-7-24-16)20-15-4-1-3-12-13(15)9-14-17(21-22-18(12)14)11-6-8-25-10-11/h1-8,10H,9H2,(H,20,23)(H,21,22) | 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 | 110 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of KDR by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Macrophage colony-stimulating factor 1 receptor
(Homo sapiens (Human)) | BDBM50209150
(2-methoxy-N-{3-[5-(3-phenoxy-prop-1-ynyl)-thiophen...)Show SMILES COCC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C26H21N3O3S/c1-31-15-24(30)27-23-11-5-10-20-21(23)14-22-25(28-29-26(20)22)17-13-19(33-16-17)9-6-12-32-18-7-3-2-4-8-18/h2-5,7-8,10-11,13,16H,12,14-15H2,1H3,(H,27,30)(H,28,29) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 113 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of CSF1R by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50209148
(CHEMBL246166 | N-{3-[5-(3-phenoxy-prop-1-ynyl)-thi...)Show SMILES COC(=O)C(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C26H19N3O4S/c1-32-26(31)25(30)27-22-11-5-10-19-20(22)14-21-23(28-29-24(19)21)16-13-18(34-15-16)9-6-12-33-17-7-3-2-4-8-17/h2-5,7-8,10-11,13,15H,12,14H2,1H3,(H,27,30)(H,28,29) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 127 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50209144
(2-(2-methoxy-ethoxy)-N-{3-[5-(3-phenoxy-prop-1-yny...)Show SMILES COCCOCC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C28H25N3O4S/c1-33-13-14-34-17-26(32)29-25-11-5-10-22-23(25)16-24-27(30-31-28(22)24)19-15-21(36-18-19)9-6-12-35-20-7-3-2-4-8-20/h2-5,7-8,10-11,15,18H,12-14,16-17H2,1H3,(H,29,32)(H,30,31) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 136 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt1 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50209150
(2-methoxy-N-{3-[5-(3-phenoxy-prop-1-ynyl)-thiophen...)Show SMILES COCC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C26H21N3O3S/c1-31-15-24(30)27-23-11-5-10-20-21(23)14-22-25(28-29-26(20)22)17-13-19(33-16-17)9-6-12-32-18-7-3-2-4-8-18/h2-5,7-8,10-11,13,16H,12,14-15H2,1H3,(H,27,30)(H,28,29) | 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 | 153 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt3 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50209156
(CHEMBL395427 | N-{3-[5-(3-phenoxy-prop-1-ynyl)-thi...)Show SMILES CCOC(=O)CC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C28H23N3O4S/c1-2-34-26(33)16-25(32)29-24-12-6-11-21-22(24)15-23-27(30-31-28(21)23)18-14-20(36-17-18)10-7-13-35-19-8-4-3-5-9-19/h3-6,8-9,11-12,14,17H,2,13,15-16H2,1H3,(H,29,32)(H,30,31) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 153 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt1 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50209150
(2-methoxy-N-{3-[5-(3-phenoxy-prop-1-ynyl)-thiophen...)Show SMILES COCC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C26H21N3O3S/c1-31-15-24(30)27-23-11-5-10-20-21(23)14-22-25(28-29-26(20)22)17-13-19(33-16-17)9-6-12-32-18-7-3-2-4-8-18/h2-5,7-8,10-11,13,16H,12,14-15H2,1H3,(H,27,30)(H,28,29) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 175 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50209146
(CHEMBL247585 | N-(3-thiophen-3-yl-2,4-dihydro-inde...)Show SMILES O=C(Nc1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1)c1ccccc1 Show InChI InChI=1S/C21H15N3OS/c25-21(13-5-2-1-3-6-13)22-18-8-4-7-15-16(18)11-17-19(23-24-20(15)17)14-9-10-26-12-14/h1-10,12H,11H2,(H,22,25)(H,23,24) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 180 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Macrophage colony-stimulating factor 1 receptor
(Homo sapiens (Human)) | BDBM50209148
(CHEMBL246166 | N-{3-[5-(3-phenoxy-prop-1-ynyl)-thi...)Show SMILES COC(=O)C(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C26H19N3O4S/c1-32-26(31)25(30)27-22-11-5-10-19-20(22)14-21-23(28-29-24(19)21)16-13-18(34-15-16)9-6-12-33-17-7-3-2-4-8-17/h2-5,7-8,10-11,13,15H,12,14H2,1H3,(H,27,30)(H,28,29) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 190 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of CSF1R by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50209159
(CHEMBL246343 | [(3-thiophen-3-yl-2,4-dihydro-inden...)Show SMILES OC(=O)CNC(=O)c1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1 Show InChI InChI=1S/C17H13N3O3S/c21-14(22)7-18-17(23)11-3-1-2-10-12(11)6-13-15(19-20-16(10)13)9-4-5-24-8-9/h1-5,8H,6-7H2,(H,18,23)(H,19,20)(H,21,22) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 240 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt1 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50209156
(CHEMBL395427 | N-{3-[5-(3-phenoxy-prop-1-ynyl)-thi...)Show SMILES CCOC(=O)CC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C28H23N3O4S/c1-2-34-26(33)16-25(32)29-24-12-6-11-21-22(24)15-23-27(30-31-28(21)23)18-14-20(36-17-18)10-7-13-35-19-8-4-3-5-9-19/h3-6,8-9,11-12,14,17H,2,13,15-16H2,1H3,(H,29,32)(H,30,31) | 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 | 263 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of KDR by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50209144
(2-(2-methoxy-ethoxy)-N-{3-[5-(3-phenoxy-prop-1-yny...)Show SMILES COCCOCC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C28H25N3O4S/c1-33-13-14-34-17-26(32)29-25-11-5-10-22-23(25)16-24-27(30-31-28(22)24)19-15-21(36-18-19)9-6-12-35-20-7-3-2-4-8-20/h2-5,7-8,10-11,15,18H,12-14,16-17H2,1H3,(H,29,32)(H,30,31) | 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 | 270 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of KDR by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50209160
(2-[(3-thiophen-3-yl-2,4-dihydro-indeno[1,2-c]pyraz...)Show InChI InChI=1S/C17H17N3OS/c21-6-5-18-9-11-2-1-3-13-14(11)8-15-16(19-20-17(13)15)12-4-7-22-10-12/h1-4,7,10,18,21H,5-6,8-9H2,(H,19,20) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 270 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt1 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50209161
(CHEMBL395694 | ethanesulfonic acid (3-thiophen-3-y...)Show SMILES CCS(=O)(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1 Show InChI InChI=1S/C16H15N3O2S2/c1-2-23(20,21)19-14-5-3-4-11-12(14)8-13-15(17-18-16(11)13)10-6-7-22-9-10/h3-7,9,19H,2,8H2,1H3,(H,17,18) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 290 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt1 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50209145
(CHEMBL245362 | N-(3-thiophen-3-yl-2,4-dihydro-inde...)Show InChI InChI=1S/C18H17N3OS/c1-2-4-16(22)19-15-6-3-5-12-13(15)9-14-17(20-21-18(12)14)11-7-8-23-10-11/h3,5-8,10H,2,4,9H2,1H3,(H,19,22)(H,20,21) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 290 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt1 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50209161
(CHEMBL395694 | ethanesulfonic acid (3-thiophen-3-y...)Show SMILES CCS(=O)(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1 Show InChI InChI=1S/C16H15N3O2S2/c1-2-23(20,21)19-14-5-3-4-11-12(14)8-13-15(17-18-16(11)13)10-6-7-22-9-10/h3-7,9,19H,2,8H2,1H3,(H,17,18) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 310 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of KDR by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50209147
(3-[(3-thiophen-3-yl-2,4-dihydro-indeno[1,2-c]pyraz...)Show SMILES OC(=O)CCNC(=O)c1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1 Show InChI InChI=1S/C18H15N3O3S/c22-15(23)4-6-19-18(24)12-3-1-2-11-13(12)8-14-16(20-21-17(11)14)10-5-7-25-9-10/h1-3,5,7,9H,4,6,8H2,(H,19,24)(H,20,21)(H,22,23) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 370 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt1 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50209159
(CHEMBL246343 | [(3-thiophen-3-yl-2,4-dihydro-inden...)Show SMILES OC(=O)CNC(=O)c1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1 Show InChI InChI=1S/C17H13N3O3S/c21-14(22)7-18-17(23)11-3-1-2-10-12(11)6-13-15(19-20-16(10)13)9-4-5-24-8-9/h1-5,8H,6-7H2,(H,18,23)(H,19,20)(H,21,22) | 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 | 410 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of KDR by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50209160
(2-[(3-thiophen-3-yl-2,4-dihydro-indeno[1,2-c]pyraz...)Show InChI InChI=1S/C17H17N3OS/c21-6-5-18-9-11-2-1-3-13-14(11)8-15-16(19-20-17(13)15)12-4-7-22-10-12/h1-4,7,10,18,21H,5-6,8-9H2,(H,19,20) | 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 | 440 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of KDR by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50209157
((3-thiophen-3-yl-2,4-dihydro-indeno[1,2-c]pyrazol-...)Show InChI InChI=1S/C17H15N3O2S/c1-2-22-17(21)18-14-5-3-4-11-12(14)8-13-15(19-20-16(11)13)10-6-7-23-9-10/h3-7,9H,2,8H2,1H3,(H,18,21)(H,19,20) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 450 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt1 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50209145
(CHEMBL245362 | N-(3-thiophen-3-yl-2,4-dihydro-inde...)Show InChI InChI=1S/C18H17N3OS/c1-2-4-16(22)19-15-6-3-5-12-13(15)9-14-17(20-21-18(12)14)11-7-8-23-10-11/h3,5-8,10H,2,4,9H2,1H3,(H,19,22)(H,20,21) | 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 | 560 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of KDR by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50209147
(3-[(3-thiophen-3-yl-2,4-dihydro-indeno[1,2-c]pyraz...)Show SMILES OC(=O)CCNC(=O)c1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1 Show InChI InChI=1S/C18H15N3O3S/c22-15(23)4-6-19-18(24)12-3-1-2-11-13(12)8-14-16(20-21-17(11)14)10-5-7-25-9-10/h1-3,5,7,9H,4,6,8H2,(H,19,24)(H,20,21)(H,22,23) | 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 | 580 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of KDR by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50209156
(CHEMBL395427 | N-{3-[5-(3-phenoxy-prop-1-ynyl)-thi...)Show SMILES CCOC(=O)CC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C28H23N3O4S/c1-2-34-26(33)16-25(32)29-24-12-6-11-21-22(24)15-23-27(30-31-28(21)23)18-14-20(36-17-18)10-7-13-35-19-8-4-3-5-9-19/h3-6,8-9,11-12,14,17H,2,13,15-16H2,1H3,(H,29,32)(H,30,31) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 619 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50209144
(2-(2-methoxy-ethoxy)-N-{3-[5-(3-phenoxy-prop-1-yny...)Show SMILES COCCOCC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C28H25N3O4S/c1-33-13-14-34-17-26(32)29-25-11-5-10-22-23(25)16-24-27(30-31-28(22)24)19-15-21(36-18-19)9-6-12-35-20-7-3-2-4-8-20/h2-5,7-8,10-11,15,18H,12-14,16-17H2,1H3,(H,29,32)(H,30,31) | 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 | 624 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt3 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50209157
((3-thiophen-3-yl-2,4-dihydro-indeno[1,2-c]pyrazol-...)Show InChI InChI=1S/C17H15N3O2S/c1-2-22-17(21)18-14-5-3-4-11-12(14)8-13-15(19-20-16(11)13)10-6-7-23-9-10/h3-7,9H,2,8H2,1H3,(H,18,21)(H,19,20) | 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 | 650 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of KDR by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50209150
(2-methoxy-N-{3-[5-(3-phenoxy-prop-1-ynyl)-thiophen...)Show SMILES COCC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C26H21N3O3S/c1-31-15-24(30)27-23-11-5-10-20-21(23)14-22-25(28-29-26(20)22)17-13-19(33-16-17)9-6-12-32-18-7-3-2-4-8-18/h2-5,7-8,10-11,13,16H,12,14-15H2,1H3,(H,27,30)(H,28,29) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 710 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt1 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50209162
(2-(4-methyl-piperazin-1-yl)-N-(3-thiophen-3-yl-2,4...)Show SMILES CN1CCN(CC(=O)Nc2cccc-3c2Cc2c-3n[nH]c2-c2ccsc2)CC1 Show InChI InChI=1S/C21H23N5OS/c1-25-6-8-26(9-7-25)12-19(27)22-18-4-2-3-15-16(18)11-17-20(23-24-21(15)17)14-5-10-28-13-14/h2-5,10,13H,6-9,11-12H2,1H3,(H,22,27)(H,23,24) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 710 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt1 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50209154
(5-methyl-isoxazole-3-carboxylic acid (3-thiophen-3...)Show SMILES Cc1cc(no1)C(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1 Show InChI InChI=1S/C19H14N4O2S/c1-10-7-16(23-25-10)19(24)20-15-4-2-3-12-13(15)8-14-17(21-22-18(12)14)11-5-6-26-9-11/h2-7,9H,8H2,1H3,(H,20,24)(H,21,22) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 900 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50209162
(2-(4-methyl-piperazin-1-yl)-N-(3-thiophen-3-yl-2,4...)Show SMILES CN1CCN(CC(=O)Nc2cccc-3c2Cc2c-3n[nH]c2-c2ccsc2)CC1 Show InChI InChI=1S/C21H23N5OS/c1-25-6-8-26(9-7-25)12-19(27)22-18-4-2-3-15-16(18)11-17-20(23-24-21(15)17)14-5-10-28-13-14/h2-5,10,13H,6-9,11-12H2,1H3,(H,22,27)(H,23,24) | 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 | 920 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of KDR by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50209153
(CHEMBL247389 | furan-2-carboxylic acid (3-thiophen...)Show SMILES O=C(Nc1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1)c1ccco1 Show InChI InChI=1S/C19H13N3O2S/c23-19(16-5-2-7-24-16)20-15-4-1-3-12-13(15)9-14-17(21-22-18(12)14)11-6-8-25-10-11/h1-8,10H,9H2,(H,20,23)(H,21,22) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50209156
(CHEMBL395427 | N-{3-[5-(3-phenoxy-prop-1-ynyl)-thi...)Show SMILES CCOC(=O)CC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C28H23N3O4S/c1-2-34-26(33)16-25(32)29-24-12-6-11-21-22(24)15-23-27(30-31-28(21)23)18-14-20(36-17-18)10-7-13-35-19-8-4-3-5-9-19/h3-6,8-9,11-12,14,17H,2,13,15-16H2,1H3,(H,29,32)(H,30,31) | 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 | 1.11E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt3 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50209151
(CHEMBL247388 | N-(3-thiophen-3-yl-2,4-dihydro-inde...)Show SMILES COC(=O)C(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1 Show InChI InChI=1S/C17H13N3O3S/c1-23-17(22)16(21)18-13-4-2-3-10-11(13)7-12-14(19-20-15(10)12)9-5-6-24-8-9/h2-6,8H,7H2,1H3,(H,18,21)(H,19,20) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.12E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Macrophage colony-stimulating factor 1 receptor
(Homo sapiens (Human)) | BDBM50209144
(2-(2-methoxy-ethoxy)-N-{3-[5-(3-phenoxy-prop-1-yny...)Show SMILES COCCOCC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C28H25N3O4S/c1-33-13-14-34-17-26(32)29-25-11-5-10-22-23(25)16-24-27(30-31-28(22)24)19-15-21(36-18-19)9-6-12-35-20-7-3-2-4-8-20/h2-5,7-8,10-11,15,18H,12-14,16-17H2,1H3,(H,29,32)(H,30,31) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.27E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of CSF1R by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50209143
(2-methoxy-N-(3-thiophen-3-yl-2,4-dihydro-indeno[1,...)Show InChI InChI=1S/C17H15N3O2S/c1-22-8-15(21)18-14-4-2-3-11-12(14)7-13-16(19-20-17(11)13)10-5-6-23-9-10/h2-6,9H,7-8H2,1H3,(H,18,21)(H,19,20) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.58E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50209160
(2-[(3-thiophen-3-yl-2,4-dihydro-indeno[1,2-c]pyraz...)Show InChI InChI=1S/C17H17N3OS/c21-6-5-18-9-11-2-1-3-13-14(11)8-15-16(19-20-17(13)15)12-4-7-22-10-12/h1-4,7,10,18,21H,5-6,8-9H2,(H,19,20) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.67E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50209157
((3-thiophen-3-yl-2,4-dihydro-indeno[1,2-c]pyrazol-...)Show InChI InChI=1S/C17H15N3O2S/c1-2-22-17(21)18-14-5-3-4-11-12(14)8-13-15(19-20-16(11)13)10-6-7-23-9-10/h3-7,9H,2,8H2,1H3,(H,18,21)(H,19,20) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.55E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Macrophage colony-stimulating factor 1 receptor
(Homo sapiens (Human)) | BDBM50209156
(CHEMBL395427 | N-{3-[5-(3-phenoxy-prop-1-ynyl)-thi...)Show SMILES CCOC(=O)CC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C28H23N3O4S/c1-2-34-26(33)16-25(32)29-24-12-6-11-21-22(24)15-23-27(30-31-28(21)23)18-14-20(36-17-18)10-7-13-35-19-8-4-3-5-9-19/h3-6,8-9,11-12,14,17H,2,13,15-16H2,1H3,(H,29,32)(H,30,31) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.98E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of CSF1R by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50209149
(1-(3-thiophen-3-yl-2,4-dihydro-indeno[1,2-c]pyrazo...)Show SMILES OC(=O)C1CCCN(C1)C(=O)c1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1 Show InChI InChI=1S/C21H19N3O3S/c25-20(24-7-2-3-12(10-24)21(26)27)15-5-1-4-14-16(15)9-17-18(22-23-19(14)17)13-6-8-28-11-13/h1,4-6,8,11-12H,2-3,7,9-10H2,(H,22,23)(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 | 3.08E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt1 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50209155
(1-(3-thiophen-3-yl-2,4-dihydro-indeno[1,2-c]pyrazo...)Show SMILES OC(=O)C1CCN(CC1)C(=O)c1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1 Show InChI InChI=1S/C21H19N3O3S/c25-20(24-7-4-12(5-8-24)21(26)27)15-3-1-2-14-16(15)10-17-18(22-23-19(14)17)13-6-9-28-11-13/h1-3,6,9,11-12H,4-5,7-8,10H2,(H,22,23)(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 | 3.47E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt1 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50209144
(2-(2-methoxy-ethoxy)-N-{3-[5-(3-phenoxy-prop-1-yny...)Show SMILES COCCOCC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C28H25N3O4S/c1-33-13-14-34-17-26(32)29-25-11-5-10-22-23(25)16-24-27(30-31-28(22)24)19-15-21(36-18-19)9-6-12-35-20-7-3-2-4-8-20/h2-5,7-8,10-11,15,18H,12-14,16-17H2,1H3,(H,29,32)(H,30,31) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 4.33E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50209162
(2-(4-methyl-piperazin-1-yl)-N-(3-thiophen-3-yl-2,4...)Show SMILES CN1CCN(CC(=O)Nc2cccc-3c2Cc2c-3n[nH]c2-c2ccsc2)CC1 Show InChI InChI=1S/C21H23N5OS/c1-25-6-8-26(9-7-25)12-19(27)22-18-4-2-3-15-16(18)11-17-20(23-24-21(15)17)14-5-10-28-13-14/h2-5,10,13H,6-9,11-12H2,1H3,(H,22,27)(H,23,24) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 4.33E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50209161
(CHEMBL395694 | ethanesulfonic acid (3-thiophen-3-y...)Show SMILES CCS(=O)(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1 Show InChI InChI=1S/C16H15N3O2S2/c1-2-23(20,21)19-14-5-3-4-11-12(14)8-13-15(17-18-16(11)13)10-6-7-22-9-10/h3-7,9,19H,2,8H2,1H3,(H,17,18) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 4.39E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50209149
(1-(3-thiophen-3-yl-2,4-dihydro-indeno[1,2-c]pyrazo...)Show SMILES OC(=O)C1CCCN(C1)C(=O)c1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1 Show InChI InChI=1S/C21H19N3O3S/c25-20(24-7-2-3-12(10-24)21(26)27)15-5-1-4-14-16(15)9-17-18(22-23-19(14)17)13-6-8-28-11-13/h1,4-6,8,11-12H,2-3,7,9-10H2,(H,22,23)(H,26,27) | 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 | 4.84E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of KDR by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Angiopoietin-1 receptor
(Homo sapiens (Human)) | BDBM50209158
(2-(4-methyl-piperazin-1-yl)-N-{3-[5-(3-phenoxy-pro...)Show SMILES CN1CCN(CC(=O)Nc2cccc-3c2Cc2c-3n[nH]c2-c2csc(c2)C#CCOc2ccccc2)CC1 Show InChI InChI=1S/C30H29N5O2S/c1-34-12-14-35(15-13-34)19-28(36)31-27-11-5-10-24-25(27)18-26-29(32-33-30(24)26)21-17-23(38-20-21)9-6-16-37-22-7-3-2-4-8-22/h2-5,7-8,10-11,17,20H,12-16,18-19H2,1H3,(H,31,36)(H,32,33) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 4.88E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Tie2 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50209159
(CHEMBL246343 | [(3-thiophen-3-yl-2,4-dihydro-inden...)Show SMILES OC(=O)CNC(=O)c1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1 Show InChI InChI=1S/C17H13N3O3S/c21-14(22)7-18-17(23)11-3-1-2-10-12(11)6-13-15(19-20-16(10)13)9-4-5-24-8-9/h1-5,8H,6-7H2,(H,18,23)(H,19,20)(H,21,22) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 5.15E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50209147
(3-[(3-thiophen-3-yl-2,4-dihydro-indeno[1,2-c]pyraz...)Show SMILES OC(=O)CCNC(=O)c1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1 Show InChI InChI=1S/C18H15N3O3S/c22-15(23)4-6-19-18(24)12-3-1-2-11-13(12)8-14-16(20-21-17(11)14)10-5-7-25-9-10/h1-3,5,7,9H,4,6,8H2,(H,19,24)(H,20,21)(H,22,23) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 5.61E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50209155
(1-(3-thiophen-3-yl-2,4-dihydro-indeno[1,2-c]pyrazo...)Show SMILES OC(=O)C1CCN(CC1)C(=O)c1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1 Show InChI InChI=1S/C21H19N3O3S/c25-20(24-7-4-12(5-8-24)21(26)27)15-3-1-2-14-16(15)10-17-18(22-23-19(14)17)13-6-9-28-11-13/h1-3,6,9,11-12H,4-5,7-8,10H2,(H,22,23)(H,26,27) | 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 | 7.04E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of KDR by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50209152
(CHEMBL245934 | [1-(3-thiophen-3-yl-2,4-dihydro-ind...)Show SMILES OCC1CCN(Cc2cccc-3c2Cc2c-3n[nH]c2-c2ccsc2)CC1 Show InChI InChI=1S/C21H23N3OS/c25-12-14-4-7-24(8-5-14)11-15-2-1-3-17-18(15)10-19-20(22-23-21(17)19)16-6-9-26-13-16/h1-3,6,9,13-14,25H,4-5,7-8,10-12H2,(H,22,23) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 7.18E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50209145
(CHEMBL245362 | N-(3-thiophen-3-yl-2,4-dihydro-inde...)Show InChI InChI=1S/C18H17N3OS/c1-2-4-16(22)19-15-6-3-5-12-13(15)9-14-17(20-21-18(12)14)11-7-8-23-10-11/h3,5-8,10H,2,4,9H2,1H3,(H,19,22)(H,20,21) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 9.54E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Angiopoietin-1 receptor
(Homo sapiens (Human)) | BDBM50209144
(2-(2-methoxy-ethoxy)-N-{3-[5-(3-phenoxy-prop-1-yny...)Show SMILES COCCOCC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C28H25N3O4S/c1-33-13-14-34-17-26(32)29-25-11-5-10-22-23(25)16-24-27(30-31-28(22)24)19-15-21(36-18-19)9-6-12-35-20-7-3-2-4-8-20/h2-5,7-8,10-11,15,18H,12-14,16-17H2,1H3,(H,29,32)(H,30,31) | 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+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Tie2 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Fyn
(Homo sapiens (Human)) | BDBM50209150
(2-methoxy-N-{3-[5-(3-phenoxy-prop-1-ynyl)-thiophen...)Show SMILES COCC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C26H21N3O3S/c1-31-15-24(30)27-23-11-5-10-20-21(23)14-22-25(28-29-26(20)22)17-13-19(33-16-17)9-6-12-32-18-7-3-2-4-8-18/h2-5,7-8,10-11,13,16H,12,14-15H2,1H3,(H,27,30)(H,28,29) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.37E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Fyn by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50209150
(2-methoxy-N-{3-[5-(3-phenoxy-prop-1-ynyl)-thiophen...)Show SMILES COCC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C26H21N3O3S/c1-31-15-24(30)27-23-11-5-10-20-21(23)14-22-25(28-29-26(20)22)17-13-19(33-16-17)9-6-12-32-18-7-3-2-4-8-18/h2-5,7-8,10-11,13,16H,12,14-15H2,1H3,(H,27,30)(H,28,29) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Lck by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50209152
(CHEMBL245934 | [1-(3-thiophen-3-yl-2,4-dihydro-ind...)Show SMILES OCC1CCN(Cc2cccc-3c2Cc2c-3n[nH]c2-c2ccsc2)CC1 Show InChI InChI=1S/C21H23N3OS/c25-12-14-4-7-24(8-5-14)11-15-2-1-3-17-18(15)10-19-20(22-23-21(17)19)16-6-9-26-13-16/h1-3,6,9,13-14,25H,4-5,7-8,10-12H2,(H,22,23) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.76E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Flt1 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Lyn
(Homo sapiens (Human)) | BDBM50209150
(2-methoxy-N-{3-[5-(3-phenoxy-prop-1-ynyl)-thiophen...)Show SMILES COCC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C26H21N3O3S/c1-31-15-24(30)27-23-11-5-10-20-21(23)14-22-25(28-29-26(20)22)17-13-19(33-16-17)9-6-12-32-18-7-3-2-4-8-18/h2-5,7-8,10-11,13,16H,12,14-15H2,1H3,(H,27,30)(H,28,29) | 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 | 2.08E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Lyn by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50209148
(CHEMBL246166 | N-{3-[5-(3-phenoxy-prop-1-ynyl)-thi...)Show SMILES COC(=O)C(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C26H19N3O4S/c1-32-26(31)25(30)27-22-11-5-10-19-20(22)14-21-23(28-29-24(19)21)16-13-18(34-15-16)9-6-12-33-17-7-3-2-4-8-17/h2-5,7-8,10-11,13,15H,12,14H2,1H3,(H,27,30)(H,28,29) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.14E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Lck by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Fyn
(Homo sapiens (Human)) | BDBM50209148
(CHEMBL246166 | N-{3-[5-(3-phenoxy-prop-1-ynyl)-thi...)Show SMILES COC(=O)C(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C26H19N3O4S/c1-32-26(31)25(30)27-22-11-5-10-19-20(22)14-21-23(28-29-24(19)21)16-13-18(34-15-16)9-6-12-33-17-7-3-2-4-8-17/h2-5,7-8,10-11,13,15H,12,14H2,1H3,(H,27,30)(H,28,29) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.30E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Fyn by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Angiopoietin-1 receptor
(Homo sapiens (Human)) | BDBM50209148
(CHEMBL246166 | N-{3-[5-(3-phenoxy-prop-1-ynyl)-thi...)Show SMILES COC(=O)C(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C26H19N3O4S/c1-32-26(31)25(30)27-22-11-5-10-19-20(22)14-21-23(28-29-24(19)21)16-13-18(34-15-16)9-6-12-33-17-7-3-2-4-8-17/h2-5,7-8,10-11,13,15H,12,14H2,1H3,(H,27,30)(H,28,29) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.47E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Tie2 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50209156
(CHEMBL395427 | N-{3-[5-(3-phenoxy-prop-1-ynyl)-thi...)Show SMILES CCOC(=O)CC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C28H23N3O4S/c1-2-34-26(33)16-25(32)29-24-12-6-11-21-22(24)15-23-27(30-31-28(21)23)18-14-20(36-17-18)10-7-13-35-19-8-4-3-5-9-19/h3-6,8-9,11-12,14,17H,2,13,15-16H2,1H3,(H,29,32)(H,30,31) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.65E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Lck by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50209152
(CHEMBL245934 | [1-(3-thiophen-3-yl-2,4-dihydro-ind...)Show SMILES OCC1CCN(Cc2cccc-3c2Cc2c-3n[nH]c2-c2ccsc2)CC1 Show InChI InChI=1S/C21H23N3OS/c25-12-14-4-7-24(8-5-14)11-15-2-1-3-17-18(15)10-19-20(22-23-21(17)19)16-6-9-26-13-16/h1-3,6,9,13-14,25H,4-5,7-8,10-12H2,(H,22,23) | 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 | 2.79E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of KDR by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase HCK
(Homo sapiens (Human)) | BDBM50209150
(2-methoxy-N-{3-[5-(3-phenoxy-prop-1-ynyl)-thiophen...)Show SMILES COCC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C26H21N3O3S/c1-31-15-24(30)27-23-11-5-10-20-21(23)14-22-25(28-29-26(20)22)17-13-19(33-16-17)9-6-12-32-18-7-3-2-4-8-18/h2-5,7-8,10-11,13,16H,12,14-15H2,1H3,(H,27,30)(H,28,29) | 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 | 3.03E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Hck by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Lyn
(Homo sapiens (Human)) | BDBM50209148
(CHEMBL246166 | N-{3-[5-(3-phenoxy-prop-1-ynyl)-thi...)Show SMILES COC(=O)C(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C26H19N3O4S/c1-32-26(31)25(30)27-22-11-5-10-19-20(22)14-21-23(28-29-24(19)21)16-13-18(34-15-16)9-6-12-33-17-7-3-2-4-8-17/h2-5,7-8,10-11,13,15H,12,14H2,1H3,(H,27,30)(H,28,29) | 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 | 3.06E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Lyn by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50209158
(2-(4-methyl-piperazin-1-yl)-N-{3-[5-(3-phenoxy-pro...)Show SMILES CN1CCN(CC(=O)Nc2cccc-3c2Cc2c-3n[nH]c2-c2csc(c2)C#CCOc2ccccc2)CC1 Show InChI InChI=1S/C30H29N5O2S/c1-34-12-14-35(15-13-34)19-28(36)31-27-11-5-10-24-25(27)18-26-29(32-33-30(24)26)21-17-23(38-20-21)9-6-16-37-22-7-3-2-4-8-22/h2-5,7-8,10-11,17,20H,12-16,18-19H2,1H3,(H,31,36)(H,32,33) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 3.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Lck by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Angiopoietin-1 receptor
(Homo sapiens (Human)) | BDBM50209150
(2-methoxy-N-{3-[5-(3-phenoxy-prop-1-ynyl)-thiophen...)Show SMILES COCC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C26H21N3O3S/c1-31-15-24(30)27-23-11-5-10-20-21(23)14-22-25(28-29-26(20)22)17-13-19(33-16-17)9-6-12-32-18-7-3-2-4-8-18/h2-5,7-8,10-11,13,16H,12,14-15H2,1H3,(H,27,30)(H,28,29) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 4.06E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Tie2 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50209150
(2-methoxy-N-{3-[5-(3-phenoxy-prop-1-ynyl)-thiophen...)Show SMILES COCC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C26H21N3O3S/c1-31-15-24(30)27-23-11-5-10-20-21(23)14-22-25(28-29-26(20)22)17-13-19(33-16-17)9-6-12-32-18-7-3-2-4-8-18/h2-5,7-8,10-11,13,16H,12,14-15H2,1H3,(H,27,30)(H,28,29) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 4.33E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Src by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Lyn
(Homo sapiens (Human)) | BDBM50209156
(CHEMBL395427 | N-{3-[5-(3-phenoxy-prop-1-ynyl)-thi...)Show SMILES CCOC(=O)CC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C28H23N3O4S/c1-2-34-26(33)16-25(32)29-24-12-6-11-21-22(24)15-23-27(30-31-28(21)23)18-14-20(36-17-18)10-7-13-35-19-8-4-3-5-9-19/h3-6,8-9,11-12,14,17H,2,13,15-16H2,1H3,(H,29,32)(H,30,31) | 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 | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Lyn by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50209149
(1-(3-thiophen-3-yl-2,4-dihydro-indeno[1,2-c]pyrazo...)Show SMILES OC(=O)C1CCCN(C1)C(=O)c1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1 Show InChI InChI=1S/C21H19N3O3S/c25-20(24-7-2-3-12(10-24)21(26)27)15-5-1-4-14-16(15)9-17-18(22-23-19(14)17)13-6-8-28-11-13/h1,4-6,8,11-12H,2-3,7,9-10H2,(H,22,23)(H,26,27) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50209148
(CHEMBL246166 | N-{3-[5-(3-phenoxy-prop-1-ynyl)-thi...)Show SMILES COC(=O)C(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C26H19N3O4S/c1-32-26(31)25(30)27-22-11-5-10-19-20(22)14-21-23(28-29-24(19)21)16-13-18(34-15-16)9-6-12-33-17-7-3-2-4-8-17/h2-5,7-8,10-11,13,15H,12,14H2,1H3,(H,27,30)(H,28,29) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Src by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase HCK
(Homo sapiens (Human)) | BDBM50209158
(2-(4-methyl-piperazin-1-yl)-N-{3-[5-(3-phenoxy-pro...)Show SMILES CN1CCN(CC(=O)Nc2cccc-3c2Cc2c-3n[nH]c2-c2csc(c2)C#CCOc2ccccc2)CC1 Show InChI InChI=1S/C30H29N5O2S/c1-34-12-14-35(15-13-34)19-28(36)31-27-11-5-10-24-25(27)18-26-29(32-33-30(24)26)21-17-23(38-20-21)9-6-16-37-22-7-3-2-4-8-22/h2-5,7-8,10-11,17,20H,12-16,18-19H2,1H3,(H,31,36)(H,32,33) | 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 | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Hck by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Lyn
(Homo sapiens (Human)) | BDBM50209144
(2-(2-methoxy-ethoxy)-N-{3-[5-(3-phenoxy-prop-1-yny...)Show SMILES COCCOCC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C28H25N3O4S/c1-33-13-14-34-17-26(32)29-25-11-5-10-22-23(25)16-24-27(30-31-28(22)24)19-15-21(36-18-19)9-6-12-35-20-7-3-2-4-8-20/h2-5,7-8,10-11,15,18H,12-14,16-17H2,1H3,(H,29,32)(H,30,31) | 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 | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Lyn by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50209155
(1-(3-thiophen-3-yl-2,4-dihydro-indeno[1,2-c]pyrazo...)Show SMILES OC(=O)C1CCN(CC1)C(=O)c1cccc-2c1Cc1c-2n[nH]c1-c1ccsc1 Show InChI InChI=1S/C21H19N3O3S/c25-20(24-7-4-12(5-8-24)21(26)27)15-3-1-2-14-16(15)10-17-18(22-23-19(14)17)13-6-9-28-11-13/h1-3,6,9,11-12H,4-5,7-8,10H2,(H,22,23)(H,26,27) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of c-Kit by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Lyn
(Homo sapiens (Human)) | BDBM50209158
(2-(4-methyl-piperazin-1-yl)-N-{3-[5-(3-phenoxy-pro...)Show SMILES CN1CCN(CC(=O)Nc2cccc-3c2Cc2c-3n[nH]c2-c2csc(c2)C#CCOc2ccccc2)CC1 Show InChI InChI=1S/C30H29N5O2S/c1-34-12-14-35(15-13-34)19-28(36)31-27-11-5-10-24-25(27)18-26-29(32-33-30(24)26)21-17-23(38-20-21)9-6-16-37-22-7-3-2-4-8-22/h2-5,7-8,10-11,17,20H,12-16,18-19H2,1H3,(H,31,36)(H,32,33) | 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 | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Lyn by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase HCK
(Homo sapiens (Human)) | BDBM50209144
(2-(2-methoxy-ethoxy)-N-{3-[5-(3-phenoxy-prop-1-yny...)Show SMILES COCCOCC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C28H25N3O4S/c1-33-13-14-34-17-26(32)29-25-11-5-10-22-23(25)16-24-27(30-31-28(22)24)19-15-21(36-18-19)9-6-12-35-20-7-3-2-4-8-20/h2-5,7-8,10-11,15,18H,12-14,16-17H2,1H3,(H,29,32)(H,30,31) | 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 | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Hck by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50209158
(2-(4-methyl-piperazin-1-yl)-N-{3-[5-(3-phenoxy-pro...)Show SMILES CN1CCN(CC(=O)Nc2cccc-3c2Cc2c-3n[nH]c2-c2csc(c2)C#CCOc2ccccc2)CC1 Show InChI InChI=1S/C30H29N5O2S/c1-34-12-14-35(15-13-34)19-28(36)31-27-11-5-10-24-25(27)18-26-29(32-33-30(24)26)21-17-23(38-20-21)9-6-16-37-22-7-3-2-4-8-22/h2-5,7-8,10-11,17,20H,12-16,18-19H2,1H3,(H,31,36)(H,32,33) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Src by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Angiopoietin-1 receptor
(Homo sapiens (Human)) | BDBM50209156
(CHEMBL395427 | N-{3-[5-(3-phenoxy-prop-1-ynyl)-thi...)Show SMILES CCOC(=O)CC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C28H23N3O4S/c1-2-34-26(33)16-25(32)29-24-12-6-11-21-22(24)15-23-27(30-31-28(21)23)18-14-20(36-17-18)10-7-13-35-19-8-4-3-5-9-19/h3-6,8-9,11-12,14,17H,2,13,15-16H2,1H3,(H,29,32)(H,30,31) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Tie2 by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Fyn
(Homo sapiens (Human)) | BDBM50209144
(2-(2-methoxy-ethoxy)-N-{3-[5-(3-phenoxy-prop-1-yny...)Show SMILES COCCOCC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C28H25N3O4S/c1-33-13-14-34-17-26(32)29-25-11-5-10-22-23(25)16-24-27(30-31-28(22)24)19-15-21(36-18-19)9-6-12-35-20-7-3-2-4-8-20/h2-5,7-8,10-11,15,18H,12-14,16-17H2,1H3,(H,29,32)(H,30,31) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Fyn by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50209156
(CHEMBL395427 | N-{3-[5-(3-phenoxy-prop-1-ynyl)-thi...)Show SMILES CCOC(=O)CC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C28H23N3O4S/c1-2-34-26(33)16-25(32)29-24-12-6-11-21-22(24)15-23-27(30-31-28(21)23)18-14-20(36-17-18)10-7-13-35-19-8-4-3-5-9-19/h3-6,8-9,11-12,14,17H,2,13,15-16H2,1H3,(H,29,32)(H,30,31) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Src by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50209144
(2-(2-methoxy-ethoxy)-N-{3-[5-(3-phenoxy-prop-1-yny...)Show SMILES COCCOCC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C28H25N3O4S/c1-33-13-14-34-17-26(32)29-25-11-5-10-22-23(25)16-24-27(30-31-28(22)24)19-15-21(36-18-19)9-6-12-35-20-7-3-2-4-8-20/h2-5,7-8,10-11,15,18H,12-14,16-17H2,1H3,(H,29,32)(H,30,31) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Lck by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Fyn
(Homo sapiens (Human)) | BDBM50209158
(2-(4-methyl-piperazin-1-yl)-N-{3-[5-(3-phenoxy-pro...)Show SMILES CN1CCN(CC(=O)Nc2cccc-3c2Cc2c-3n[nH]c2-c2csc(c2)C#CCOc2ccccc2)CC1 Show InChI InChI=1S/C30H29N5O2S/c1-34-12-14-35(15-13-34)19-28(36)31-27-11-5-10-24-25(27)18-26-29(32-33-30(24)26)21-17-23(38-20-21)9-6-16-37-22-7-3-2-4-8-22/h2-5,7-8,10-11,17,20H,12-16,18-19H2,1H3,(H,31,36)(H,32,33) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Fyn by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase HCK
(Homo sapiens (Human)) | BDBM50209156
(CHEMBL395427 | N-{3-[5-(3-phenoxy-prop-1-ynyl)-thi...)Show SMILES CCOC(=O)CC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C28H23N3O4S/c1-2-34-26(33)16-25(32)29-24-12-6-11-21-22(24)15-23-27(30-31-28(21)23)18-14-20(36-17-18)10-7-13-35-19-8-4-3-5-9-19/h3-6,8-9,11-12,14,17H,2,13,15-16H2,1H3,(H,29,32)(H,30,31) | 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 | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Hck by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Fyn
(Homo sapiens (Human)) | BDBM50209156
(CHEMBL395427 | N-{3-[5-(3-phenoxy-prop-1-ynyl)-thi...)Show SMILES CCOC(=O)CC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C28H23N3O4S/c1-2-34-26(33)16-25(32)29-24-12-6-11-21-22(24)15-23-27(30-31-28(21)23)18-14-20(36-17-18)10-7-13-35-19-8-4-3-5-9-19/h3-6,8-9,11-12,14,17H,2,13,15-16H2,1H3,(H,29,32)(H,30,31) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Fyn by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase HCK
(Homo sapiens (Human)) | BDBM50209148
(CHEMBL246166 | N-{3-[5-(3-phenoxy-prop-1-ynyl)-thi...)Show SMILES COC(=O)C(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C26H19N3O4S/c1-32-26(31)25(30)27-22-11-5-10-19-20(22)14-21-23(28-29-24(19)21)16-13-18(34-15-16)9-6-12-33-17-7-3-2-4-8-17/h2-5,7-8,10-11,13,15H,12,14H2,1H3,(H,27,30)(H,28,29) | 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 | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Hck by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50209144
(2-(2-methoxy-ethoxy)-N-{3-[5-(3-phenoxy-prop-1-yny...)Show SMILES COCCOCC(=O)Nc1cccc-2c1Cc1c-2n[nH]c1-c1csc(c1)C#CCOc1ccccc1 Show InChI InChI=1S/C28H25N3O4S/c1-33-13-14-34-17-26(32)29-25-11-5-10-22-23(25)16-24-27(30-31-28(22)24)19-15-21(36-18-19)9-6-12-35-20-7-3-2-4-8-20/h2-5,7-8,10-11,15,18H,12-14,16-17H2,1H3,(H,29,32)(H,30,31) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description
Inhibition of Src by HTRF assay |
Bioorg Med Chem Lett 17: 3136-40 (2007)
Article DOI: 10.1016/j.bmcl.2007.03.031
BindingDB Entry DOI: 10.7270/Q2VD6Z3Q |
More data for this
Ligand-Target Pair | |
Search and Browse
