Found 203 hits with Last Name = 'tokuyama' and Initial = 'r' 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)) | BDBM50188272
(7-((1H-imidazol-1-yl)methyl)-3-(thiophen-3-yl)-1,4...)Show InChI InChI=1S/C18H14N4S/c1-2-13-8-16-17(14-3-6-23-10-14)20-21-18(16)15(13)7-12(1)9-22-5-4-19-11-22/h1-7,10-11H,8-9H2,(H,20,21) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 103 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of cKit by HTRF assay |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50188266
(7-((4-methylpiperazin-1-yl)methyl)-3-(thiophen-3-y...)Show SMILES CN1CCN(Cc2ccc3Cc4c(n[nH]c4-c4ccsc4)-c3c2)CC1 Show InChI InChI=1S/C20H22N4S/c1-23-5-7-24(8-6-23)12-14-2-3-15-11-18-19(16-4-9-25-13-16)21-22-20(18)17(15)10-14/h2-4,9-10,13H,5-8,11-12H2,1H3,(H,21,22) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 145 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of cKit by HTRF assay |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 3
(Homo sapiens (Human)) | BDBM50188272
(7-((1H-imidazol-1-yl)methyl)-3-(thiophen-3-yl)-1,4...)Show InChI InChI=1S/C18H14N4S/c1-2-13-8-16-17(14-3-6-23-10-14)20-21-18(16)15(13)7-12(1)9-22-5-4-19-11-22/h1-7,10-11H,8-9H2,(H,20,21) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 169 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of FLT4 by HTRF assay |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188266
(7-((4-methylpiperazin-1-yl)methyl)-3-(thiophen-3-y...)Show SMILES CN1CCN(Cc2ccc3Cc4c(n[nH]c4-c4ccsc4)-c3c2)CC1 Show InChI InChI=1S/C20H22N4S/c1-23-5-7-24(8-6-23)12-14-2-3-15-11-18-19(16-4-9-25-13-16)21-22-20(18)17(15)10-14/h2-4,9-10,13H,5-8,11-12H2,1H3,(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 | 180 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188272
(7-((1H-imidazol-1-yl)methyl)-3-(thiophen-3-yl)-1,4...)Show InChI InChI=1S/C18H14N4S/c1-2-13-8-16-17(14-3-6-23-10-14)20-21-18(16)15(13)7-12(1)9-22-5-4-19-11-22/h1-7,10-11H,8-9H2,(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 | 293 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188283
(6-((4-methylpiperazin-1-yl)methyl)-3-(thiophen-3-y...)Show SMILES CN1CCN(Cc2ccc-3c(Cc4c-3n[nH]c4-c3ccsc3)c2)CC1 Show InChI InChI=1S/C20H22N4S/c1-23-5-7-24(8-6-23)12-14-2-3-17-16(10-14)11-18-19(21-22-20(17)18)15-4-9-25-13-15/h2-4,9-10,13H,5-8,11-12H2,1H3,(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 | 400 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188281
(4-(6-((4-methylpiperazin-1-yl)methyl)-1,4-dihydroi...)Show SMILES CN1CCN(Cc2ccc-3c(Cc4c(n[nH]c-34)-c3ccc(O)cc3)c2)CC1 Show InChI InChI=1S/C22H24N4O/c1-25-8-10-26(11-9-25)14-15-2-7-19-17(12-15)13-20-21(23-24-22(19)20)16-3-5-18(27)6-4-16/h2-7,12,27H,8-11,13-14H2,1H3,(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 | 500 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188290
(7-((4-methylpiperazin-1-yl)methyl)-3-phenyl-1,4-di...)Show SMILES CN1CCN(Cc2ccc3Cc4c([nH]nc4-c4ccccc4)-c3c2)CC1 Show InChI InChI=1S/C22H24N4/c1-25-9-11-26(12-10-25)15-16-7-8-18-14-20-21(17-5-3-2-4-6-17)23-24-22(20)19(18)13-16/h2-8,13H,9-12,14-15H2,1H3,(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 | 600 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50188272
(7-((1H-imidazol-1-yl)methyl)-3-(thiophen-3-yl)-1,4...)Show InChI InChI=1S/C18H14N4S/c1-2-13-8-16-17(14-3-6-23-10-14)20-21-18(16)15(13)7-12(1)9-22-5-4-19-11-22/h1-7,10-11H,8-9H2,(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 | 601 | 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 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188275
(6-((4-methylpiperazin-1-yl)methyl)-3-phenyl-1,4-di...)Show SMILES CN1CCN(Cc2ccc-3c(Cc4c-3[nH]nc4-c3ccccc3)c2)CC1 Show InChI InChI=1S/C22H24N4/c1-25-9-11-26(12-10-25)15-16-7-8-19-18(13-16)14-20-21(23-24-22(19)20)17-5-3-2-4-6-17/h2-8,13H,9-12,14-15H2,1H3,(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 | 700 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188292
(3-(thiophen-2-yl)-1,4-dihydroindeno[1,2-c]pyrazole...)Show InChI InChI=1S/C14H10N2S/c1-2-5-10-9(4-1)8-11-13(10)15-16-14(11)12-6-3-7-17-12/h1-7H,8H2,(H,15,16) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 930 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 1
(Homo sapiens (Human)) | BDBM50188266
(7-((4-methylpiperazin-1-yl)methyl)-3-(thiophen-3-y...)Show SMILES CN1CCN(Cc2ccc3Cc4c(n[nH]c4-c4ccsc4)-c3c2)CC1 Show InChI InChI=1S/C20H22N4S/c1-23-5-7-24(8-6-23)12-14-2-3-15-11-18-19(16-4-9-25-13-16)21-22-20(18)17(15)10-14/h2-4,9-10,13H,5-8,11-12H2,1H3,(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 | 970 | 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 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188271
(6-((4-methylpiperazin-1-yl)methyl)-3-(thiophen-2-y...)Show SMILES CN1CCN(Cc2ccc-3c(Cc4c-3n[nH]c4-c3cccs3)c2)CC1 Show InChI InChI=1S/C20H22N4S/c1-23-6-8-24(9-7-23)13-14-4-5-16-15(11-14)12-17-19(16)21-22-20(17)18-3-2-10-25-18/h2-5,10-11H,6-9,12-13H2,1H3,(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 | 1.05E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188284
(3-phenyl-1,4-dihydroindeno[1,2-c]pyrazole | CHEMBL...)Show InChI InChI=1S/C16H12N2/c1-2-6-11(7-3-1)15-14-10-12-8-4-5-9-13(12)16(14)18-17-15/h1-9H,10H2,(H,17,18) | 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 | 1.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188269
(3-(4-((4-methylpiperazin-1-yl)methyl)phenyl)-1,4-d...)Show SMILES CN1CCN(Cc2ccc(cc2)-c2[nH]nc-3c2Cc2ccccc-32)CC1 Show InChI InChI=1S/C22H24N4/c1-25-10-12-26(13-11-25)15-16-6-8-17(9-7-16)21-20-14-18-4-2-3-5-19(18)22(20)24-23-21/h2-9H,10-15H2,1H3,(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 | 1.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 3
(Homo sapiens (Human)) | BDBM50188266
(7-((4-methylpiperazin-1-yl)methyl)-3-(thiophen-3-y...)Show SMILES CN1CCN(Cc2ccc3Cc4c(n[nH]c4-c4ccsc4)-c3c2)CC1 Show InChI InChI=1S/C20H22N4S/c1-23-5-7-24(8-6-23)12-14-2-3-15-11-18-19(16-4-9-25-13-16)21-22-20(18)17(15)10-14/h2-4,9-10,13H,5-8,11-12H2,1H3,(H,21,22) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.57E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of FLT4 by HTRF assay |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188277
(6-((4-methylpiperazin-1-yl)methyl)-3-(thiazol-5-yl...)Show SMILES CN1CCN(Cc2ccc-3c(Cc4c-3n[nH]c4-c3cncs3)c2)CC1 Show InChI InChI=1S/C19H21N5S/c1-23-4-6-24(7-5-23)11-13-2-3-15-14(8-13)9-16-18(15)21-22-19(16)17-10-20-12-25-17/h2-3,8,10,12H,4-7,9,11H2,1H3,(H,21,22) | 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 | 2.84E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188289
(3-(3-((4-methylpiperazin-1-yl)methyl)phenyl)-1,4-d...)Show SMILES CN1CCN(Cc2cccc(c2)-c2[nH]nc-3c2Cc2ccccc-32)CC1 Show InChI InChI=1S/C22H24N4/c1-25-9-11-26(12-10-25)15-16-5-4-7-18(13-16)21-20-14-17-6-2-3-8-19(17)22(20)24-23-21/h2-8,13H,9-12,14-15H2,1H3,(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 | 3.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188273
(6-((4-methylpiperazin-1-yl)methyl)-3-(5-methylthio...)Show SMILES CN1CCN(Cc2ccc-3c(Cc4c-3n[nH]c4-c3ccc(C)s3)c2)CC1 Show InChI InChI=1S/C21H24N4S/c1-14-3-6-19(26-14)21-18-12-16-11-15(4-5-17(16)20(18)22-23-21)13-25-9-7-24(2)8-10-25/h3-6,11H,7-10,12-13H2,1-2H3,(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 | 5.47E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188274
(6-((4-methylpiperazin-1-yl)methyl)-3-(thiazol-4-yl...)Show SMILES CN1CCN(Cc2ccc-3c(Cc4c-3n[nH]c4-c3cscn3)c2)CC1 Show InChI InChI=1S/C19H21N5S/c1-23-4-6-24(7-5-23)10-13-2-3-15-14(8-13)9-16-18(15)21-22-19(16)17-11-25-12-20-17/h2-3,8,11-12H,4-7,9-10H2,1H3,(H,21,22) | 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 | 7.48E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188279
(6-((4-methylpiperazin-1-yl)methyl)-3-(pyridin-3-yl...)Show SMILES CN1CCN(Cc2ccc-3c(Cc4c(n[nH]c-34)-c3cccnc3)c2)CC1 Show InChI InChI=1S/C21H23N5/c1-25-7-9-26(10-8-25)14-15-4-5-18-17(11-15)12-19-20(23-24-21(18)19)16-3-2-6-22-13-16/h2-6,11,13H,7-10,12,14H2,1H3,(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 | 9.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188265
(6-((4-methylpiperazin-1-yl)methyl)-3-(4-methylthio...)Show SMILES CN1CCN(Cc2ccc-3c(Cc4c-3n[nH]c4-c3cc(C)cs3)c2)CC1 Show InChI InChI=1S/C21H24N4S/c1-14-9-19(26-13-14)21-18-11-16-10-15(3-4-17(16)20(18)22-23-21)12-25-7-5-24(2)6-8-25/h3-4,9-10,13H,5-8,11-12H2,1-2H3,(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 | 1.25E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188268
(5-((4-methylpiperazin-1-yl)methyl)-3-phenyl-1,4-di...)Show SMILES CN1CCN(Cc2cccc-3c2Cc2c-3[nH]nc2-c2ccccc2)CC1 Show InChI InChI=1S/C22H24N4/c1-25-10-12-26(13-11-25)15-17-8-5-9-18-19(17)14-20-21(23-24-22(18)20)16-6-3-2-4-7-16/h2-9H,10-15H2,1H3,(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 | 1.41E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188287
(6-((4-methylpiperazin-1-yl)methyl)-3-(thiazol-2-yl...)Show SMILES CN1CCN(Cc2ccc-3c(Cc4c(n[nH]c-34)-c3nccs3)c2)CC1 Show InChI InChI=1S/C19H21N5S/c1-23-5-7-24(8-6-23)12-13-2-3-15-14(10-13)11-16-17(15)21-22-18(16)19-20-4-9-25-19/h2-4,9-10H,5-8,11-12H2,1H3,(H,21,22) | 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 | 1.66E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Angiopoietin-1 receptor
(Homo sapiens (Human)) | BDBM50188272
(7-((1H-imidazol-1-yl)methyl)-3-(thiophen-3-yl)-1,4...)Show InChI InChI=1S/C18H14N4S/c1-2-13-8-16-17(14-3-6-23-10-14)20-21-18(16)15(13)7-12(1)9-22-5-4-19-11-22/h1-7,10-11H,8-9H2,(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 | 1.76E+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 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50188272
(7-((1H-imidazol-1-yl)methyl)-3-(thiophen-3-yl)-1,4...)Show InChI InChI=1S/C18H14N4S/c1-2-13-8-16-17(14-3-6-23-10-14)20-21-18(16)15(13)7-12(1)9-22-5-4-19-11-22/h1-7,10-11H,8-9H2,(H,20,21) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.11E+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 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Fibroblast growth factor receptor 1/2/3/4
(Homo sapiens (Human)) | BDBM50188272
(7-((1H-imidazol-1-yl)methyl)-3-(thiophen-3-yl)-1,4...)Show InChI InChI=1S/C18H14N4S/c1-2-13-8-16-17(14-3-6-23-10-14)20-21-18(16)15(13)7-12(1)9-22-5-4-19-11-22/h1-7,10-11H,8-9H2,(H,20,21) | PDB
UniProtKB/SwissProt
antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 3.44E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of FGFR by HTRF assay |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Angiopoietin-1 receptor
(Homo sapiens (Human)) | BDBM50188266
(7-((4-methylpiperazin-1-yl)methyl)-3-(thiophen-3-y...)Show SMILES CN1CCN(Cc2ccc3Cc4c(n[nH]c4-c4ccsc4)-c3c2)CC1 Show InChI InChI=1S/C20H22N4S/c1-23-5-7-24(8-6-23)12-14-2-3-15-11-18-19(16-4-9-25-13-16)21-22-20(18)17(15)10-14/h2-4,9-10,13H,5-8,11-12H2,1H3,(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 | 4.78E+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 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50188272
(7-((1H-imidazol-1-yl)methyl)-3-(thiophen-3-yl)-1,4...)Show InChI InChI=1S/C18H14N4S/c1-2-13-8-16-17(14-3-6-23-10-14)20-21-18(16)15(13)7-12(1)9-22-5-4-19-11-22/h1-7,10-11H,8-9H2,(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 | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of EGFR by HTRF assay |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188278
(3-(benzo[b]thiophen-2-yl)-6-((4-methylpiperazin-1-...)Show SMILES CN1CCN(Cc2ccc-3c(Cc4c-3n[nH]c4-c3cc4ccccc4s3)c2)CC1 Show InChI InChI=1S/C24H24N4S/c1-27-8-10-28(11-9-27)15-16-6-7-19-18(12-16)13-20-23(19)25-26-24(20)22-14-17-4-2-3-5-21(17)29-22/h2-7,12,14H,8-11,13,15H2,1H3,(H,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 | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50188266
(7-((4-methylpiperazin-1-yl)methyl)-3-(thiophen-3-y...)Show SMILES CN1CCN(Cc2ccc3Cc4c(n[nH]c4-c4ccsc4)-c3c2)CC1 Show InChI InChI=1S/C20H22N4S/c1-23-5-7-24(8-6-23)12-14-2-3-15-11-18-19(16-4-9-25-13-16)21-22-20(18)17(15)10-14/h2-4,9-10,13H,5-8,11-12H2,1H3,(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 | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of cMet by HTRF assay |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50188272
(7-((1H-imidazol-1-yl)methyl)-3-(thiophen-3-yl)-1,4...)Show InChI InChI=1S/C18H14N4S/c1-2-13-8-16-17(14-3-6-23-10-14)20-21-18(16)15(13)7-12(1)9-22-5-4-19-11-22/h1-7,10-11H,8-9H2,(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 | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of cMet by HTRF assay |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50188266
(7-((4-methylpiperazin-1-yl)methyl)-3-(thiophen-3-y...)Show SMILES CN1CCN(Cc2ccc3Cc4c(n[nH]c4-c4ccsc4)-c3c2)CC1 Show InChI InChI=1S/C20H22N4S/c1-23-5-7-24(8-6-23)12-14-2-3-15-11-18-19(16-4-9-25-13-16)21-22-20(18)17(15)10-14/h2-4,9-10,13H,5-8,11-12H2,1H3,(H,21,22) | 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 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188291
(6-((4-methylpiperazin-1-yl)methyl)-3-(3-methylthio...)Show SMILES CN1CCN(Cc2ccc-3c(Cc4c-3n[nH]c4-c3sccc3C)c2)CC1 Show InChI InChI=1S/C21H24N4S/c1-14-5-10-26-21(14)20-18-12-16-11-15(3-4-17(16)19(18)22-23-20)13-25-8-6-24(2)7-9-25/h3-5,10-11H,6-9,12-13H2,1-2H3,(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 | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Platelet-derived growth factor receptor alpha/beta
(Homo sapiens (Human)) | BDBM50188272
(7-((1H-imidazol-1-yl)methyl)-3-(thiophen-3-yl)-1,4...)Show InChI InChI=1S/C18H14N4S/c1-2-13-8-16-17(14-3-6-23-10-14)20-21-18(16)15(13)7-12(1)9-22-5-4-19-11-22/h1-7,10-11H,8-9H2,(H,20,21) | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia 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 PDGFR by HTRF assay |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Platelet-derived growth factor receptor alpha/beta
(Homo sapiens (Human)) | BDBM50188266
(7-((4-methylpiperazin-1-yl)methyl)-3-(thiophen-3-y...)Show SMILES CN1CCN(Cc2ccc3Cc4c(n[nH]c4-c4ccsc4)-c3c2)CC1 Show InChI InChI=1S/C20H22N4S/c1-23-5-7-24(8-6-23)12-14-2-3-15-11-18-19(16-4-9-25-13-16)21-22-20(18)17(15)10-14/h2-4,9-10,13H,5-8,11-12H2,1H3,(H,21,22) | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia 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 PDGFR by HTRF assay |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Fibroblast growth factor receptor 1/2/3/4
(Homo sapiens (Human)) | BDBM50188266
(7-((4-methylpiperazin-1-yl)methyl)-3-(thiophen-3-y...)Show SMILES CN1CCN(Cc2ccc3Cc4c(n[nH]c4-c4ccsc4)-c3c2)CC1 Show InChI InChI=1S/C20H22N4S/c1-23-5-7-24(8-6-23)12-14-2-3-15-11-18-19(16-4-9-25-13-16)21-22-20(18)17(15)10-14/h2-4,9-10,13H,5-8,11-12H2,1H3,(H,21,22) | PDB
UniProtKB/SwissProt
antibodypedia antibodypedia antibodypedia 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 FGFR by HTRF assay |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50188266
(7-((4-methylpiperazin-1-yl)methyl)-3-(thiophen-3-y...)Show SMILES CN1CCN(Cc2ccc3Cc4c(n[nH]c4-c4ccsc4)-c3c2)CC1 Show InChI InChI=1S/C20H22N4S/c1-23-5-7-24(8-6-23)12-14-2-3-15-11-18-19(16-4-9-25-13-16)21-22-20(18)17(15)10-14/h2-4,9-10,13H,5-8,11-12H2,1H3,(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 | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of EGFR by HTRF assay |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188286
(7-((1H-1,2,4-triazol-1-yl)methyl)-3-(thiophen-3-yl...)Show InChI InChI=1S/C17H13N5S/c1-2-12-6-15-16(13-3-4-23-8-13)20-21-17(15)14(12)5-11(1)7-22-10-18-9-19-22/h1-5,8-10H,6-7H2,(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 | 1.08E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188276
(7-(2-(4-methylpiperazin-1-yl)ethyl)-3-(thiophen-3-...)Show SMILES CN1CCN(CCc2ccc3Cc4c(n[nH]c4-c4ccsc4)-c3c2)CC1 Show InChI InChI=1S/C21H24N4S/c1-24-7-9-25(10-8-24)6-4-15-2-3-16-13-19-20(17-5-11-26-14-17)22-23-21(19)18(16)12-15/h2-3,5,11-12,14H,4,6-10,13H2,1H3,(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 | 1.43E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188272
(7-((1H-imidazol-1-yl)methyl)-3-(thiophen-3-yl)-1,4...)Show InChI InChI=1S/C18H14N4S/c1-2-13-8-16-17(14-3-6-23-10-14)20-21-18(16)15(13)7-12(1)9-22-5-4-19-11-22/h1-7,10-11H,8-9H2,(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 | 1.47E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of KDR-mediated biotin-Ahx-AEEEYFFLFA-amide substrate phosphorylation in presence of 1 mM ATP by HTRF assay |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188285
(7-((4-isopropylpiperazin-1-yl)methyl)-3-(thiophen-...)Show SMILES CC(C)N1CCN(Cc2ccc3Cc4c(n[nH]c4-c4ccsc4)-c3c2)CC1 Show InChI InChI=1S/C22H26N4S/c1-15(2)26-8-6-25(7-9-26)13-16-3-4-17-12-20-21(18-5-10-27-14-18)23-24-22(20)19(17)11-16/h3-5,10-11,14-15H,6-9,12-13H2,1-2H3,(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 | 1.90E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188282
(7-((1H-1,2,3-triazol-1-yl)methyl)-3-(thiophen-3-yl...)Show InChI InChI=1S/C17H13N5S/c1-2-12-8-15-16(13-3-6-23-10-13)19-20-17(15)14(12)7-11(1)9-22-5-4-18-21-22/h1-7,10H,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 | 1.90E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188280
(4-((3-(thiophen-3-yl)-1,4-dihydroindeno[1,2-c]pyra...)Show SMILES O=CN1CCN(Cc2ccc3Cc4c(n[nH]c4-c4ccsc4)-c3c2)CC1 Show InChI InChI=1S/C20H20N4OS/c25-13-24-6-4-23(5-7-24)11-14-1-2-15-10-18-19(16-3-8-26-12-16)21-22-20(18)17(15)9-14/h1-3,8-9,12-13H,4-7,10-11H2,(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 | 6.65E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188270
(CHEMBL213531 | N-ethyl-N-((3-(thiophen-3-yl)-1,4-d...)Show InChI InChI=1S/C19H21N3S/c1-3-22(4-2)11-13-5-6-14-10-17-18(15-7-8-23-12-15)20-21-19(17)16(14)9-13/h5-9,12H,3-4,10-11H2,1-2H3,(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 | 8.24E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188288
(6-(4-methylpiperazin-1-yl)-3-(thiophen-2-yl)-1,4-d...)Show SMILES CN1CCN(CC1)c1ccc-2c(Cc3c-2n[nH]c3-c2cccs2)c1 Show InChI InChI=1S/C19H20N4S/c1-22-6-8-23(9-7-22)14-4-5-15-13(11-14)12-16-18(15)20-21-19(16)17-3-2-10-24-17/h2-5,10-11H,6-9,12H2,1H3,(H,20,21) | 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 | 1.01E+6 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50188267
((4-methylpiperazin-1-yl)(3-(thiophen-3-yl)-1,4-dih...)Show SMILES CN1CCN(CC1)C(=O)c1ccc2Cc3c(n[nH]c3-c3ccsc3)-c2c1 Show InChI InChI=1S/C20H20N4OS/c1-23-5-7-24(8-6-23)20(25)14-3-2-13-10-17-18(15-4-9-26-12-15)21-22-19(17)16(13)11-14/h2-4,9,11-12H,5-8,10H2,1H3,(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 | 4.08E+6 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation transfected in NIH3T3 cells by ELISA |
Bioorg Med Chem Lett 16: 4371-5 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.052 BindingDB Entry DOI: 10.7270/Q2QJ7GX6 |
More data for this Ligand-Target Pair | |
Peroxisome proliferator-activated receptor alpha
(Homo sapiens (Human)) | BDBM50596499
(CHEMBL5185420)Show SMILES OC(=O)Cc1cccc(OCCC2CCN(CC2)c2nc3ccc(Cl)cc3s2)c1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | n/a | n/a | 2.22E+3 | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
Article DOI: 10.1016/j.bmcl.2022.128567 BindingDB Entry DOI: 10.7270/Q2KK9GV5 |
More data for this Ligand-Target Pair | |
Peroxisome proliferator-activated receptor alpha
(Homo sapiens (Human)) | BDBM28661
(2-{2-methyl-4-[({4-methyl-2-[4-(trifluoromethyl)ph...)Show SMILES Cc1nc(sc1CSc1ccc(OCC(O)=O)c(C)c1)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C21H18F3NO3S2/c1-12-9-16(7-8-17(12)28-10-19(26)27)29-11-18-13(2)25-20(30-18)14-3-5-15(6-4-14)21(22,23)24/h3-9H,10-11H2,1-2H3,(H,26,27) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL DrugBank MCE PC cid PC sid PDB UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 2.20E+3 | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
Article DOI: 10.1016/j.bmcl.2022.128567 BindingDB Entry DOI: 10.7270/Q2KK9GV5 |
More data for this Ligand-Target Pair | |
Peroxisome proliferator-activated receptor alpha
(Homo sapiens (Human)) | BDBM50596500
(CHEMBL5180073)Show SMILES Cc1ccc(CC(O)=O)cc1OCCC1CCN(CC1)c1nc2ccc(Cl)cc2s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | n/a | n/a | 637 | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
Article DOI: 10.1016/j.bmcl.2022.128567 BindingDB Entry DOI: 10.7270/Q2KK9GV5 |
More data for this Ligand-Target Pair | |