Found 98 hits with Last Name = 'kussie' and Initial = 'p' 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 2
(Homo sapiens (Human)) | BDBM50179883
((4-Isopropylphenyl)-(4-isoquinolin-5-yl-phthalazin...)Show SMILES CC(C)c1ccc(Nc2nnc(-c3cccc4cnccc34)c3ccccc23)cc1 Show InChI InChI=1S/C26H22N4/c1-17(2)18-10-12-20(13-11-18)28-26-24-8-4-3-7-23(24)25(29-30-26)22-9-5-6-19-16-27-15-14-21(19)22/h3-17H,1-2H3,(H,28,30) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 17 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems, Inc.
Curated by ChEMBL
| Assay Description Inhibition of VEGFR2 (unknown origin) by HTRF method |
Bioorg Med Chem 17: 731-40 (2009)
Article DOI: 10.1016/j.bmc.2008.11.049 BindingDB Entry DOI: 10.7270/Q2W95929 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM21
(CHEMBL24828 | N-(4-bromo-2-fluorophenyl)-6-methoxy...)Show SMILES COc1cc2c(Nc3ccc(Br)cc3F)ncnc2cc1OCC1CCN(C)CC1 Show InChI InChI=1S/C22H24BrFN4O2/c1-28-7-5-14(6-8-28)12-30-21-11-19-16(10-20(21)29-2)22(26-13-25-19)27-18-4-3-15(23)9-17(18)24/h3-4,9-11,13-14H,5-8,12H2,1-2H3,(H,25,26,27) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL DrugBank MCE PC cid PC sid PDB UniChem
Similars
| Article PubMed
| n/a | n/a | 45 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems, Inc.
Curated by ChEMBL
| Assay Description Inhibition of VEGFR2 (unknown origin) by HTRF method |
Bioorg Med Chem 17: 731-40 (2009)
Article DOI: 10.1016/j.bmc.2008.11.049 BindingDB Entry DOI: 10.7270/Q2W95929 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50179881
((4-Chlorophenyl)-(4-isoquinolin-5-yl-phthalazin-1-...)Show SMILES Clc1ccc(Nc2nnc(-c3cccc4cnccc34)c3ccccc23)cc1 Show InChI InChI=1S/C23H15ClN4/c24-16-8-10-17(11-9-16)26-23-21-6-2-1-5-20(21)22(27-28-23)19-7-3-4-15-14-25-13-12-18(15)19/h1-14H,(H,26,28) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 48 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems, Inc.
Curated by ChEMBL
| Assay Description Inhibition of VEGFR2 (unknown origin) by HTRF method |
Bioorg Med Chem 17: 731-40 (2009)
Article DOI: 10.1016/j.bmc.2008.11.049 BindingDB Entry DOI: 10.7270/Q2W95929 |
More data for this Ligand-Target Pair | |
Heparanase
(Homo sapiens (Human)) | BDBM50175932
(1,3-bis-[4-(5,6-dimethyl-1H-benzoimidazol-2-yl)phe...)Show SMILES Cc1cc2nc([nH]c2cc1C)-c1ccc(NC(=O)Nc2ccc(cc2)-c2nc3cc(C)c(C)cc3[nH]2)cc1 Show InChI InChI=1S/C31H28N6O/c1-17-13-25-26(14-18(17)2)35-29(34-25)21-5-9-23(10-6-21)32-31(38)33-24-11-7-22(8-12-24)30-36-27-15-19(3)20(4)16-28(27)37-30/h5-16H,1-4H3,(H,34,35)(H,36,37)(H2,32,33,38) | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 75 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against heparanase from human platelets |
Bioorg Med Chem Lett 16: 409-12 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.069 BindingDB Entry DOI: 10.7270/Q2ST7PDB |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50179890
((4-tert-Butylphenyl)-(4-isoquinolin-5-yl-phthalazi...)Show SMILES CC(C)(C)c1ccc(Nc2nnc(-c3cccc4cnccc34)c3ccccc23)cc1 Show InChI InChI=1S/C27H24N4/c1-27(2,3)19-11-13-20(14-12-19)29-26-24-9-5-4-8-23(24)25(30-31-26)22-10-6-7-18-17-28-16-15-21(18)22/h4-17H,1-3H3,(H,29,31) | 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 | 75 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems, Inc.
Curated by ChEMBL
| Assay Description Inhibition of VEGFR2 (unknown origin) by HTRF method |
Bioorg Med Chem 17: 731-40 (2009)
Article DOI: 10.1016/j.bmc.2008.11.049 BindingDB Entry DOI: 10.7270/Q2W95929 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50173019
(4-(4-(4-tert-butylphenylamino)phthalazin-1-yl)benz...)Show SMILES CC(C)(C)c1ccc(Nc2nnc(-c3ccc(cc3)C(N)=O)c3ccccc23)cc1 Show InChI InChI=1S/C25H24N4O/c1-25(2,3)18-12-14-19(15-13-18)27-24-21-7-5-4-6-20(21)22(28-29-24)16-8-10-17(11-9-16)23(26)30/h4-15H,1-3H3,(H2,26,30)(H,27,29) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 78 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems, Inc.
Curated by ChEMBL
| Assay Description Inhibition of VEGFR2 (unknown origin) by HTRF method |
Bioorg Med Chem 17: 731-40 (2009)
Article DOI: 10.1016/j.bmc.2008.11.049 BindingDB Entry DOI: 10.7270/Q2W95929 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50179889
(CHEMBL382818 | N-(4-(chlorodifluoromethoxy)phenyl)...)Show SMILES FC(F)(Cl)Oc1ccc(Nc2nnc(-c3cccc4cnccc34)c3ccccc23)cc1 Show InChI InChI=1S/C24H15ClF2N4O/c25-24(26,27)32-17-10-8-16(9-11-17)29-23-21-6-2-1-5-20(21)22(30-31-23)19-7-3-4-15-14-28-13-12-18(15)19/h1-14H,(H,29,31) | 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 | 79 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems, Inc.
Curated by ChEMBL
| Assay Description Inhibition of VEGFR2 (unknown origin) by HTRF method |
Bioorg Med Chem 17: 731-40 (2009)
Article DOI: 10.1016/j.bmc.2008.11.049 BindingDB Entry DOI: 10.7270/Q2W95929 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50173031
(4-(4-(4-bromophenylamino)phthalazin-1-yl)benzamide...)Show SMILES NC(=O)c1ccc(cc1)-c1nnc(Nc2ccc(Br)cc2)c2ccccc12 Show InChI InChI=1S/C21H15BrN4O/c22-15-9-11-16(12-10-15)24-21-18-4-2-1-3-17(18)19(25-26-21)13-5-7-14(8-6-13)20(23)27/h1-12H,(H2,23,27)(H,24,26) | 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 | 100 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems, Inc.
Curated by ChEMBL
| Assay Description Inhibition of VEGFR2 (unknown origin) by HTRF method |
Bioorg Med Chem 17: 731-40 (2009)
Article DOI: 10.1016/j.bmc.2008.11.049 BindingDB Entry DOI: 10.7270/Q2W95929 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50179888
((3,4-Dichloro-phenyl)-(4-isoquinolin-5-yl-phthalaz...)Show SMILES Clc1ccc(Nc2nnc(-c3cccc4cnccc34)c3ccccc23)cc1Cl Show InChI InChI=1S/C23H14Cl2N4/c24-20-9-8-15(12-21(20)25)27-23-19-6-2-1-5-18(19)22(28-29-23)17-7-3-4-14-13-26-11-10-16(14)17/h1-13H,(H,27,29) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 110 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems, Inc.
Curated by ChEMBL
| Assay Description Inhibition of VEGFR2 (unknown origin) by HTRF method |
Bioorg Med Chem 17: 731-40 (2009)
Article DOI: 10.1016/j.bmc.2008.11.049 BindingDB Entry DOI: 10.7270/Q2W95929 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50179891
((4-Chloro-3-trifluoromethylphenyl)-(4-isoquinolin-...)Show SMILES FC(F)(F)c1cc(Nc2nnc(-c3cccc4cnccc34)c3ccccc23)ccc1Cl Show InChI InChI=1S/C24H14ClF3N4/c25-21-9-8-15(12-20(21)24(26,27)28)30-23-19-6-2-1-5-18(19)22(31-32-23)17-7-3-4-14-13-29-11-10-16(14)17/h1-13H,(H,30,32) | 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 | 120 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems, Inc.
Curated by ChEMBL
| Assay Description Inhibition of VEGFR2 (unknown origin) by HTRF method |
Bioorg Med Chem 17: 731-40 (2009)
Article DOI: 10.1016/j.bmc.2008.11.049 BindingDB Entry DOI: 10.7270/Q2W95929 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50173045
(4-(4-(4-tert-butylphenylamino)phthalazin-1-yl)-N-m...)Show SMILES CNC(=O)c1ccc(cc1)-c1nnc(Nc2ccc(cc2)C(C)(C)C)c2ccccc12 Show InChI InChI=1S/C26H26N4O/c1-26(2,3)19-13-15-20(16-14-19)28-24-22-8-6-5-7-21(22)23(29-30-24)17-9-11-18(12-10-17)25(31)27-4/h5-16H,1-4H3,(H,27,31)(H,28,30) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 130 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems, Inc.
Curated by ChEMBL
| Assay Description Inhibition of VEGFR2 (unknown origin) by HTRF method |
Bioorg Med Chem 17: 731-40 (2009)
Article DOI: 10.1016/j.bmc.2008.11.049 BindingDB Entry DOI: 10.7270/Q2W95929 |
More data for this Ligand-Target Pair | |
Heparanase
(Homo sapiens (Human)) | BDBM50175936
(1,3-bis(4-(6-methyl-1H-benzo[d]imidazol-2-yl)pheny...)Show SMILES Cc1ccc2nc([nH]c2c1)-c1ccc(NC(=O)Nc2ccc(cc2)-c2nc3ccc(C)cc3[nH]2)cc1 Show InChI InChI=1S/C29H24N6O/c1-17-3-13-23-25(15-17)34-27(32-23)19-5-9-21(10-6-19)30-29(36)31-22-11-7-20(8-12-22)28-33-24-14-4-18(2)16-26(24)35-28/h3-16H,1-2H3,(H,32,34)(H,33,35)(H2,30,31,36) | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 150 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against heparanase from human platelets |
Bioorg Med Chem Lett 16: 409-12 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.069 BindingDB Entry DOI: 10.7270/Q2ST7PDB |
More data for this Ligand-Target Pair | |
Heparanase
(Homo sapiens (Human)) | BDBM50175938
(1,3-bis(4-(7-methyl-1H-benzo[d]imidazol-2-yl)pheny...)Show SMILES Cc1cccc2[nH]c(nc12)-c1ccc(NC(=O)Nc2ccc(cc2)-c2nc3c(C)cccc3[nH]2)cc1 Show InChI InChI=1S/C29H24N6O/c1-17-5-3-7-23-25(17)34-27(32-23)19-9-13-21(14-10-19)30-29(36)31-22-15-11-20(12-16-22)28-33-24-8-4-6-18(2)26(24)35-28/h3-16H,1-2H3,(H,32,34)(H,33,35)(H2,30,31,36) | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 150 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against heparanase from human platelets |
Bioorg Med Chem Lett 16: 409-12 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.069 BindingDB Entry DOI: 10.7270/Q2ST7PDB |
More data for this Ligand-Target Pair | |
Heparanase
(Homo sapiens (Human)) | BDBM50175931
(1-(4-(1H-benzo[d]imidazol-2-yl)phenyl)-3-(4-(7-met...)Show SMILES Cc1cccc2[nH]c(nc12)-c1ccc(NC(=O)Nc2ccc(cc2)-c2nc3ccccc3[nH]2)cc1 Show InChI InChI=1S/C28H22N6O/c1-17-5-4-8-24-25(17)34-27(33-24)19-11-15-21(16-12-19)30-28(35)29-20-13-9-18(10-14-20)26-31-22-6-2-3-7-23(22)32-26/h2-16H,1H3,(H,31,32)(H,33,34)(H2,29,30,35) | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 150 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against heparanase from human platelets |
Bioorg Med Chem Lett 16: 409-12 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.069 BindingDB Entry DOI: 10.7270/Q2ST7PDB |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50173049
(4-(4-(4-(chlorodifluoromethoxy)phenylamino)phthala...)Show SMILES NC(=O)c1ccc(cc1)-c1nnc(Nc2ccc(OC(F)(F)Cl)cc2)c2ccccc12 Show InChI InChI=1S/C22H15ClF2N4O2/c23-22(24,25)31-16-11-9-15(10-12-16)27-21-18-4-2-1-3-17(18)19(28-29-21)13-5-7-14(8-6-13)20(26)30/h1-12H,(H2,26,30)(H,27,29) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
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 |
ImClone Systems, Inc.
Curated by ChEMBL
| Assay Description Inhibition of VEGFR2 (unknown origin) by HTRF method |
Bioorg Med Chem 17: 731-40 (2009)
Article DOI: 10.1016/j.bmc.2008.11.049 BindingDB Entry DOI: 10.7270/Q2W95929 |
More data for this Ligand-Target Pair | |
Heparanase
(Homo sapiens (Human)) | BDBM50175811
(CHEMBL200215 | N-(4-{[4-(1H-benzoimidazol-2-yl)phe...)Show SMILES COc1ccc(cc1Br)C(=O)Nc1ccc(CNc2ccc(cc2)-c2nc3ccccc3[nH]2)cc1 Show InChI InChI=1S/C28H23BrN4O2/c1-35-26-15-10-20(16-23(26)29)28(34)31-22-11-6-18(7-12-22)17-30-21-13-8-19(9-14-21)27-32-24-4-2-3-5-25(24)33-27/h2-16,30H,17H2,1H3,(H,31,34)(H,32,33) | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 230 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against heparanase from human platelets |
Bioorg Med Chem Lett 16: 404-8 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.070 BindingDB Entry DOI: 10.7270/Q2FJ2G9R |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50179893
((4-Isoquinolin-5-yl-phthalazin-1-yl)-(2-methyl-1Hi...)Show SMILES Cc1cc2cc(Nc3nnc(-c4cccc5cnccc45)c4ccccc34)ccc2[nH]1 Show InChI InChI=1S/C26H19N5/c1-16-13-18-14-19(9-10-24(18)28-16)29-26-23-7-3-2-6-22(23)25(30-31-26)21-8-4-5-17-15-27-12-11-20(17)21/h2-15,28H,1H3,(H,29,31) | 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 | 230 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems, Inc.
Curated by ChEMBL
| Assay Description Inhibition of VEGFR2 (unknown origin) by HTRF method |
Bioorg Med Chem 17: 731-40 (2009)
Article DOI: 10.1016/j.bmc.2008.11.049 BindingDB Entry DOI: 10.7270/Q2W95929 |
More data for this Ligand-Target Pair | |
Heparanase
(Homo sapiens (Human)) | BDBM50175939
(1,3-bis-[4-(1H-benzoimidazol-2-yl)phenyl]urea | CH...)Show SMILES O=C(Nc1ccc(cc1)-c1nc2ccccc2[nH]1)Nc1ccc(cc1)-c1nc2ccccc2[nH]1 Show InChI InChI=1S/C27H20N6O/c34-27(28-19-13-9-17(10-14-19)25-30-21-5-1-2-6-22(21)31-25)29-20-15-11-18(12-16-20)26-32-23-7-3-4-8-24(23)33-26/h1-16H,(H,30,31)(H,32,33)(H2,28,29,34) | PDB
KEGG
UniProtKB/SwissProt
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 |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against heparanase from human platelets |
Bioorg Med Chem Lett 16: 409-12 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.069 BindingDB Entry DOI: 10.7270/Q2ST7PDB |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50179884
((4-Isoquinolin-5-yl-phthalazin-1-yl)-m-tolylamine ...)Show SMILES Cc1cccc(Nc2nnc(-c3cccc4cnccc34)c3ccccc23)c1 Show InChI InChI=1S/C24H18N4/c1-16-6-4-8-18(14-16)26-24-22-10-3-2-9-21(22)23(27-28-24)20-11-5-7-17-15-25-13-12-19(17)20/h2-15H,1H3,(H,26,28) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 270 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems, Inc.
Curated by ChEMBL
| Assay Description Inhibition of VEGFR2 (unknown origin) by HTRF method |
Bioorg Med Chem 17: 731-40 (2009)
Article DOI: 10.1016/j.bmc.2008.11.049 BindingDB Entry DOI: 10.7270/Q2W95929 |
More data for this Ligand-Target Pair | |
Heparanase
(Homo sapiens (Human)) | BDBM50175813
(CHEMBL200831 | N-(4-{[5-(1H-benzoimidazol-2-yl)-py...)Show SMILES COc1ccc(cc1Br)C(=O)Nc1ccc(CNc2ccc(cn2)-c2nc3ccccc3[nH]2)cc1 Show InChI InChI=1S/C27H22BrN5O2/c1-35-24-12-8-18(14-21(24)28)27(34)31-20-10-6-17(7-11-20)15-29-25-13-9-19(16-30-25)26-32-22-4-2-3-5-23(22)33-26/h2-14,16H,15H2,1H3,(H,29,30)(H,31,34)(H,32,33) | PDB
KEGG
UniProtKB/SwissProt
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 |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against heparanase from human platelets |
Bioorg Med Chem Lett 16: 404-8 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.070 BindingDB Entry DOI: 10.7270/Q2FJ2G9R |
More data for this Ligand-Target Pair | |
Aurora kinase A
(Homo sapiens (Human)) | BDBM50174697
(3-fluoro-N-[5-(7-methoxy-10,11-dihydro-5-oxa-2,4,1...)Show SMILES COc1ccc2CNc3c(Nc4cnc(NC(=O)c5cccc(F)c5)nc4)ncnc3Oc2c1 Show InChI InChI=1S/C23H18FN7O3/c1-33-17-6-5-14-9-25-19-20(28-12-29-22(19)34-18(14)8-17)30-16-10-26-23(27-11-16)31-21(32)13-3-2-4-15(24)7-13/h2-8,10-12,25H,9H2,1H3,(H,28,29,30)(H,26,27,31,32) | 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 | 320 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against Aurora A kinase |
Bioorg Med Chem Lett 15: 5474-7 (2005)
Article DOI: 10.1016/j.bmcl.2005.08.098 BindingDB Entry DOI: 10.7270/Q2S46RGS |
More data for this Ligand-Target Pair | |
Aurora kinase A
(Homo sapiens (Human)) | BDBM50174698
(4-fluoro-N-[5-(7-methoxy-10,11-dihydro-5-oxa-2,4,1...)Show SMILES COc1ccc2CNc3c(Nc4cnc(NC(=O)c5ccc(F)cc5)nc4)ncnc3Oc2c1 Show InChI InChI=1S/C23H18FN7O3/c1-33-17-7-4-14-9-25-19-20(28-12-29-22(19)34-18(14)8-17)30-16-10-26-23(27-11-16)31-21(32)13-2-5-15(24)6-3-13/h2-8,10-12,25H,9H2,1H3,(H,28,29,30)(H,26,27,31,32) | 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 | 330 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against Aurora A kinase |
Bioorg Med Chem Lett 15: 5474-7 (2005)
Article DOI: 10.1016/j.bmcl.2005.08.098 BindingDB Entry DOI: 10.7270/Q2S46RGS |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50179894
((4-Isoquinolin-5-yl-phthalazin-1-yl)-(4-morpholin-...)Show SMILES C1CN(CCO1)c1ccc(Nc2nnc(-c3cccc4cnccc34)c3ccccc23)cc1 Show InChI InChI=1S/C27H23N5O/c1-2-6-25-24(5-1)26(23-7-3-4-19-18-28-13-12-22(19)23)30-31-27(25)29-20-8-10-21(11-9-20)32-14-16-33-17-15-32/h1-13,18H,14-17H2,(H,29,31) | 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 | 390 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems, Inc.
Curated by ChEMBL
| Assay Description Inhibition of VEGFR2 (unknown origin) by HTRF method |
Bioorg Med Chem 17: 731-40 (2009)
Article DOI: 10.1016/j.bmc.2008.11.049 BindingDB Entry DOI: 10.7270/Q2W95929 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50173022
(3-(4-(4-tert-butylphenylamino)phthalazin-1-yl)benz...)Show SMILES CC(C)(C)c1ccc(Nc2nnc(-c3cccc(c3)C(N)=O)c3ccccc23)cc1 Show InChI InChI=1S/C25H24N4O/c1-25(2,3)18-11-13-19(14-12-18)27-24-21-10-5-4-9-20(21)22(28-29-24)16-7-6-8-17(15-16)23(26)30/h4-15H,1-3H3,(H2,26,30)(H,27,29) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 400 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems, Inc.
Curated by ChEMBL
| Assay Description Inhibition of VEGFR2 (unknown origin) by HTRF method |
Bioorg Med Chem 17: 731-40 (2009)
Article DOI: 10.1016/j.bmc.2008.11.049 BindingDB Entry DOI: 10.7270/Q2W95929 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50179882
((2-Fluoro-4-methylphenyl)-(4-isoquinolin-5-ylphtha...)Show SMILES Cc1ccc(Nc2nnc(-c3cccc4cnccc34)c3ccccc23)c(F)c1 Show InChI InChI=1S/C24H17FN4/c1-15-9-10-22(21(25)13-15)27-24-20-7-3-2-6-19(20)23(28-29-24)18-8-4-5-16-14-26-12-11-17(16)18/h2-14H,1H3,(H,27,29) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 430 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems, Inc.
Curated by ChEMBL
| Assay Description Inhibition of VEGFR2 (unknown origin) by HTRF method |
Bioorg Med Chem 17: 731-40 (2009)
Article DOI: 10.1016/j.bmc.2008.11.049 BindingDB Entry DOI: 10.7270/Q2W95929 |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50174686
(1-(1-chloro-5-oxa-2,4,11-triaza-dibenzo[a,d]cycloh...)Show SMILES FC(F)(F)c1cc(NC(=O)Nc2ccc3Oc4ncnc(Cl)c4N=Cc3c2)ccc1Cl |c:24| Show InChI InChI=1S/C19H10Cl2F3N5O2/c20-13-3-1-11(6-12(13)19(22,23)24)29-18(30)28-10-2-4-14-9(5-10)7-25-15-16(21)26-8-27-17(15)31-14/h1-8H,(H2,28,29,30) | PDB
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 | 450 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against FLT3 kinase in a HTRF assay |
Bioorg Med Chem Lett 15: 5474-7 (2005)
Article DOI: 10.1016/j.bmcl.2005.08.098 BindingDB Entry DOI: 10.7270/Q2S46RGS |
More data for this Ligand-Target Pair | |
Aurora kinase A
(Homo sapiens (Human)) | BDBM50174689
(CHEMBL439512 | N-[5-(7,8-dimethoxy-10,11-dihydro-5...)Show SMILES COc1cc2CNc3c(Nc4cnc(NC(=O)c5ccccc5)nc4)ncnc3Oc2cc1OC Show InChI InChI=1S/C24H21N7O4/c1-33-18-8-15-10-25-20-21(28-13-29-23(20)35-17(15)9-19(18)34-2)30-16-11-26-24(27-12-16)31-22(32)14-6-4-3-5-7-14/h3-9,11-13,25H,10H2,1-2H3,(H,28,29,30)(H,26,27,31,32) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 470 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against Aurora A kinase |
Bioorg Med Chem Lett 15: 5474-7 (2005)
Article DOI: 10.1016/j.bmcl.2005.08.098 BindingDB Entry DOI: 10.7270/Q2S46RGS |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50173034
(4-(4-(3-tert-butylphenylamino)phthalazin-1-yl)benz...)Show SMILES CC(C)(C)c1cccc(Nc2nnc(-c3ccc(cc3)C(N)=O)c3ccccc23)c1 Show InChI InChI=1S/C25H24N4O/c1-25(2,3)18-7-6-8-19(15-18)27-24-21-10-5-4-9-20(21)22(28-29-24)16-11-13-17(14-12-16)23(26)30/h4-15H,1-3H3,(H2,26,30)(H,27,29) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 470 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems, Inc.
Curated by ChEMBL
| Assay Description Inhibition of VEGFR2 (unknown origin) by HTRF method |
Bioorg Med Chem 17: 731-40 (2009)
Article DOI: 10.1016/j.bmc.2008.11.049 BindingDB Entry DOI: 10.7270/Q2W95929 |
More data for this Ligand-Target Pair | |
Aurora kinase A
(Homo sapiens (Human)) | BDBM50174692
(CHEMBL200525 | N-[5-(7-methoxy-10,11-dihydro-5-oxa...)Show SMILES COc1ccc2CNc3c(Nc4cnc(NC(=O)c5ccccc5)nc4)ncnc3Oc2c1 Show InChI InChI=1S/C23H19N7O3/c1-32-17-8-7-15-10-24-19-20(27-13-28-22(19)33-18(15)9-17)29-16-11-25-23(26-12-16)30-21(31)14-5-3-2-4-6-14/h2-9,11-13,24H,10H2,1H3,(H,27,28,29)(H,25,26,30,31) | 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 | 600 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against Aurora A kinase |
Bioorg Med Chem Lett 15: 5474-7 (2005)
Article DOI: 10.1016/j.bmcl.2005.08.098 BindingDB Entry DOI: 10.7270/Q2S46RGS |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50173021
(4-{4-[4-(Chloro-difluoro-methoxy)-phenylamino]-pht...)Show SMILES COC(=O)c1ccc(cc1)-c1nnc(Nc2ccc(OC(F)(F)Cl)cc2)c2ccccc12 Show InChI InChI=1S/C23H16ClF2N3O3/c1-31-22(30)15-8-6-14(7-9-15)20-18-4-2-3-5-19(18)21(29-28-20)27-16-10-12-17(13-11-16)32-23(24,25)26/h2-13H,1H3,(H,27,29) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 630 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems, Inc.
Curated by ChEMBL
| Assay Description Inhibition of VEGFR2 (unknown origin) by HTRF method |
Bioorg Med Chem 17: 731-40 (2009)
Article DOI: 10.1016/j.bmc.2008.11.049 BindingDB Entry DOI: 10.7270/Q2W95929 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50173051
(4-(4-(3,4-dichlorophenylamino)phthalazin-1-yl)benz...)Show SMILES NC(=O)c1ccc(cc1)-c1nnc(Nc2ccc(Cl)c(Cl)c2)c2ccccc12 Show InChI InChI=1S/C21H14Cl2N4O/c22-17-10-9-14(11-18(17)23)25-21-16-4-2-1-3-15(16)19(26-27-21)12-5-7-13(8-6-12)20(24)28/h1-11H,(H2,24,28)(H,25,27) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 840 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems, Inc.
Curated by ChEMBL
| Assay Description Inhibition of VEGFR2 (unknown origin) by HTRF method |
Bioorg Med Chem 17: 731-40 (2009)
Article DOI: 10.1016/j.bmc.2008.11.049 BindingDB Entry DOI: 10.7270/Q2W95929 |
More data for this Ligand-Target Pair | |
Heparanase
(Homo sapiens (Human)) | BDBM50175937
(1,3-bis(4-(7-methoxy-1H-benzo[d]imidazol-2-yl)phen...)Show SMILES COc1cccc2[nH]c(nc12)-c1ccc(NC(=O)Nc2ccc(cc2)-c2nc3c(OC)cccc3[nH]2)cc1 Show InChI InChI=1S/C29H24N6O3/c1-37-23-7-3-5-21-25(23)34-27(32-21)17-9-13-19(14-10-17)30-29(36)31-20-15-11-18(12-16-20)28-33-22-6-4-8-24(38-2)26(22)35-28/h3-16H,1-2H3,(H,32,34)(H,33,35)(H2,30,31,36) | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 870 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against heparanase from human platelets |
Bioorg Med Chem Lett 16: 409-12 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.069 BindingDB Entry DOI: 10.7270/Q2ST7PDB |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50174701
(1-(3-chloro-10,11-dihydro-5-oxa-2,4,11-triaza-dibe...)Show SMILES FC(F)(F)c1cc(NC(=O)Nc2ccc3Oc4nc(Cl)ncc4NCc3c2)ccc1Cl Show InChI InChI=1S/C19H12Cl2F3N5O2/c20-13-3-1-11(6-12(13)19(22,23)24)28-18(30)27-10-2-4-15-9(5-10)7-25-14-8-26-17(21)29-16(14)31-15/h1-6,8,25H,7H2,(H2,27,28,30) | 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 | 900 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against FLT3 kinase in a HTRF assay |
Bioorg Med Chem Lett 15: 5474-7 (2005)
Article DOI: 10.1016/j.bmcl.2005.08.098 BindingDB Entry DOI: 10.7270/Q2S46RGS |
More data for this Ligand-Target Pair | |
Heparanase
(Homo sapiens (Human)) | BDBM50175933
(1,3-bis(4-(1H-imidazo[4,5-c]pyridin-2-yl)phenyl)ur...)Show SMILES O=C(Nc1ccc(cc1)-c1nc2ccncc2[nH]1)Nc1ccc(cc1)-c1nc2ccncc2[nH]1 Show InChI InChI=1S/C25H18N8O/c34-25(28-17-5-1-15(2-6-17)23-30-19-9-11-26-13-21(19)32-23)29-18-7-3-16(4-8-18)24-31-20-10-12-27-14-22(20)33-24/h1-14H,(H,30,32)(H,31,33)(H2,28,29,34) | PDB
KEGG
UniProtKB/SwissProt
DrugBank 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 |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against heparanase from human platelets |
Bioorg Med Chem Lett 16: 409-12 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.069 BindingDB Entry DOI: 10.7270/Q2ST7PDB |
More data for this Ligand-Target Pair | |
Heparanase
(Homo sapiens (Human)) | BDBM50175823
(CHEMBL199569 | N-{4-[4-(1H-benzoimidazol-2-yl)-phe...)Show SMILES COc1ccc(cc1Br)C(=O)Nc1ccc(cc1)C(=O)Nc1ccc(cc1)-c1nc2ccccc2[nH]1 Show InChI InChI=1S/C28H21BrN4O3/c1-36-25-15-10-19(16-22(25)29)28(35)31-21-13-8-18(9-14-21)27(34)30-20-11-6-17(7-12-20)26-32-23-4-2-3-5-24(23)33-26/h2-16H,1H3,(H,30,34)(H,31,35)(H,32,33) | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 910 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against heparanase from human platelets |
Bioorg Med Chem Lett 16: 404-8 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.070 BindingDB Entry DOI: 10.7270/Q2FJ2G9R |
More data for this Ligand-Target Pair | |
Heparanase
(Homo sapiens (Human)) | BDBM50175821
(CHEMBL200399 | N-(4-((4-(1H-imidazo[4,5-c]pyridin-...)Show SMILES COc1ccc(cc1Br)C(=O)Nc1ccc(CNc2ccc(cc2)-c2nc3ccncc3[nH]2)cc1 Show InChI InChI=1S/C27H22BrN5O2/c1-35-25-11-6-19(14-22(25)28)27(34)31-21-7-2-17(3-8-21)15-30-20-9-4-18(5-10-20)26-32-23-12-13-29-16-24(23)33-26/h2-14,16,30H,15H2,1H3,(H,31,34)(H,32,33) | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 930 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against heparanase from human platelets |
Bioorg Med Chem Lett 16: 404-8 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.070 BindingDB Entry DOI: 10.7270/Q2FJ2G9R |
More data for this Ligand-Target Pair | |
Heparanase
(Homo sapiens (Human)) | BDBM50175822
(1-(4-(1H-benzo[d]imidazol-2-yl)phenyl)-3-(3-bromo-...)Show SMILES COc1ccc(NC(=O)Nc2ccc(cc2)-c2nc3ccccc3[nH]2)cc1Br Show InChI InChI=1S/C21H17BrN4O2/c1-28-19-11-10-15(12-16(19)22)24-21(27)23-14-8-6-13(7-9-14)20-25-17-4-2-3-5-18(17)26-20/h2-12H,1H3,(H,25,26)(H2,23,24,27) | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 930 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against heparanase from human platelets |
Bioorg Med Chem Lett 16: 404-8 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.070 BindingDB Entry DOI: 10.7270/Q2FJ2G9R |
More data for this Ligand-Target Pair | |
Aurora kinase A
(Homo sapiens (Human)) | BDBM50174690
(CHEMBL199547 | N-[5-(8-methoxy-10,11-dihydro-5-oxa...)Show SMILES COc1ccc2Oc3ncnc(Nc4cnc(NC(=O)c5ccccc5)nc4)c3NCc2c1 Show InChI InChI=1S/C23H19N7O3/c1-32-17-7-8-18-15(9-17)10-24-19-20(27-13-28-22(19)33-18)29-16-11-25-23(26-12-16)30-21(31)14-5-3-2-4-6-14/h2-9,11-13,24H,10H2,1H3,(H,27,28,29)(H,25,26,30,31) | 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 | 970 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against Aurora A kinase |
Bioorg Med Chem Lett 15: 5474-7 (2005)
Article DOI: 10.1016/j.bmcl.2005.08.098 BindingDB Entry DOI: 10.7270/Q2S46RGS |
More data for this Ligand-Target Pair | |
Heparanase
(Homo sapiens (Human)) | BDBM50175934
(1-(4-(1H-benzo[d]imidazol-2-yl)phenyl)-3-(4-(1H-im...)Show SMILES O=C(Nc1ccc(cc1)-c1nc2ccccc2[nH]1)Nc1ccc(cc1)-c1nc2ncccc2[nH]1 Show InChI InChI=1S/C26H19N7O/c34-26(28-18-11-7-16(8-12-18)23-30-20-4-1-2-5-21(20)31-23)29-19-13-9-17(10-14-19)24-32-22-6-3-15-27-25(22)33-24/h1-15H,(H,30,31)(H,27,32,33)(H2,28,29,34) | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against heparanase from human platelets |
Bioorg Med Chem Lett 16: 409-12 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.069 BindingDB Entry DOI: 10.7270/Q2ST7PDB |
More data for this Ligand-Target Pair | |
Heparanase
(Homo sapiens (Human)) | BDBM50175803
(3-bromo-N-(4-(5,6-dimethyl-1H-benzo[d]imidazol-2-y...)Show SMILES CCOc1ccc(cc1Br)C(=O)Nc1ccc(cc1)-c1nc2cc(C)c(C)cc2[nH]1 Show InChI InChI=1S/C24H22BrN3O2/c1-4-30-22-10-7-17(13-19(22)25)24(29)26-18-8-5-16(6-9-18)23-27-20-11-14(2)15(3)12-21(20)28-23/h5-13H,4H2,1-3H3,(H,26,29)(H,27,28) | PDB
KEGG
UniProtKB/SwissProt
DrugBank 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 |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against heparanase from human platelets |
Bioorg Med Chem Lett 16: 404-8 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.070 BindingDB Entry DOI: 10.7270/Q2FJ2G9R |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50173024
(4-(4-(4-(chlorodifluoromethoxy)phenylamino)phthala...)Show SMILES OCCNC(=O)c1ccc(cc1)-c1nnc(Nc2ccc(OC(F)(F)Cl)cc2)c2ccccc12 Show InChI InChI=1S/C24H19ClF2N4O3/c25-24(26,27)34-18-11-9-17(10-12-18)29-22-20-4-2-1-3-19(20)21(30-31-22)15-5-7-16(8-6-15)23(33)28-13-14-32/h1-12,32H,13-14H2,(H,28,33)(H,29,31) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL KEGG 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 |
ImClone Systems, Inc.
Curated by ChEMBL
| Assay Description Inhibition of VEGFR2 (unknown origin) by HTRF method |
Bioorg Med Chem 17: 731-40 (2009)
Article DOI: 10.1016/j.bmc.2008.11.049 BindingDB Entry DOI: 10.7270/Q2W95929 |
More data for this Ligand-Target Pair | |
Aurora kinase A
(Homo sapiens (Human)) | BDBM50174694
(CHEMBL371937 | N-[5-(7,8-dimethoxy-10,11-dihydro-5...)Show SMILES COc1cc2CNc3c(Nc4cnc(NC(=O)c5cccc(F)c5)nc4)ncnc3Oc2cc1OC Show InChI InChI=1S/C24H20FN7O4/c1-34-18-7-14-9-26-20-21(29-12-30-23(20)36-17(14)8-19(18)35-2)31-16-10-27-24(28-11-16)32-22(33)13-4-3-5-15(25)6-13/h3-8,10-12,26H,9H2,1-2H3,(H,29,30,31)(H,27,28,32,33) | 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 | 1.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against Aurora A kinase |
Bioorg Med Chem Lett 15: 5474-7 (2005)
Article DOI: 10.1016/j.bmcl.2005.08.098 BindingDB Entry DOI: 10.7270/Q2S46RGS |
More data for this Ligand-Target Pair | |
Aurora kinase A
(Homo sapiens (Human)) | BDBM50174691
(3-fluoro-N-[5-(8-methoxy-10,11-dihydro-5-oxa-2,4,1...)Show SMILES COc1ccc2Oc3ncnc(Nc4cnc(NC(=O)c5cccc(F)c5)nc4)c3NCc2c1 Show InChI InChI=1S/C23H18FN7O3/c1-33-17-5-6-18-14(8-17)9-25-19-20(28-12-29-22(19)34-18)30-16-10-26-23(27-11-16)31-21(32)13-3-2-4-15(24)7-13/h2-8,10-12,25H,9H2,1H3,(H,28,29,30)(H,26,27,31,32) | 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 | 1.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against Aurora A kinase |
Bioorg Med Chem Lett 15: 5474-7 (2005)
Article DOI: 10.1016/j.bmcl.2005.08.098 BindingDB Entry DOI: 10.7270/Q2S46RGS |
More data for this Ligand-Target Pair | |
Heparanase
(Homo sapiens (Human)) | BDBM50175930
(1-(4-(1H-benzo[d]imidazol-2-yl)phenyl)-3-(4-(7-met...)Show SMILES COc1cccc2[nH]c(nc12)-c1ccc(NC(=O)Nc2ccc(cc2)-c2nc3ccccc3[nH]2)cc1 Show InChI InChI=1S/C28H22N6O2/c1-36-24-8-4-7-23-25(24)34-27(33-23)18-11-15-20(16-12-18)30-28(35)29-19-13-9-17(10-14-19)26-31-21-5-2-3-6-22(21)32-26/h2-16H,1H3,(H,31,32)(H,33,34)(H2,29,30,35) | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.15E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against heparanase from human platelets |
Bioorg Med Chem Lett 16: 409-12 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.069 BindingDB Entry DOI: 10.7270/Q2ST7PDB |
More data for this Ligand-Target Pair | |
Heparanase
(Homo sapiens (Human)) | BDBM50175819
(CHEMBL200745 | N-(4-(1H-benzo[d]imidazol-2-yl)phen...)Show SMILES CCOc1ccc(cc1Br)C(=O)Nc1ccc(cc1)-c1nc2ccccc2[nH]1 Show InChI InChI=1S/C22H18BrN3O2/c1-2-28-20-12-9-15(13-17(20)23)22(27)24-16-10-7-14(8-11-16)21-25-18-5-3-4-6-19(18)26-21/h3-13H,2H2,1H3,(H,24,27)(H,25,26) | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against heparanase from human platelets |
Bioorg Med Chem Lett 16: 404-8 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.070 BindingDB Entry DOI: 10.7270/Q2FJ2G9R |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50173041
(3,5-dimethoxy-N-(1-(naphthalen-2-ylmethyl)piperidi...)Show SMILES NC(=O)c1ccc(cc1)-c1nnc(Nc2cccc(Br)c2)c2ccccc12 Show InChI InChI=1S/C21H15BrN4O/c22-15-4-3-5-16(12-15)24-21-18-7-2-1-6-17(18)19(25-26-21)13-8-10-14(11-9-13)20(23)27/h1-12H,(H2,23,27)(H,24,26) | 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 | 1.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems, Inc.
Curated by ChEMBL
| Assay Description Inhibition of VEGFR2 (unknown origin) by HTRF method |
Bioorg Med Chem 17: 731-40 (2009)
Article DOI: 10.1016/j.bmc.2008.11.049 BindingDB Entry DOI: 10.7270/Q2W95929 |
More data for this Ligand-Target Pair | |
Aurora kinase A
(Homo sapiens (Human)) | BDBM50174700
(CHEMBL199950 | N-[5-(7,8-dimethoxy-10,11-dihydro-5...)Show SMILES COc1cc2CNc3c(Nc4cnc(NC(=O)c5ccc(C)cc5)nc4)ncnc3Oc2cc1OC Show InChI InChI=1S/C25H23N7O4/c1-14-4-6-15(7-5-14)23(33)32-25-27-11-17(12-28-25)31-22-21-24(30-13-29-22)36-18-9-20(35-3)19(34-2)8-16(18)10-26-21/h4-9,11-13,26H,10H2,1-3H3,(H,29,30,31)(H,27,28,32,33) | 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 | 1.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against Aurora A kinase |
Bioorg Med Chem Lett 15: 5474-7 (2005)
Article DOI: 10.1016/j.bmcl.2005.08.098 BindingDB Entry DOI: 10.7270/Q2S46RGS |
More data for this Ligand-Target Pair | |
Heparanase
(Homo sapiens (Human)) | BDBM50175807
(3-bromo-N-(4-(4,5-dimethyl-1H-benzo[d]imidazol-2-y...)Show SMILES CCOc1ccc(cc1Br)C(=O)Nc1ccc(cc1)-c1nc2ccc(C)c(C)c2[nH]1 Show InChI InChI=1S/C24H22BrN3O2/c1-4-30-21-12-8-17(13-19(21)25)24(29)26-18-9-6-16(7-10-18)23-27-20-11-5-14(2)15(3)22(20)28-23/h5-13H,4H2,1-3H3,(H,26,29)(H,27,28) | PDB
KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems Inc
Curated by ChEMBL
| Assay Description Inhibitory activity against heparanase from human platelets |
Bioorg Med Chem Lett 16: 404-8 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.070 BindingDB Entry DOI: 10.7270/Q2FJ2G9R |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50173011
(4-(4-(4-chlorophenylamino)phthalazin-1-yl)benzamid...)Show SMILES NC(=O)c1ccc(cc1)-c1nnc(Nc2ccc(Cl)cc2)c2ccccc12 Show InChI InChI=1S/C21H15ClN4O/c22-15-9-11-16(12-10-15)24-21-18-4-2-1-3-17(18)19(25-26-21)13-5-7-14(8-6-13)20(23)27/h1-12H,(H2,23,27)(H,24,26) | 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 | 1.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems, Inc.
Curated by ChEMBL
| Assay Description Inhibition of VEGFR2 (unknown origin) by HTRF method |
Bioorg Med Chem 17: 731-40 (2009)
Article DOI: 10.1016/j.bmc.2008.11.049 BindingDB Entry DOI: 10.7270/Q2W95929 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50173029
(4-(4-(m-tolylamino)phthalazin-1-yl)benzamide | 4-(...)Show SMILES Cc1cccc(Nc2nnc(-c3ccc(cc3)C(N)=O)c3ccccc23)c1 Show InChI InChI=1S/C22H18N4O/c1-14-5-4-6-17(13-14)24-22-19-8-3-2-7-18(19)20(25-26-22)15-9-11-16(12-10-15)21(23)27/h2-13H,1H3,(H2,23,27)(H,24,26) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
ImClone Systems, Inc.
Curated by ChEMBL
| Assay Description Inhibition of VEGFR2 (unknown origin) by HTRF method |
Bioorg Med Chem 17: 731-40 (2009)
Article DOI: 10.1016/j.bmc.2008.11.049 BindingDB Entry DOI: 10.7270/Q2W95929 |
More data for this Ligand-Target Pair | |