Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Vascular endothelial growth factor receptor 2' and Ligand = 'BDBM50243360'   

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))	BDBM50243360 (1-{4-[7-Amino-3-(1-methyl-1H-pyrazol-4-yl)pyrazolo...) Show SMILES Cc1cccc(NC(=O)Nc2ccc(cc2)-c2cnc3c(cnn3c2N)-c2cnn(C)c2)c1 Show InChI InChI=1S/C24H22N8O/c1-15-4-3-5-19(10-15)30-24(33)29-18-8-6-16(7-9-18)20-12-26-23-21(13-28-32(23)22(20)25)17-11-27-31(2)14-17/h3-14H,25H2,1-2H3,(H2,29,30,33)	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	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human KDR phosphorylation expressed in mouse NIH3T3 cells by ELISA				J Med Chem 51: 3777-87 (2008) Article DOI: 10.1021/jm701397k BindingDB Entry DOI: 10.7270/Q22R3RFW
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50243360 (1-{4-[7-Amino-3-(1-methyl-1H-pyrazol-4-yl)pyrazolo...) Show SMILES Cc1cccc(NC(=O)Nc2ccc(cc2)-c2cnc3c(cnn3c2N)-c2cnn(C)c2)c1 Show InChI InChI=1S/C24H22N8O/c1-15-4-3-5-19(10-15)30-24(33)29-18-8-6-16(7-9-18)20-12-26-23-21(13-28-32(23)22(20)25)17-11-27-31(2)14-17/h3-14H,25H2,1-2H3,(H2,29,30,33)	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	4	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of KDR (unknown origin) by HTRF assay				J Med Chem 51: 3777-87 (2008) Article DOI: 10.1021/jm701397k BindingDB Entry DOI: 10.7270/Q22R3RFW
					More data for this Ligand-Target Pair