Compile Data Set for Download or QSAR

Found 1 hit Enz. Inhib. hit(s) with Target = 'Focal adhesion kinase 1' and Ligand = 'BDBM50181967'   

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
Focal adhesion kinase 1 (Homo sapiens (Human))	BDBM50181967 (8-(pyridin-2-yl)-2-(3,4,5-trimethoxyphenylamino)-5...) Show SMILES COc1cc(Nc2ncc3CCC(=O)N(c4ccccn4)c3n2)cc(OC)c1OC Show InChI InChI=1S/C21H21N5O4/c1-28-15-10-14(11-16(29-2)19(15)30-3)24-21-23-12-13-7-8-18(27)26(20(13)25-21)17-6-4-5-9-22-17/h4-6,9-12H,7-8H2,1-3H3,(H,23,24,25)	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	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Genomics Institute of the Novartis Research Foundation (GNF) Curated by ChEMBL					Assay Description Inhibitory activity against FAK				Bioorg Med Chem Lett 16: 2173-6 (2006) Article DOI: 10.1016/j.bmcl.2006.01.053 BindingDB Entry DOI: 10.7270/Q2319VGX
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