Compile Data Set for Download or QSAR

Found 1 hit Enz. Inhib. hit(s) with Target = 'Focal adhesion kinase 1' and Ligand = 'BDBM50182002'   

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))	BDBM50182002 (4-methyl-3-(7-(pyridin-2-yl)-7H-pyrrolo[2,3-d]pyri...) Show SMILES Cc1ccc(cc1Nc1ncc2ccn(-c3ccccn3)c2n1)C(N)=O Show InChI InChI=1S/C19H16N6O/c1-12-5-6-13(17(20)26)10-15(12)23-19-22-11-14-7-9-25(18(14)24-19)16-4-2-3-8-21-16/h2-11H,1H3,(H2,20,26)(H,22,23,24)	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	400	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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