Compile Data Set for Download or QSAR

Found 1 hit Enz. Inhib. hit(s) with Target = 'Focal adhesion kinase 1' and Ligand = 'BDBM50184029'   

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))	BDBM50184029 (CHEMBL380424 | N-(3-hydroxypropyl)-3-(2-(3,4,5-tri...) Show SMILES COc1cc(Nc2ncc3ccn(-c4cccc(c4)C(=O)NCCCO)c3n2)cc(OC)c1OC Show InChI InChI=1S/C25H27N5O5/c1-33-20-13-18(14-21(34-2)22(20)35-3)28-25-27-15-17-8-10-30(23(17)29-25)19-7-4-6-16(12-19)24(32)26-9-5-11-31/h4,6-8,10,12-15,31H,5,9,11H2,1-3H3,(H,26,32)(H,27,28,29)	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	882	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 Inhibition of FAK				Bioorg Med Chem Lett 16: 2689-92 (2006) Article DOI: 10.1016/j.bmcl.2006.02.032 BindingDB Entry DOI: 10.7270/Q2NK3DN0
					More data for this Ligand-Target Pair