Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Tyrosine-protein kinase Lck' and Ligand = 'BDBM13239'   

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
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM13239 (2-[[(Cyclopropyl)carbonyl]-amino]-4-methyl-N-(2-ch...) Show SMILES Cc1nc(NC(=O)C2CC2)sc1C(=O)Nc1c(C)cccc1Cl Show InChI InChI=1S/C16H16ClN3O2S/c1-8-4-3-5-11(17)12(8)19-15(22)13-9(2)18-16(23-13)20-14(21)10-6-7-10/h3-5,10H,6-7H2,1-2H3,(H,19,22)(H,18,20,21)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Pharmaceutical Research Institute Curated by ChEMBL					Assay Description Inhibitory activity of the compound human Lck(hLck) kinase				Bioorg Med Chem Lett 13: 4007-10 (2003) BindingDB Entry DOI: 10.7270/Q2CC103J
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM13239 (2-[[(Cyclopropyl)carbonyl]-amino]-4-methyl-N-(2-ch...) Show SMILES Cc1nc(NC(=O)C2CC2)sc1C(=O)Nc1c(C)cccc1Cl Show InChI InChI=1S/C16H16ClN3O2S/c1-8-4-3-5-11(17)12(8)19-15(22)13-9(2)18-16(23-13)20-14(21)10-6-7-10/h3-5,10H,6-7H2,1-2H3,(H,19,22)(H,18,20,21)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Company					Assay Description IC50 is the inhibitor concentration, which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-33P] lab...				J Med Chem 49: 6819-32 (2006) Article DOI: 10.1021/jm060727j BindingDB Entry DOI: 10.7270/Q2QN6501
					More data for this Ligand-Target Pair