Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Cholecystokinin receptor type A' and Ligand = 'BDBM50262971'   

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
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50262971 ((4-(naphthalen-2-yl)piperazin-1-yl)(2-p-tolyl-1-(3...) Show SMILES Cc1ccc(cc1)-c1nc(cn1-c1cccc(OC(F)(F)F)c1)C(=O)N1CCN(CC1)c1ccc2ccccc2c1 Show InChI InChI=1S/C32H27F3N4O2/c1-22-9-11-24(12-10-22)30-36-29(21-39(30)27-7-4-8-28(20-27)41-32(33,34)35)31(40)38-17-15-37(16-18-38)26-14-13-23-5-2-3-6-25(23)19-26/h2-14,19-21H,15-18H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	130	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibition of human CCK1 receptor				Bioorg Med Chem Lett 18: 4393-6 (2008) Article DOI: 10.1016/j.bmcl.2008.06.057 BindingDB Entry DOI: 10.7270/Q2HH6JW0
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (Homo sapiens (Human))	BDBM50262971 ((4-(naphthalen-2-yl)piperazin-1-yl)(2-p-tolyl-1-(3...) Show SMILES Cc1ccc(cc1)-c1nc(cn1-c1cccc(OC(F)(F)F)c1)C(=O)N1CCN(CC1)c1ccc2ccccc2c1 Show InChI InChI=1S/C32H27F3N4O2/c1-22-9-11-24(12-10-22)30-36-29(21-39(30)27-7-4-8-28(20-27)41-32(33,34)35)31(40)38-17-15-37(16-18-38)26-14-13-23-5-2-3-6-25(23)19-26/h2-14,19-21H,15-18H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	3.15E+3	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Agonist activity against human CCK1 receptor				Bioorg Med Chem Lett 18: 4393-6 (2008) Article DOI: 10.1016/j.bmcl.2008.06.057 BindingDB Entry DOI: 10.7270/Q2HH6JW0
					More data for this Ligand-Target Pair