Compile Data Set for Download or QSAR

Found 3 hits Enz. Inhib. hit(s) with Target = 'Cholecystokinin receptor type A' and Ligand = 'BDBM50281711'   

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 (RAT)	BDBM50281711 (1-(4-Chloro-phenyl)-3-((R)-1-methyl-2-oxo-5-phenyl...) Show SMILES CN1c2ccccc2C(=N[C@@H](NC(=O)Nc2ccc(Cl)cc2)C1=O)c1ccccc1 |c:9| Show InChI InChI=1S/C23H19ClN4O2/c1-28-19-10-6-5-9-18(19)20(15-7-3-2-4-8-15)26-21(22(28)29)27-23(30)25-17-13-11-16(24)12-14-17/h2-14,21H,1H3,(H2,25,27,30)/t21-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Tested for its activity to inhibit the binding of [125I]-CCK-33 to Cholecystokinin type A receptor in rat pancreas				Bioorg Med Chem Lett 3: 867-870 (1993) Article DOI: 10.1016/S0960-894X(00)80682-4 BindingDB Entry DOI: 10.7270/Q28S4PTK
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (RAT)	BDBM50281711 (1-(4-Chloro-phenyl)-3-((R)-1-methyl-2-oxo-5-phenyl...) Show SMILES CN1c2ccccc2C(=N[C@@H](NC(=O)Nc2ccc(Cl)cc2)C1=O)c1ccccc1 |c:9| Show InChI InChI=1S/C23H19ClN4O2/c1-28-19-10-6-5-9-18(19)20(15-7-3-2-4-8-15)26-21(22(28)29)27-23(30)25-17-13-11-16(24)12-14-17/h2-14,21H,1H3,(H2,25,27,30)/t21-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Merck Sharp& Dohme Research Laboratories Curated by ChEMBL					Assay Description Displacement of [125 I] CCK-8 from Cholecystokinin type A receptor of rat pancreas				J Med Chem 32: 13-6 (1989) BindingDB Entry DOI: 10.7270/Q2MC90MG
					More data for this Ligand-Target Pair
Cholecystokinin receptor type A (RAT)	BDBM50281711 (1-(4-Chloro-phenyl)-3-((R)-1-methyl-2-oxo-5-phenyl...) Show SMILES CN1c2ccccc2C(=N[C@@H](NC(=O)Nc2ccc(Cl)cc2)C1=O)c1ccccc1 |c:9| Show InChI InChI=1S/C23H19ClN4O2/c1-28-19-10-6-5-9-18(19)20(15-7-3-2-4-8-15)26-21(22(28)29)27-23(30)25-17-13-11-16(24)12-14-17/h2-14,21H,1H3,(H2,25,27,30)/t21-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	2.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibition of binding of [125I]CCK-8 to cholecystokinin type A receptor in rat pancreatic tissue				J Med Chem 36: 4276-92 (1994) BindingDB Entry DOI: 10.7270/Q22J6CH9
					More data for this Ligand-Target Pair