Compile Data Set for Download or QSAR

Found 3 hits Enz. Inhib. hit(s) with Target = 'Kappa-type opioid receptor' and Ligand = 'BDBM50266445'   

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
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50266445 ((2S,4aR,6aR,7R,9S,10aS,10bR)-2-isopropyl 7-methyl ...) Show SMILES COC(=O)[C@@H]1C[C@H](OC(C)=O)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@@H](C[C@]21C)C(=O)OC(C)C |r| Show InChI InChI=1S/C23H32O9/c1-11(2)30-21(28)16-10-23(5)13(20(27)32-16)7-8-22(4)14(19(26)29-6)9-15(31-12(3)24)17(25)18(22)23/h11,13-16,18H,7-10H2,1-6H3/t13-,14-,15-,16-,18-,22-,23-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	US Patent	109	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The McLean Hospital Corporation; Temple University School of Medicine US Patent					Assay Description In vitro binding assay: The affinities of compounds for opioid receptors were determined by competitive inhibition of [3H]diprenorphine binding to ka...				US Patent US8492564 (2013) BindingDB Entry DOI: 10.7270/Q2NV9GW0
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50266445 ((2S,4aR,6aR,7R,9S,10aS,10bR)-2-isopropyl 7-methyl ...) Show SMILES COC(=O)[C@@H]1C[C@H](OC(C)=O)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@@H](C[C@]21C)C(=O)OC(C)C |r| Show InChI InChI=1S/C23H32O9/c1-11(2)30-21(28)16-10-23(5)13(20(27)32-16)7-8-22(4)14(19(26)29-6)9-15(31-12(3)24)17(25)18(22)23/h11,13-16,18H,7-10H2,1-6H3/t13-,14-,15-,16-,18-,22-,23-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	109	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
McLean Hospital Curated by ChEMBL					Assay Description Displacement of [3H]diprenorphine from human KOPR expressed in CHO cells				Bioorg Med Chem 17: 1370-80 (2009) Article DOI: 10.1016/j.bmc.2008.12.012 BindingDB Entry DOI: 10.7270/Q25H7G4K
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50266445 ((2S,4aR,6aR,7R,9S,10aS,10bR)-2-isopropyl 7-methyl ...) Show SMILES COC(=O)[C@@H]1C[C@H](OC(C)=O)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@@H](C[C@]21C)C(=O)OC(C)C |r| Show InChI InChI=1S/C23H32O9/c1-11(2)30-21(28)16-10-23(5)13(20(27)32-16)7-8-22(4)14(19(26)29-6)9-15(31-12(3)24)17(25)18(22)23/h11,13-16,18H,7-10H2,1-6H3/t13-,14-,15-,16-,18-,22-,23-/m0/s1	PDB 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	n/a	n/a	337	n/a	n/a	n/a	n/a
McLean Hospital Curated by ChEMBL					Assay Description Agonist activity at human KOPR expressed in CHO cells assessed as enhancenment of [35S]GTPgammaS binding				Bioorg Med Chem 17: 1370-80 (2009) Article DOI: 10.1016/j.bmc.2008.12.012 BindingDB Entry DOI: 10.7270/Q25H7G4K
					More data for this Ligand-Target Pair