Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Kappa-type opioid receptor' and Ligand = 'BDBM50148910'   

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))	BDBM50148910 (CHEMBL3770668) Show SMILES Cc1cc(O)ccc1C[C@H](N)C(=O)N[C@@H]1CCNc2ccc(Cc3ccccc3)cc12 |r| Show InChI InChI=1S/C26H29N3O2/c1-17-13-21(30)9-8-20(17)16-23(27)26(31)29-25-11-12-28-24-10-7-19(15-22(24)25)14-18-5-3-2-4-6-18/h2-10,13,15,23,25,28,30H,11-12,14,16,27H2,1H3,(H,29,31)/t23-,25+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	96	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Michigan Curated by ChEMBL					Assay Description Displacement of [3H]diprenorphine from human KOR expressed in CHO cells after 1 hr by liquid scintillation counting method				ACS Med Chem Lett 6: 1199-203 (2015) Article DOI: 10.1021/acsmedchemlett.5b00344 BindingDB Entry DOI: 10.7270/Q20V8FN5
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50148910 (CHEMBL3770668) Show SMILES Cc1cc(O)ccc1C[C@H](N)C(=O)N[C@@H]1CCNc2ccc(Cc3ccccc3)cc12 |r| Show InChI InChI=1S/C26H29N3O2/c1-17-13-21(30)9-8-20(17)16-23(27)26(31)29-25-11-12-28-24-10-7-19(15-22(24)25)14-18-5-3-2-4-6-18/h2-10,13,15,23,25,28,30H,11-12,14,16,27H2,1H3,(H,29,31)/t23-,25+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	2.40E+3	n/a	n/a	n/a	n/a
University of Michigan Curated by ChEMBL					Assay Description Agonist activity at human KOR expressed in CHO cells after 1 hr by [35S]GTPgammaS binding assay				ACS Med Chem Lett 6: 1199-203 (2015) Article DOI: 10.1021/acsmedchemlett.5b00344 BindingDB Entry DOI: 10.7270/Q20V8FN5
					More data for this Ligand-Target Pair