Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Kappa-type opioid receptor' and Ligand = 'BDBM50027101'   

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))	BDBM50027101 (CHEMBL2113376) Show SMILES [H][C@@]12Oc3c4c(CC5N(C)CC[C@@]14[C@@]5(N)Cc1c2[nH]c2ccccc12)ccc3O |THB:9:8:13:4.5.6| Show InChI InChI=1S/C23H23N3O2/c1-26-9-8-22-18-12-6-7-16(27)20(18)28-21(22)19-14(11-23(22,24)17(26)10-12)13-4-2-3-5-15(13)25-19/h2-7,17,21,25,27H,8-11,24H2,1H3/t17?,21-,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	399	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bath Curated by ChEMBL					Assay Description Displacement of [3H]U-69593 from human recombinant Opioid receptor kappa 1 on CHO cell membranes.				J Med Chem 46: 1563-6 (2003) Article DOI: 10.1021/jm021073r BindingDB Entry DOI: 10.7270/Q27945F9
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50027101 (CHEMBL2113376) Show SMILES [H][C@@]12Oc3c4c(CC5N(C)CC[C@@]14[C@@]5(N)Cc1c2[nH]c2ccccc12)ccc3O |THB:9:8:13:4.5.6| Show InChI InChI=1S/C23H23N3O2/c1-26-9-8-22-18-12-6-7-16(27)20(18)28-21(22)19-14(11-23(22,24)17(26)10-12)13-4-2-3-5-15(13)25-19/h2-7,17,21,25,27H,8-11,24H2,1H3/t17?,21-,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	87	n/a	n/a	n/a	n/a
University of Bath Curated by ChEMBL					Assay Description Stimulation of U-69,593 binding at human recombinant Opioid receptor kappa 1 transfected into CHO cells.				J Med Chem 46: 1563-6 (2003) Article DOI: 10.1021/jm021073r BindingDB Entry DOI: 10.7270/Q27945F9
					More data for this Ligand-Target Pair