Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Kappa-type opioid receptor' and Ligand = 'BDBM50271540'   

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 (Cavia porcellus (domestic guinea pig))	BDBM50271540 ((3R,6S)-3,6-Dicyclohexyl-7-(3-cyclohexyl-propyl)-2...) Show SMILES C(CC1CCCCC1)CN1[C@H](CN2[C@@H](C[NH+]=C12)C1CCCCC1)C1CCCCC1 |r,t:16| Show InChI InChI=1S/C26H45N3/c1-4-11-21(12-5-1)13-10-18-28-25(23-16-8-3-9-17-23)20-29-24(19-27-26(28)29)22-14-6-2-7-15-22/h21-25H,1-20H2/p+1/t24-,25+/m0/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]U69593 from kappa opioid receptor in guinea pig brain homogenate				Bioorg Med Chem 16: 5932-8 (2008) Article DOI: 10.1016/j.bmc.2008.04.061 BindingDB Entry DOI: 10.7270/Q2BG2PW7
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50271540 ((3R,6S)-3,6-Dicyclohexyl-7-(3-cyclohexyl-propyl)-2...) Show SMILES C(CC1CCCCC1)CN1[C@H](CN2[C@@H](C[NH+]=C12)C1CCCCC1)C1CCCCC1 |r,t:16| Show InChI InChI=1S/C26H45N3/c1-4-11-21(12-5-1)13-10-18-28-25(23-16-8-3-9-17-23)20-29-24(19-27-26(28)29)22-14-6-2-7-15-22/h21-25H,1-20H2/p+1/t24-,25+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Inhibitory activity for kappa opioid receptor				J Med Chem 42: 3743-78 (1999) BindingDB Entry DOI: 10.7270/Q22Z167W
					More data for this Ligand-Target Pair