null

SMILES: O=C(Cc1cccc2sccc12)O[C@@H]1CCCC[C@H]1N1CCCC1

InChI Key: InChIKey=JWVVPTYSQPJIFV-QZTJIDSGSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50017492   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/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))	BDBM50017492 (Benzo[b]thiophen-4-yl-acetic acid 2-pyrrolidin-1-y...) Show SMILES O=C(Cc1cccc2sccc12)O[C@@H]1CCCC[C@H]1N1CCCC1 Show InChI InChI=1S/C20H25NO2S/c22-20(14-15-6-5-9-19-16(15)10-13-24-19)23-18-8-2-1-7-17(18)21-11-3-4-12-21/h5-6,9-10,13,17-18H,1-4,7-8,11-12,14H2/t17-,18-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	261	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Parke-Davis Research Unit Curated by ChEMBL					Assay Description Binding affinity towards opioid receptor kappa was determined				J Med Chem 32: 1620-6 (1989) BindingDB Entry DOI: 10.7270/Q2GH9JJB
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50017492 (Benzo[b]thiophen-4-yl-acetic acid 2-pyrrolidin-1-y...) Show SMILES O=C(Cc1cccc2sccc12)O[C@@H]1CCCC[C@H]1N1CCCC1 Show InChI InChI=1S/C20H25NO2S/c22-20(14-15-6-5-9-19-16(15)10-13-24-19)23-18-8-2-1-7-17(18)21-11-3-4-12-21/h5-6,9-10,13,17-18H,1-4,7-8,11-12,14H2/t17-,18-/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	3.34E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Parke-Davis Research Unit Curated by ChEMBL					Assay Description Binding affinity towards opioid receptor mu was determined				J Med Chem 32: 1620-6 (1989) BindingDB Entry DOI: 10.7270/Q2GH9JJB
					More data for this Ligand-Target Pair