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SMILES: O=S1(=O)Nc2ccccc2N1C1CCN(CC1)C1CCCCCCC1

InChI Key: InChIKey=STJLVIZIMKQOFN-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50153146   

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
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50153146 (1-(1-Cyclooctyl-piperidin-4-yl)-1,3-dihydro-benzo[...) Show SMILES O=S1(=O)Nc2ccccc2N1C1CCN(CC1)C1CCCCCCC1 Show InChI InChI=1S/C19H29N3O2S/c23-25(24)20-18-10-6-7-11-19(18)22(25)17-12-14-21(15-13-17)16-8-4-2-1-3-5-9-16/h6-7,10-11,16-17,20H,1-5,8-9,12-15H2	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Purdue Pharma LP Curated by ChEMBL					Assay Description Inhibition of [3H]naltrindole binding to human Opioid receptor delta 1				Bioorg Med Chem Lett 14: 5045-50 (2004) Article DOI: 10.1016/j.bmcl.2004.08.001 BindingDB Entry DOI: 10.7270/Q2TM7BV8
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50153146 (1-(1-Cyclooctyl-piperidin-4-yl)-1,3-dihydro-benzo[...) Show SMILES O=S1(=O)Nc2ccccc2N1C1CCN(CC1)C1CCCCCCC1 Show InChI InChI=1S/C19H29N3O2S/c23-25(24)20-18-10-6-7-11-19(18)22(25)17-12-14-21(15-13-17)16-8-4-2-1-3-5-9-16/h6-7,10-11,16-17,20H,1-5,8-9,12-15H2	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Purdue Pharma LP Curated by ChEMBL					Assay Description Inhibition of [3H]U-69593 binding to human Opioid receptor kappa 1				Bioorg Med Chem Lett 14: 5045-50 (2004) Article DOI: 10.1016/j.bmcl.2004.08.001 BindingDB Entry DOI: 10.7270/Q2TM7BV8
					More data for this Ligand-Target Pair
Nociceptin receptor (Homo sapiens (Human))	BDBM50153146 (1-(1-Cyclooctyl-piperidin-4-yl)-1,3-dihydro-benzo[...) Show SMILES O=S1(=O)Nc2ccccc2N1C1CCN(CC1)C1CCCCCCC1 Show InChI InChI=1S/C19H29N3O2S/c23-25(24)20-18-10-6-7-11-19(18)22(25)17-12-14-21(15-13-17)16-8-4-2-1-3-5-9-16/h6-7,10-11,16-17,20H,1-5,8-9,12-15H2	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Purdue Pharma LP Curated by ChEMBL					Assay Description Agonist activity as stimulation of [35S]-GTP-gamma binding to human Opioid receptor like 1				Bioorg Med Chem Lett 14: 5045-50 (2004) Article DOI: 10.1016/j.bmcl.2004.08.001 BindingDB Entry DOI: 10.7270/Q2TM7BV8
					More data for this Ligand-Target Pair