null

SMILES: CN1CCC2(CC1C(=Cc1ccc3ccccc3c1)C(=O)C2)c1cccc(O)c1

InChI Key: InChIKey=ONTJNYPJIFDYJB-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50029789   

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
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM50029789 (5-(3-Hydroxy-phenyl)-2-methyl-8-[1-naphthalen-2-yl...) Show SMILES CN1CCC2(CC1C(=Cc1ccc3ccccc3c1)C(=O)C2)c1cccc(O)c1 |w:8.9| Show InChI InChI=1S/C26H25NO2/c1-27-12-11-26(21-7-4-8-22(28)15-21)16-24(27)23(25(29)17-26)14-18-9-10-19-5-2-3-6-20(19)13-18/h2-10,13-15,24,28H,11-12,16-17H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	2.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes and Digestive and Kidney Diseases Curated by ChEMBL					Assay Description Ability to inhibit [3H]-DAMGO binding to rat brain Opioid receptor mu 1				J Med Chem 38: 4776-85 (1996) BindingDB Entry DOI: 10.7270/Q2XW4HVW
					More data for this Ligand-Target Pair
Sigma non-opioid intracellular receptor 1 (Homo sapiens (Human))	BDBM50029789 (5-(3-Hydroxy-phenyl)-2-methyl-8-[1-naphthalen-2-yl...) Show SMILES CN1CCC2(CC1C(=Cc1ccc3ccccc3c1)C(=O)C2)c1cccc(O)c1 |w:8.9| Show InChI InChI=1S/C26H25NO2/c1-27-12-11-26(21-7-4-8-22(28)15-21)16-24(27)23(25(29)17-26)14-18-9-10-19-5-2-3-6-20(19)13-18/h2-10,13-15,24,28H,11-12,16-17H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	16.6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes and Digestive and Kidney Diseases Curated by ChEMBL					Assay Description Ability to inhibit [3H]-(+)-pentazocine binding to guinea pig brain Sigma receptor type 1				J Med Chem 38: 4776-85 (1996) BindingDB Entry DOI: 10.7270/Q2XW4HVW
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Rattus norvegicus (rat))	BDBM50029789 (5-(3-Hydroxy-phenyl)-2-methyl-8-[1-naphthalen-2-yl...) Show SMILES CN1CCC2(CC1C(=Cc1ccc3ccccc3c1)C(=O)C2)c1cccc(O)c1 |w:8.9| Show InChI InChI=1S/C26H25NO2/c1-27-12-11-26(21-7-4-8-22(28)15-21)16-24(27)23(25(29)17-26)14-18-9-10-19-5-2-3-6-20(19)13-18/h2-10,13-15,24,28H,11-12,16-17H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	142	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes and Digestive and Kidney Diseases Curated by ChEMBL					Assay Description Ability to inhibit [3H]-DADLE binding to rat brain delta receptor				J Med Chem 38: 4776-85 (1996) BindingDB Entry DOI: 10.7270/Q2XW4HVW
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig))	BDBM50029789 (5-(3-Hydroxy-phenyl)-2-methyl-8-[1-naphthalen-2-yl...) Show SMILES CN1CCC2(CC1C(=Cc1ccc3ccccc3c1)C(=O)C2)c1cccc(O)c1 |w:8.9| Show InChI InChI=1S/C26H25NO2/c1-27-12-11-26(21-7-4-8-22(28)15-21)16-24(27)23(25(29)17-26)14-18-9-10-19-5-2-3-6-20(19)13-18/h2-10,13-15,24,28H,11-12,16-17H2,1H3	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	>500	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes and Digestive and Kidney Diseases Curated by ChEMBL					Assay Description Ability to inhibit [3H]-U69,593 binding to guinea pig Opioid receptor kappa 1				J Med Chem 38: 4776-85 (1996) BindingDB Entry DOI: 10.7270/Q2XW4HVW
					More data for this Ligand-Target Pair