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SMILES: CN1CCC2(CC1C(=Cc1cccc(I)c1)C(=O)C2)c1cccc(O)c1

InChI Key: InChIKey=JTZKNEJWQJLWTH-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50029792   

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
Sigma non-opioid intracellular receptor 1 (Homo sapiens (Human))	BDBM50029792 (5-(3-Hydroxy-phenyl)-8-[1-(3-iodo-phenyl)-meth-(E)...) Show SMILES CN1CCC2(CC1C(=Cc1cccc(I)c1)C(=O)C2)c1cccc(O)c1 |w:8.9| Show InChI InChI=1S/C22H22INO2/c1-24-9-8-22(16-5-3-7-18(25)12-16)13-20(24)19(21(26)14-22)11-15-4-2-6-17(23)10-15/h2-7,10-12,20,25H,8-9,13-14H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.62	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
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM50029792 (5-(3-Hydroxy-phenyl)-8-[1-(3-iodo-phenyl)-meth-(E)...) Show SMILES CN1CCC2(CC1C(=Cc1cccc(I)c1)C(=O)C2)c1cccc(O)c1 |w:8.9| Show InChI InChI=1S/C22H22INO2/c1-24-9-8-22(16-5-3-7-18(25)12-16)13-20(24)19(21(26)14-22)11-15-4-2-6-17(23)10-15/h2-7,10-12,20,25H,8-9,13-14H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	9.10	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
Delta-type opioid receptor (Rattus norvegicus (rat))	BDBM50029792 (5-(3-Hydroxy-phenyl)-8-[1-(3-iodo-phenyl)-meth-(E)...) Show SMILES CN1CCC2(CC1C(=Cc1cccc(I)c1)C(=O)C2)c1cccc(O)c1 |w:8.9| Show InChI InChI=1S/C22H22INO2/c1-24-9-8-22(16-5-3-7-18(25)12-16)13-20(24)19(21(26)14-22)11-15-4-2-6-17(23)10-15/h2-7,10-12,20,25H,8-9,13-14H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	141	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))	BDBM50029792 (5-(3-Hydroxy-phenyl)-8-[1-(3-iodo-phenyl)-meth-(E)...) Show SMILES CN1CCC2(CC1C(=Cc1cccc(I)c1)C(=O)C2)c1cccc(O)c1 |w:8.9| Show InChI InChI=1S/C22H22INO2/c1-24-9-8-22(16-5-3-7-18(25)12-16)13-20(24)19(21(26)14-22)11-15-4-2-6-17(23)10-15/h2-7,10-12,20,25H,8-9,13-14H2,1H3	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