BDBM50430606 CHEMBL2338714::Isopentyl Orvinol M320

SMILES: CO[C@]12C=C[C@@]3(C[C@@H]1[C@](C)(O)CCC(C)C)[C@H]1Cc4ccc(O)c5O[C@@H]2[C@]3(CCN1CC1CC1)c45

InChI Key: InChIKey=MFIWLPVODKSMKX-XELDOGJXSA-N

Data: 2 KI  2 EC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50430606   

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))	BDBM50430606 (CHEMBL2338714 | Isopentyl Orvinol M320) Show SMILES CO[C@]12C=C[C@@]3(C[C@@H]1[C@](C)(O)CCC(C)C)[C@H]1Cc4ccc(O)c5O[C@@H]2[C@]3(CCN1CC1CC1)c45 |r,wU:8.9,5.5,16.32,wD:8.10,26.38,25.25,7.8,2.1,c:3,THB:8:7:26.25:4.3,(43.61,-49.36,;42.29,-48.59,;42.3,-47.05,;40.92,-46.19,;41.8,-45.37,;40.79,-44.38,;42.31,-44.38,;43.08,-45.72,;44.62,-45.72,;44.61,-44.16,;45.96,-44.94,;45.4,-47.07,;44.61,-48.42,;45.39,-49.77,;44.61,-51.11,;46.94,-49.77,;39.97,-43.06,;38.47,-43.06,;37.73,-44.38,;36.19,-44.38,;35.41,-45.71,;36.19,-47.02,;35.39,-48.38,;37.73,-47.02,;39.17,-47.94,;40.76,-47.02,;40,-45.71,;39.22,-44.38,;39.22,-42.49,;40,-41.52,;40.78,-40.17,;42.33,-40.14,;43.68,-40.89,;43.66,-39.34,;38.47,-45.71,)| Show InChI InChI=1S/C30H41NO4/c1-18(2)9-10-27(3,33)22-16-28-11-12-30(22,34-4)26-29(28)13-14-31(17-19-5-6-19)23(28)15-20-7-8-21(32)25(35-26)24(20)29/h7-8,11-12,18-19,22-23,26,32-33H,5-6,9-10,13-17H2,1-4H3/t22-,23-,26-,27-,28-,29+,30-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	0.0820	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bath Curated by ChEMBL					Assay Description Displacement of [3H]-diprenorphine from human KOR expressed in CHO cells				J Med Chem 56: 3207-16 (2013) Article DOI: 10.1021/jm301543e BindingDB Entry DOI: 10.7270/Q28G8N2Q
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM50430606 (CHEMBL2338714 | Isopentyl Orvinol M320) Show SMILES CO[C@]12C=C[C@@]3(C[C@@H]1[C@](C)(O)CCC(C)C)[C@H]1Cc4ccc(O)c5O[C@@H]2[C@]3(CCN1CC1CC1)c45 |r,wU:8.9,5.5,16.32,wD:8.10,26.38,25.25,7.8,2.1,c:3,THB:8:7:26.25:4.3,(43.61,-49.36,;42.29,-48.59,;42.3,-47.05,;40.92,-46.19,;41.8,-45.37,;40.79,-44.38,;42.31,-44.38,;43.08,-45.72,;44.62,-45.72,;44.61,-44.16,;45.96,-44.94,;45.4,-47.07,;44.61,-48.42,;45.39,-49.77,;44.61,-51.11,;46.94,-49.77,;39.97,-43.06,;38.47,-43.06,;37.73,-44.38,;36.19,-44.38,;35.41,-45.71,;36.19,-47.02,;35.39,-48.38,;37.73,-47.02,;39.17,-47.94,;40.76,-47.02,;40,-45.71,;39.22,-44.38,;39.22,-42.49,;40,-41.52,;40.78,-40.17,;42.33,-40.14,;43.68,-40.89,;43.66,-39.34,;38.47,-45.71,)| Show InChI InChI=1S/C30H41NO4/c1-18(2)9-10-27(3,33)22-16-28-11-12-30(22,34-4)26-29(28)13-14-31(17-19-5-6-19)23(28)15-20-7-8-21(32)25(35-26)24(20)29/h7-8,11-12,18-19,22-23,26,32-33H,5-6,9-10,13-17H2,1-4H3/t22-,23-,26-,27-,28-,29+,30-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	0.180	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Bath Curated by ChEMBL					Assay Description Displacement of [3H]-diprenorphine from rat recombinant MOR expressed in rat C6 cells after 2 hrs				J Med Chem 56: 3207-16 (2013) Article DOI: 10.1021/jm301543e BindingDB Entry DOI: 10.7270/Q28G8N2Q
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM50430606 (CHEMBL2338714 | Isopentyl Orvinol M320) Show SMILES CO[C@]12C=C[C@@]3(C[C@@H]1[C@](C)(O)CCC(C)C)[C@H]1Cc4ccc(O)c5O[C@@H]2[C@]3(CCN1CC1CC1)c45 |r,wU:8.9,5.5,16.32,wD:8.10,26.38,25.25,7.8,2.1,c:3,THB:8:7:26.25:4.3,(43.61,-49.36,;42.29,-48.59,;42.3,-47.05,;40.92,-46.19,;41.8,-45.37,;40.79,-44.38,;42.31,-44.38,;43.08,-45.72,;44.62,-45.72,;44.61,-44.16,;45.96,-44.94,;45.4,-47.07,;44.61,-48.42,;45.39,-49.77,;44.61,-51.11,;46.94,-49.77,;39.97,-43.06,;38.47,-43.06,;37.73,-44.38,;36.19,-44.38,;35.41,-45.71,;36.19,-47.02,;35.39,-48.38,;37.73,-47.02,;39.17,-47.94,;40.76,-47.02,;40,-45.71,;39.22,-44.38,;39.22,-42.49,;40,-41.52,;40.78,-40.17,;42.33,-40.14,;43.68,-40.89,;43.66,-39.34,;38.47,-45.71,)| Show InChI InChI=1S/C30H41NO4/c1-18(2)9-10-27(3,33)22-16-28-11-12-30(22,34-4)26-29(28)13-14-31(17-19-5-6-19)23(28)15-20-7-8-21(32)25(35-26)24(20)29/h7-8,11-12,18-19,22-23,26,32-33H,5-6,9-10,13-17H2,1-4H3/t22-,23-,26-,27-,28-,29+,30-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	1	n/a	n/a	n/a	n/a
University of Bath Curated by ChEMBL					Assay Description Agonist activity at rat recombinant MOR expressed in rat C6 cells assessed as stimulation of [35S]GTPgammaS binding after 1 hr				J Med Chem 56: 3207-16 (2013) Article DOI: 10.1021/jm301543e BindingDB Entry DOI: 10.7270/Q28G8N2Q
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50430606 (CHEMBL2338714 | Isopentyl Orvinol M320) Show SMILES CO[C@]12C=C[C@@]3(C[C@@H]1[C@](C)(O)CCC(C)C)[C@H]1Cc4ccc(O)c5O[C@@H]2[C@]3(CCN1CC1CC1)c45 |r,wU:8.9,5.5,16.32,wD:8.10,26.38,25.25,7.8,2.1,c:3,THB:8:7:26.25:4.3,(43.61,-49.36,;42.29,-48.59,;42.3,-47.05,;40.92,-46.19,;41.8,-45.37,;40.79,-44.38,;42.31,-44.38,;43.08,-45.72,;44.62,-45.72,;44.61,-44.16,;45.96,-44.94,;45.4,-47.07,;44.61,-48.42,;45.39,-49.77,;44.61,-51.11,;46.94,-49.77,;39.97,-43.06,;38.47,-43.06,;37.73,-44.38,;36.19,-44.38,;35.41,-45.71,;36.19,-47.02,;35.39,-48.38,;37.73,-47.02,;39.17,-47.94,;40.76,-47.02,;40,-45.71,;39.22,-44.38,;39.22,-42.49,;40,-41.52,;40.78,-40.17,;42.33,-40.14,;43.68,-40.89,;43.66,-39.34,;38.47,-45.71,)| Show InChI InChI=1S/C30H41NO4/c1-18(2)9-10-27(3,33)22-16-28-11-12-30(22,34-4)26-29(28)13-14-31(17-19-5-6-19)23(28)15-20-7-8-21(32)25(35-26)24(20)29/h7-8,11-12,18-19,22-23,26,32-33H,5-6,9-10,13-17H2,1-4H3/t22-,23-,26-,27-,28-,29+,30-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	0.0510	n/a	n/a	n/a	n/a
University of Bath Curated by ChEMBL					Assay Description Agonist activity at human KOR expressed in CHO cells assessed as stimulation of [35S]GTPgammaS binding				J Med Chem 56: 3207-16 (2013) Article DOI: 10.1021/jm301543e BindingDB Entry DOI: 10.7270/Q28G8N2Q
					More data for this Ligand-Target Pair