BDBM50386663 CHEMBL2048761

SMILES: COc1cccc(CNc2ccc3C[C@@H]4[C@@H]5CCCC[C@]5(CCN4CC4CCC4)c3c2)c1

InChI Key: InChIKey=ZPCWMLZBHFMKBB-WIIGKZCBSA-N

Data: 3 KI  1 IC50  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 6 hits for monomerid = 50386663   

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 (Homo sapiens (Human))	BDBM50386663 (CHEMBL2048761) Show SMILES COc1cccc(CNc2ccc3C[C@@H]4[C@@H]5CCCC[C@]5(CCN4CC4CCC4)c3c2)c1 |r| Show InChI InChI=1S/C29H38N2O/c1-32-25-9-5-8-22(16-25)19-30-24-12-11-23-17-28-26-10-2-3-13-29(26,27(23)18-24)14-15-31(28)20-21-6-4-7-21/h5,8-9,11-12,16,18,21,26,28,30H,2-4,6-7,10,13-15,17,19-20H2,1H3/t26-,28+,29+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	0.690	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Harvard Medical School Curated by ChEMBL					Assay Description Displacement of [3H]-DAMGO from human mu opioid receptor expressed in CHO cells after 60 mins by scintillation counting				J Med Chem 55: 3878-90 (2012) Article DOI: 10.1021/jm3001086 BindingDB Entry DOI: 10.7270/Q28053P6
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50386663 (CHEMBL2048761) Show SMILES COc1cccc(CNc2ccc3C[C@@H]4[C@@H]5CCCC[C@]5(CCN4CC4CCC4)c3c2)c1 |r| Show InChI InChI=1S/C29H38N2O/c1-32-25-9-5-8-22(16-25)19-30-24-12-11-23-17-28-26-10-2-3-13-29(26,27(23)18-24)14-15-31(28)20-21-6-4-7-21/h5,8-9,11-12,16,18,21,26,28,30H,2-4,6-7,10,13-15,17,19-20H2,1H3/t26-,28+,29+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Harvard Medical School Curated by ChEMBL					Assay Description Displacement of [3H]-U69,593 from human kappa opioid receptor expressed in CHO cells after 60 mins by scintillation counting				J Med Chem 55: 3878-90 (2012) Article DOI: 10.1021/jm3001086 BindingDB Entry DOI: 10.7270/Q28053P6
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50386663 (CHEMBL2048761) Show SMILES COc1cccc(CNc2ccc3C[C@@H]4[C@@H]5CCCC[C@]5(CCN4CC4CCC4)c3c2)c1 |r| Show InChI InChI=1S/C29H38N2O/c1-32-25-9-5-8-22(16-25)19-30-24-12-11-23-17-28-26-10-2-3-13-29(26,27(23)18-24)14-15-31(28)20-21-6-4-7-21/h5,8-9,11-12,16,18,21,26,28,30H,2-4,6-7,10,13-15,17,19-20H2,1H3/t26-,28+,29+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	150	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Harvard Medical School Curated by ChEMBL					Assay Description Displacement of [3H]-naltrindole from human delta opioid receptor expressed in CHO cells after 3 hrs by scintillation counting				J Med Chem 55: 3878-90 (2012) Article DOI: 10.1021/jm3001086 BindingDB Entry DOI: 10.7270/Q28053P6
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50386663 (CHEMBL2048761) Show SMILES COc1cccc(CNc2ccc3C[C@@H]4[C@@H]5CCCC[C@]5(CCN4CC4CCC4)c3c2)c1 |r| Show InChI InChI=1S/C29H38N2O/c1-32-25-9-5-8-22(16-25)19-30-24-12-11-23-17-28-26-10-2-3-13-29(26,27(23)18-24)14-15-31(28)20-21-6-4-7-21/h5,8-9,11-12,16,18,21,26,28,30H,2-4,6-7,10,13-15,17,19-20H2,1H3/t26-,28+,29+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	80	n/a	n/a	n/a	n/a	n/a	n/a
Harvard Medical School Curated by ChEMBL					Assay Description Antagonist activity at human mu opioid receptor expressed in CHO cells assessed as inhibition of DAMGO-induced [33S]GTPgammaS binding after 60 mins b...				J Med Chem 55: 3878-90 (2012) Article DOI: 10.1021/jm3001086 BindingDB Entry DOI: 10.7270/Q28053P6
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50386663 (CHEMBL2048761) Show SMILES COc1cccc(CNc2ccc3C[C@@H]4[C@@H]5CCCC[C@]5(CCN4CC4CCC4)c3c2)c1 |r| Show InChI InChI=1S/C29H38N2O/c1-32-25-9-5-8-22(16-25)19-30-24-12-11-23-17-28-26-10-2-3-13-29(26,27(23)18-24)14-15-31(28)20-21-6-4-7-21/h5,8-9,11-12,16,18,21,26,28,30H,2-4,6-7,10,13-15,17,19-20H2,1H3/t26-,28+,29+/m0/s1	PDB NCI pathway 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	3.80	n/a	n/a	n/a	n/a
Harvard Medical School Curated by ChEMBL					Assay Description Agonist activity at human mu opioid receptor expressed in CHO cells assessed as stimulation of [33S]GTPgammaS binding after 60 mins by scintillation ...				J Med Chem 55: 3878-90 (2012) Article DOI: 10.1021/jm3001086 BindingDB Entry DOI: 10.7270/Q28053P6
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50386663 (CHEMBL2048761) Show SMILES COc1cccc(CNc2ccc3C[C@@H]4[C@@H]5CCCC[C@]5(CCN4CC4CCC4)c3c2)c1 |r| Show InChI InChI=1S/C29H38N2O/c1-32-25-9-5-8-22(16-25)19-30-24-12-11-23-17-28-26-10-2-3-13-29(26,27(23)18-24)14-15-31(28)20-21-6-4-7-21/h5,8-9,11-12,16,18,21,26,28,30H,2-4,6-7,10,13-15,17,19-20H2,1H3/t26-,28+,29+/m0/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	39	n/a	n/a	n/a	n/a
Harvard Medical School Curated by ChEMBL					Assay Description Agonist activity at human kappa opioid receptor expressed in CHO cells assessed as stimulation of [33S]GTPgammaS binding after 60 mins by scintillati...				J Med Chem 55: 3878-90 (2012) Article DOI: 10.1021/jm3001086 BindingDB Entry DOI: 10.7270/Q28053P6
					More data for this Ligand-Target Pair