null

SMILES: C[C@H]1CN(CCc2ccccc2)[C@H](CCNC(=O)c2ccccc2)C[C@@]1(C)c1cccc(O)c1

InChI Key: InChIKey=LNEHCLOLWAQHIF-NTGKZJMKSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50177685   

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))	BDBM50177685 (CHEMBL201845 | N-(2-(4-(3-hydroxyphenyl)-trans-4,5...) Show SMILES C[C@H]1CN(CCc2ccccc2)[C@H](CCNC(=O)c2ccccc2)C[C@@]1(C)c1cccc(O)c1 Show InChI InChI=1S/C30H36N2O2/c1-23-22-32(19-17-24-10-5-3-6-11-24)27(16-18-31-29(34)25-12-7-4-8-13-25)21-30(23,2)26-14-9-15-28(33)20-26/h3-15,20,23,27,33H,16-19,21-22H2,1-2H3,(H,31,34)/t23-,27+,30+/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	59	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Adolor Corporation Curated by ChEMBL					Assay Description Inhibition of loperamide-stimulated [35S]GTP-gamma-S binding to membranes containing mu opioid receptor				Bioorg Med Chem Lett 16: 864-8 (2006) Article DOI: 10.1016/j.bmcl.2005.11.010 BindingDB Entry DOI: 10.7270/Q2RJ4J1J
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50177685 (CHEMBL201845 | N-(2-(4-(3-hydroxyphenyl)-trans-4,5...) Show SMILES C[C@H]1CN(CCc2ccccc2)[C@H](CCNC(=O)c2ccccc2)C[C@@]1(C)c1cccc(O)c1 Show InChI InChI=1S/C30H36N2O2/c1-23-22-32(19-17-24-10-5-3-6-11-24)27(16-18-31-29(34)25-12-7-4-8-13-25)21-30(23,2)26-14-9-15-28(33)20-26/h3-15,20,23,27,33H,16-19,21-22H2,1-2H3,(H,31,34)/t23-,27+,30+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	200	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Adolor Corporation Curated by ChEMBL					Assay Description Displacement of [3H]diprenorphine from human cloned kappa opioid receptor				Bioorg Med Chem Lett 16: 864-8 (2006) Article DOI: 10.1016/j.bmcl.2005.11.010 BindingDB Entry DOI: 10.7270/Q2RJ4J1J
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50177685 (CHEMBL201845 | N-(2-(4-(3-hydroxyphenyl)-trans-4,5...) Show SMILES C[C@H]1CN(CCc2ccccc2)[C@H](CCNC(=O)c2ccccc2)C[C@@]1(C)c1cccc(O)c1 Show InChI InChI=1S/C30H36N2O2/c1-23-22-32(19-17-24-10-5-3-6-11-24)27(16-18-31-29(34)25-12-7-4-8-13-25)21-30(23,2)26-14-9-15-28(33)20-26/h3-15,20,23,27,33H,16-19,21-22H2,1-2H3,(H,31,34)/t23-,27+,30+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	710	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Adolor Corporation Curated by ChEMBL					Assay Description Displacement of [3H]diprenorphine from human cloned delta opioid receptor				Bioorg Med Chem Lett 16: 864-8 (2006) Article DOI: 10.1016/j.bmcl.2005.11.010 BindingDB Entry DOI: 10.7270/Q2RJ4J1J
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50177685 (CHEMBL201845 | N-(2-(4-(3-hydroxyphenyl)-trans-4,5...) Show SMILES C[C@H]1CN(CCc2ccccc2)[C@H](CCNC(=O)c2ccccc2)C[C@@]1(C)c1cccc(O)c1 Show InChI InChI=1S/C30H36N2O2/c1-23-22-32(19-17-24-10-5-3-6-11-24)27(16-18-31-29(34)25-12-7-4-8-13-25)21-30(23,2)26-14-9-15-28(33)20-26/h3-15,20,23,27,33H,16-19,21-22H2,1-2H3,(H,31,34)/t23-,27+,30+/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	130	n/a	n/a	n/a	n/a	n/a	n/a
Adolor Corporation Curated by ChEMBL					Assay Description Inhibition of loperamide-stimulated [35S]GTPgammaS binding to membranes containing mu opioid receptor				Bioorg Med Chem Lett 16: 864-8 (2006) Article DOI: 10.1016/j.bmcl.2005.11.010 BindingDB Entry DOI: 10.7270/Q2RJ4J1J
					More data for this Ligand-Target Pair