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SMILES: COc1ccc(CN2CC[C@](C)([C@@H](C)C2)c2cccc(c2)C(N)=O)cc1

InChI Key: InChIKey=HSNRGCAFLLPJJV-KSFYIVLOSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50136598   

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))	BDBM50136598 (3-[(3R,4R)-1-(4-Methoxy-benzyl)-3,4-dimethyl-piper...) Show SMILES COc1ccc(CN2CC[C@](C)([C@@H](C)C2)c2cccc(c2)C(N)=O)cc1 Show InChI InChI=1S/C22H28N2O2/c1-16-14-24(15-17-7-9-20(26-3)10-8-17)12-11-22(16,2)19-6-4-5-18(13-19)21(23)25/h4-10,13,16H,11-12,14-15H2,1-3H3,(H2,23,25)/t16-,22+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	5.5	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 binding of the non-selective opioid antagonist, [3H]diprenorphine, to cloned human mu opioid receptor				Bioorg Med Chem Lett 13: 4459-62 (2003) BindingDB Entry DOI: 10.7270/Q2RV0P7G
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50136598 (3-[(3R,4R)-1-(4-Methoxy-benzyl)-3,4-dimethyl-piper...) Show SMILES COc1ccc(CN2CC[C@](C)([C@@H](C)C2)c2cccc(c2)C(N)=O)cc1 Show InChI InChI=1S/C22H28N2O2/c1-16-14-24(15-17-7-9-20(26-3)10-8-17)12-11-22(16,2)19-6-4-5-18(13-19)21(23)25/h4-10,13,16H,11-12,14-15H2,1-3H3,(H2,23,25)/t16-,22+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	220	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Adolor Corporation Curated by ChEMBL					Assay Description Binding affinity at cloned human kappa opioid receptor by [3H]diprenorphine displacement.				Bioorg Med Chem Lett 13: 4459-62 (2003) BindingDB Entry DOI: 10.7270/Q2RV0P7G
					More data for this Ligand-Target Pair