null

SMILES: CN([C@H](CN1CC[C@H](O)C1)c1ccccc1)C(=O)CC(=O)NCc1ccccc1

InChI Key: InChIKey=KSAJTKITKDZSQD-LEWJYISDSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50205679   

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))	BDBM50205679 (CHEMBL395288 | N1-benzyl-N3-((S)-2-((S)-3-hydroxyp...) Show SMILES CN([C@H](CN1CC[C@H](O)C1)c1ccccc1)C(=O)CC(=O)NCc1ccccc1 Show InChI InChI=1S/C23H29N3O3/c1-25(23(29)14-22(28)24-15-18-8-4-2-5-9-18)21(19-10-6-3-7-11-19)17-26-13-12-20(27)16-26/h2-11,20-21,27H,12-17H2,1H3,(H,24,28)/t20-,21+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	15	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Adolor Corporation Curated by ChEMBL					Assay Description Agonist activity at human kappa opioid receptor by [35S]GTPgammaS binding assay				Bioorg Med Chem Lett 17: 1951-5 (2007) Article DOI: 10.1016/j.bmcl.2007.01.053 BindingDB Entry DOI: 10.7270/Q2Q52P9X
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM50205679 (CHEMBL395288 | N1-benzyl-N3-((S)-2-((S)-3-hydroxyp...) Show SMILES CN([C@H](CN1CC[C@H](O)C1)c1ccccc1)C(=O)CC(=O)NCc1ccccc1 Show InChI InChI=1S/C23H29N3O3/c1-25(23(29)14-22(28)24-15-18-8-4-2-5-9-18)21(19-10-6-3-7-11-19)17-26-13-12-20(27)16-26/h2-11,20-21,27H,12-17H2,1H3,(H,24,28)/t20-,21+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	3.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Adolor Corporation Curated by ChEMBL					Assay Description Inhibition of CYP2D6				Bioorg Med Chem Lett 17: 1951-5 (2007) Article DOI: 10.1016/j.bmcl.2007.01.053 BindingDB Entry DOI: 10.7270/Q2Q52P9X
					More data for this Ligand-Target Pair