null

SMILES: CN([C@H](CN1CC[C@H](O)C1)c1ccccc1)C(=O)CCC(=O)Nc1cccnc1

InChI Key: InChIKey=OAZNVARZWJKVRZ-VQTJNVASSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50205680   

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))	BDBM50205680 (CHEMBL230711 | N1-((S)-2-((S)-3-hydroxypyrrolidin-...) Show SMILES CN([C@H](CN1CC[C@H](O)C1)c1ccccc1)C(=O)CCC(=O)Nc1cccnc1 Show InChI InChI=1S/C22H28N4O3/c1-25(22(29)10-9-21(28)24-18-8-5-12-23-14-18)20(17-6-3-2-4-7-17)16-26-13-11-19(27)15-26/h2-8,12,14,19-20,27H,9-11,13,15-16H2,1H3,(H,24,28)/t19-,20+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	280	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))	BDBM50205680 (CHEMBL230711 | N1-((S)-2-((S)-3-hydroxypyrrolidin-...) Show SMILES CN([C@H](CN1CC[C@H](O)C1)c1ccccc1)C(=O)CCC(=O)Nc1cccnc1 Show InChI InChI=1S/C22H28N4O3/c1-25(22(29)10-9-21(28)24-18-8-5-12-23-14-18)20(17-6-3-2-4-7-17)16-26-13-11-19(27)15-26/h2-8,12,14,19-20,27H,9-11,13,15-16H2,1H3,(H,24,28)/t19-,20+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>1.00E+4	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