null

SMILES: CN([C@H](CN1CC[C@H](O)C1)c1ccccc1)C(=O)NCC(=O)Nc1ccccc1

InChI Key: InChIKey=WSFQCNYXQWFYJC-VQTJNVASSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50205683   

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))	BDBM50205683 (1-((S)-2-((S)-3-hydroxypyrrolidin-1-yl)-1-phenylet...) Show SMILES CN([C@H](CN1CC[C@H](O)C1)c1ccccc1)C(=O)NCC(=O)Nc1ccccc1 Show InChI InChI=1S/C22H28N4O3/c1-25(22(29)23-14-21(28)24-18-10-6-3-7-11-18)20(17-8-4-2-5-9-17)16-26-13-12-19(27)15-26/h2-11,19-20,27H,12-16H2,1H3,(H,23,29)(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	Article PubMed	6.5	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))	BDBM50205683 (1-((S)-2-((S)-3-hydroxypyrrolidin-1-yl)-1-phenylet...) Show SMILES CN([C@H](CN1CC[C@H](O)C1)c1ccccc1)C(=O)NCC(=O)Nc1ccccc1 Show InChI InChI=1S/C22H28N4O3/c1-25(22(29)23-14-21(28)24-18-10-6-3-7-11-18)20(17-8-4-2-5-9-17)16-26-13-12-19(27)15-26/h2-11,19-20,27H,12-16H2,1H3,(H,23,29)(H,24,28)/t19-,20+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.10E+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