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SMILES: O=c1c(ccnn1C(CN1CCCC1)c1ccccc1)-c1ccccc1

InChI Key: InChIKey=ZQDCQWNIDZCDEA-UHFFFAOYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50125462   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50125462
PNG
(4-Phenyl-2-(1-phenyl-2-pyrrolidin-1-yl-ethyl)-2H-p...)
Show SMILES O=c1c(ccnn1C(CN1CCCC1)c1ccccc1)-c1ccccc1
Show InChI InChI=1S/C22H23N3O/c26-22-20(18-9-3-1-4-10-18)13-14-23-25(22)21(17-24-15-7-8-16-24)19-11-5-2-6-12-19/h1-6,9-14,21H,7-8,15-17H2
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PC cid
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n/an/a 550n/an/an/an/an/an/a



AstraZeneca R&D

Curated by ChEMBL


Assay Description
Inhibition of [125I]-(D-Pro10)-Dynorphin A binding to human kappa opioid receptor from membranes of HEK293 cells


Bioorg Med Chem Lett 13: 1141-5 (2003)


BindingDB Entry DOI: 10.7270/Q24J0DH2
More data for this
Ligand-Target Pair