BDBM50272035 (2S,5R)-5-cyclohexyl-2-[(4-methoxyphenyl)methyl]-1-[(4-methylcyclohexyl)methyl]-1H,2H,3H,5H,6H-imidazo[1,2-a]imidazolidin-7-ium

SMILES COc1ccc(CC2C[N+]3=C(NCC3C3CCCCC3)N2CC2CCC(C)CC2)cc1

InChI Key InChIKey=OPNCBMYHRCYEGA-UHFFFAOYSA-O

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50272035   

TargetKappa-type opioid receptor(Homo sapiens (Human))
Torrey Pines Institute For Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50272035((2S,5R)-5-cyclohexyl-2-[(4-methoxyphenyl)methyl]-1...)
Affinity DataIC50:  804nMAssay Description:Inhibitory activity for kappa opioid receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Cavia porcellus (domestic guinea pig))
Torrey Pines Institute For Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50272035((2S,5R)-5-cyclohexyl-2-[(4-methoxyphenyl)methyl]-1...)
Affinity DataIC50:  804nMAssay Description:Displacement of [3H]U69593 from kappa opioid receptor in guinea pig brain homogenateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
Torrey Pines Institute For Molecular Studies

Curated by ChEMBL
LigandPNGBDBM50272035((2S,5R)-5-cyclohexyl-2-[(4-methoxyphenyl)methyl]-1...)
Affinity DataIC50:  2.97E+3nMAssay Description:Inhibition of Opioid receptor kappa 1 bindingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed