BDBM50327278 CHEMBL1257459::endo-3-(8-((R)-1-(2-chloropyridin-4-yl)ethyl)-8-azabicyclo[3.2.1]octan-3-yloxy)benzamide

SMILES C[C@@H](N1[C@H]2CC[C@@H]1C[C@H](C2)Oc1cccc(c1)C(N)=O)c1ccnc(Cl)c1

InChI Key InChIKey=COVZSEBDZICBKI-UEILYKACSA-N

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 = 50327278   

TargetKappa-type opioid receptor(Homo sapiens (Human))
Astrazeneca Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50327278(CHEMBL1257459 | endo-3-(8-((R)-1-(2-chloropyridin-...)
Affinity DataIC50:  307nMAssay Description:Antagonist activity at human kappa opioid receptor assessed as inhibition of dynorphin A-induced [35S]GTPgammaS bindingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Astrazeneca Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50327278(CHEMBL1257459 | endo-3-(8-((R)-1-(2-chloropyridin-...)
Affinity DataIC50:  13nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
Astrazeneca Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50327278(CHEMBL1257459 | endo-3-(8-((R)-1-(2-chloropyridin-...)
Affinity DataIC50:  2.29E+4nMAssay Description:Antagonist activity at human mu opioid receptor assessed as inhibition of DAMGO-stimulated [35S]GTPgammaS bindingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed