BDBM50382467 CHEMBL2024089

SMILES CNC(=O)OCC[C@H]1C[C@@H]1c1cncc(OC[C@@H]2CCN2)c1

InChI Key InChIKey=HGSHFGWWOPXUPH-WHOFXGATSA-N

Data  2 KI  1 IC50  1 EC50

  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 4 hits for monomerid = 50382467   

TargetAcetylcholine-binding protein(Lymnaea stagnalis)
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50382467(CHEMBL2024089)
Affinity DataKi:  22nMAssay Description:Displacement of [3H]epibatidine from Lymnaea stagnalis AChBPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSoluble acetylcholine receptor(Aplysia Californica)
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50382467(CHEMBL2024089)
Affinity DataKi:  1.93E+3nMAssay Description:Displacement of [3H]epibatidine from Aplysia californica AChBPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeuronal acetylcholine receptor subunit alpha-4/beta-2(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50382467(CHEMBL2024089)
Affinity DataIC50:  18.2nMAssay Description:Antagonist activity at human alpha4beta2 nAChR expressed in SH-EP1 cells assessed as inhibition of carbamylcholine induced 86Rb+ ion efflux preincuba...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeuronal acetylcholine receptor subunit alpha-4/beta-2(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50382467(CHEMBL2024089)
Affinity DataEC50:  15.7nMAssay Description:Agonist activity at human alpha4beta2 nAChR expressed in SH-EP1 cells assessed as 86Rb+ ion efflux after 9.5 mins by flip-plate techniqueMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed