BDBM50323669 (1R,6S,5R)-[6-(2-(Pyridin-3-yl)phenoxy))]-3-azabicyclo[3.2.1]octane hydrochloride::CHEMBL1209070::rac-exo-[6-(2-(pyridin-3-yl)phenoxy))]-3-azabicyclo[3.2.1]octane hydrochloride

SMILES C1[C@@H]2C[C@H](Oc3ccccc3-c3cccnc3)[C@H]1CNC2

InChI Key InChIKey=HXZFPBBYBMMKAQ-SIIHOXLZSA-N

Data  4 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50323669   

TargetNeuronal acetylcholine receptor subunit alpha-4/beta-2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50323669((1R,6S,5R)-[6-(2-(Pyridin-3-yl)phenoxy))]-3-azabic...)
Affinity DataKi: >1.30E+3nMAssay Description:Displacement of [3H]epibatidine from alpha4beta2 nicotinic receptor expressed in human HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeuronal acetylcholine receptor subunit alpha-4/beta-2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50323669((1R,6S,5R)-[6-(2-(Pyridin-3-yl)phenoxy))]-3-azabic...)
Affinity DataKi: >1.31E+3nMAssay Description:Displacement of [3H]epibatidine from alpha4beta2 nicotinic receptor expressed in human HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50323669((1R,6S,5R)-[6-(2-(Pyridin-3-yl)phenoxy))]-3-azabic...)
Affinity DataKi:  2.16E+3nMAssay Description:Displacement of [3H]dofetilide from human ERG expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeuronal acetylcholine receptor subunit alpha-7(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50323669((1R,6S,5R)-[6-(2-(Pyridin-3-yl)phenoxy))]-3-azabic...)
Affinity DataKi:  3.30E+3nMAssay Description:Displacement of [3H]epibatidine from alpha7 nicotinic receptor expressed in human HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed