BDBM50143302 (S)-1-dodecyl-3-(1-methylpyrrolidin-2-yl)pyridinium iodide::1-Dodecyl-3-((S)-1-methyl-pyrrolidin-2-yl)-pyridinium; iodide::CHEMBL55606

SMILES CCCCCCCCCCCC[n+]1cccc(c1)[C@@H]1CCCN1C

InChI Key InChIKey=NAVBJWWCUOXXQB-QFIPXVFZSA-N

Data  3 KI  1 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 4 hits for monomerid = 50143302   

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

Curated by ChEMBL
LigandPNGBDBM50143302((S)-1-dodecyl-3-(1-methylpyrrolidin-2-yl)pyridiniu...)
Affinity DataKi:  0.140nMAssay Description:Binding affinity to alpha4beta2 nAChR (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeuronal acetylcholine receptor subunit alpha-4/beta-2(Rattus norvegicus (Rat))
University Of Kentucky

Curated by ChEMBL
LigandPNGBDBM50143302((S)-1-dodecyl-3-(1-methylpyrrolidin-2-yl)pyridiniu...)
Affinity DataKi:  140nMAssay Description:Inhibitory activity of the compound against nAChR mediated nicotine-evoked [3H]-DA overflow using rat striatal slicesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeuronal acetylcholine receptor subunit alpha-7(Rattus norvegicus (Rat))
Universit£

Curated by ChEMBL
LigandPNGBDBM50143302((S)-1-dodecyl-3-(1-methylpyrrolidin-2-yl)pyridiniu...)
Affinity DataKi:  8.30E+4nMAssay Description:Displacement of [125I]alpha-bungarotoxin from alpha7 nAChR in Sprague-Dawley rat hippocampus membrane homogenates by gamma countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeuronal acetylcholine receptor subunit alpha-4/beta-2(Rattus norvegicus (Rat))
University Of Kentucky

Curated by ChEMBL
LigandPNGBDBM50143302((S)-1-dodecyl-3-(1-methylpyrrolidin-2-yl)pyridiniu...)
Affinity DataIC50:  9nMAssay Description:Inhibitory activity of the compound against nAChR mediated nicotine-evoked [3H]-DA overflow using rat striatal slicesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed