BDBM50319968 CHEMBL1085780::N-benzyl-2-(pyrrolidin-1-yl)pyrimidin-4-amine

SMILES C(Nc1ccnc(n1)N1CCCC1)c1ccccc1

InChI Key InChIKey=PGBNXXDXGXQQRQ-UHFFFAOYSA-N

Data  4 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 = 50319968   

TargetAcetylcholinesterase(Human)
University of Waterloo

Curated by ChEMBL
LigandPNGBDBM50319968(N-benzyl-2-(pyrrolidin-1-yl)pyrimidin-4-amine | CH...)
Affinity DataIC50: 8.70E+3nMAssay Description:Inhibition of human AChE incubated with compounf for 5 mins before addition of substrate acetylthiocholine iodide by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
University of Waterloo

Curated by ChEMBL
LigandPNGBDBM50319968(N-benzyl-2-(pyrrolidin-1-yl)pyrimidin-4-amine | CH...)
Affinity DataIC50: 9.80E+3nMAssay Description:Inhibition of electric eel AChEMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
TargetCarboxylic ester hydrolase(Horse)
University of Waterloo

Curated by ChEMBL
LigandPNGBDBM50319968(N-benzyl-2-(pyrrolidin-1-yl)pyrimidin-4-amine | CH...)
Affinity DataIC50: 2.64E+4nMAssay Description:Inhibition of equine BChE incubated with compounf for 5 mins before addition of substrate S-butyrylthiocholine iodide by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMed
TargetCholinesterase(Horse)
University of Waterloo

Curated by ChEMBL
LigandPNGBDBM50319968(N-benzyl-2-(pyrrolidin-1-yl)pyrimidin-4-amine | CH...)
Affinity DataIC50: 2.64E+4nMAssay Description:Inhibition of equine serum BuChEMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed