BDBM50319973 CHEMBL1082978::N-phenethyl-2-(pyrrolidin-1-yl)pyrimidin-4-amine

SMILES C(Cc1ccccc1)Nc1ccnc(n1)N1CCCC1

InChI Key InChIKey=MIALFBONYMMUFB-UHFFFAOYSA-N

Data  4 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50319973   

TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
University Of Waterloo

Curated by ChEMBL
LigandPNGBDBM50319973(CHEMBL1082978 | N-phenethyl-2-(pyrrolidin-1-yl)pyr...)
Affinity DataIC50:  1.20E+4nMAssay Description:Inhibition of electric eel AChEMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
University Of Waterloo

Curated by ChEMBL
LigandPNGBDBM50319973(CHEMBL1082978 | N-phenethyl-2-(pyrrolidin-1-yl)pyr...)
Affinity DataIC50:  9.80E+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 DepthDetails ArticlePubMed
TargetCarboxylic ester hydrolase(Equus caballus (Horse))
University Of Waterloo

Curated by ChEMBL
LigandPNGBDBM50319973(CHEMBL1082978 | N-phenethyl-2-(pyrrolidin-1-yl)pyr...)
Affinity DataIC50:  1.38E+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 DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
University Of Waterloo

Curated by ChEMBL
LigandPNGBDBM50319973(CHEMBL1082978 | N-phenethyl-2-(pyrrolidin-1-yl)pyr...)
Affinity DataIC50:  1.38E+4nMAssay Description:Inhibition of equine serum BuChEMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed