BDBM50359285 CHEMBL1928380

SMILES CCC(=O)Oc1ccc(COC(=O)Nc2ccncc2N)cc1

InChI Key InChIKey=YVGCOQPYXUZHJT-UHFFFAOYSA-N

Data  2 KI  2 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 = 50359285   

TargetAcetylcholinesterase(Electric eel)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50359285(CHEMBL1928380)
Affinity DataKi:  5.70E+3nMAssay Description:Inhibition of Electrophorus electricus Type V-S acetylcholinesterase using acetylcholine iodide as substrate by spectrophotometric Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarboxylic ester hydrolase(Horse)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50359285(CHEMBL1928380)
Affinity DataKi:  2.50E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as a substrate by spectrophotometric Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electric eel)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50359285(CHEMBL1928380)
Affinity DataIC50:  5.20E+3nMAssay Description:Inhibition of Electrophorus electricus Type V-S acetylcholinesterase using acetylcholine iodide as substrate by spectrophotometric Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarboxylic ester hydrolase(Horse)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50359285(CHEMBL1928380)
Affinity DataIC50:  1.29E+5nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as a substrate by spectrophotometric Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed