BDBM50382109 CHEMBL2023319

SMILES Clc1ccc(-c2cc(C=O)no2)c(Cl)c1

InChI Key InChIKey=BVUVSNNTQGPIAE-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 = 50382109   

TargetAcrosin(Human)
Second Military Medical University

Curated by ChEMBL
LigandPNGBDBM50382109(CHEMBL2023319)
Affinity DataIC50:  3.90E+5nMAssay Description:Inhibition of human acrosin using N-alpha-benzoyl-L-arginine p-nitroanilide as substrate after 3 hrs by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetAcrosin(Human)
Second Military Medical University

Curated by ChEMBL
LigandPNGBDBM50382109(CHEMBL2023319)
Affinity DataIC50:  1.70E+6nMAssay Description:Inhibition of acrosin in human spermatozoa assessed as effect on amidase activity after 3 hrs incubation by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetAcrosin(Human)
Second Military Medical University

Curated by ChEMBL
LigandPNGBDBM50382109(CHEMBL2023319)
Affinity DataIC50:  3.90E+5nMAssay Description:Inhibition of human sperm acrosin using BAPNA as substrate after 3 hrs by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetAcrosin(Human)
Second Military Medical University

Curated by ChEMBL
LigandPNGBDBM50382109(CHEMBL2023319)
Affinity DataIC50:  3.90E+7nMAssay Description:Inhibition of human acrosin using N-alpha-benzoyl-DL-arginine para-nitroanilide-HCl as substrate after 3 hrs by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed