BDBM50085349 CHEMBL64495::N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-phenyl-propionamide

SMILES ClCC(=O)[C@H](Cc1ccccc1)NC(=O)CCc1ccccc1

InChI Key InChIKey=CSVPVXZWSSCWON-UHFFFAOYSA-N

Data  5 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50085349   

TargetChymotrypsin-like elastase family member 2A(Pig)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085349(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-phenyl-pr...)
Affinity DataIC50: 1.50E+5nMAssay Description:Inhibitory activity against porcine pancreatic elastase (PPE)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin G(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085349(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-phenyl-pr...)
Affinity DataIC50: 6.30E+4nMAssay Description:Inhibitory activity against human leukocyte cathepsin GMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085349(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-phenyl-pr...)
Affinity DataIC50: 710nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymotrypsinogen A(Bovine)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085349(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-phenyl-pr...)
Affinity DataIC50: 3.70E+4nMAssay Description:Inhibitory activity against alpha-chymotrypsin (alpha-CT)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetTrypsin(Pig)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085349(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-phenyl-pr...)
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibitory activity against porcine pancreatic trypsin (TRP)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed