Compile Data Set for Download or QSAR
Report error Found 150 Enz. Inhib. hit(s) with all data for entry = 50009579
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085348(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-p-tolyl-p...)
Affinity DataIC50: 300nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085351(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(2-fluoro...)
Affinity DataIC50: 360nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085352(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(2,3-dich...)
Affinity DataIC50: 400nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085339(((S)-1-Benzyl-3-chloro-2-oxo-propyl)-carbamic acid...)
Affinity DataIC50: 400nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085338(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-m-tolyl-p...)
Affinity DataIC50: 430nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085343(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(2-chloro...)
Affinity DataIC50: 600nMAssay Description:Inhibitory activity against human serine protease chymaseMore 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
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085347(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(3-methox...)
Affinity DataIC50: 730nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085358(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-o-tolyl-p...)
Affinity DataIC50: 780nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085342(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(2,3-dime...)
Affinity DataIC50: 890nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085364(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(3-chloro...)
Affinity DataIC50: 890nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085344(5-Phenyl-pentanoic acid ((S)-1-benzyl-3-chloro-2-o...)
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085365(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(3-fluoro...)
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085360(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-benzamide |...)
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085353(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(4-ethyl-...)
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085361(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(3-hydrox...)
Affinity DataIC50: 1.80E+3nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085341(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(3-triflu...)
Affinity DataIC50: 1.90E+3nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085355(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(4-chloro...)
Affinity DataIC50: 1.90E+3nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085356(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(2-methox...)
Affinity DataIC50: 2.10E+3nMAssay 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
LigandPNGBDBM50085342(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(2,3-dime...)
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibitory activity against alpha-chymotrypsin (alpha-CT)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085350(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(3,4-dime...)
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085366(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(4-methox...)
Affinity DataIC50: 2.20E+3nMAssay 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
LigandPNGBDBM50085366(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(4-methox...)
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibitory activity against alpha-chymotrypsin (alpha-CT)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085359(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(4-fluoro...)
Affinity DataIC50: 2.40E+3nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085357(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-4-phenyl-bu...)
Affinity DataIC50: 2.50E+3nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085354(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(4-triflu...)
Affinity DataIC50: 2.50E+3nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085345(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(4-hydrox...)
Affinity DataIC50: 2.70E+3nMAssay 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
LigandPNGBDBM50085356(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(2-methox...)
Affinity DataIC50: 2.70E+3nMAssay Description:Inhibitory activity against alpha-chymotrypsin (alpha-CT)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085340(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(4-isopro...)
Affinity DataIC50: 3.10E+3nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085363(N-Tosyl-L-phenylalanine chloromethyl ketone | CHEM...)
Affinity DataIC50: 3.30E+3nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085346(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(3,4-dich...)
Affinity DataIC50: 3.70E+3nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetTrypsin(Pig)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085340(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(4-isopro...)
Affinity DataIC50: 4.00E+3nMAssay Description:Inhibitory activity against porcine pancreatic trypsin (TRP)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymotrypsinogen A(Bovine)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085346(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(3,4-dich...)
Affinity DataIC50: 4.20E+3nMAssay Description:Inhibitory activity against alpha-chymotrypsin (alpha-CT)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085367(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-2-phenyl-ac...)
Affinity DataIC50: 4.70E+3nMAssay 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
LigandPNGBDBM50085361(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(3-hydrox...)
Affinity DataIC50: 5.20E+3nMAssay Description:Inhibitory activity against alpha-chymotrypsin (alpha-CT)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin G(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085346(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(3,4-dich...)
Affinity DataIC50: 8.10E+3nMAssay Description:Inhibitory activity against human leukocyte cathepsin GMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymotrypsinogen A(Bovine)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085362(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-phenyl-ac...)
Affinity DataIC50: 8.70E+3nMAssay Description:Inhibitory activity against alpha-chymotrypsin (alpha-CT)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymotrypsinogen A(Bovine)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085360(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-benzamide |...)
Affinity DataIC50: 9.30E+3nMAssay Description:Inhibitory activity against alpha-chymotrypsin (alpha-CT)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin G(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085366(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(4-methox...)
Affinity DataIC50: 9.30E+3nMAssay Description:Inhibitory activity against human leukocyte cathepsin GMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymotrypsinogen A(Bovine)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085352(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(2,3-dich...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against alpha-chymotrypsin (alpha-CT)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin G(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085356(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(2-methox...)
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibitory activity against human leukocyte cathepsin GMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymotrypsinogen A(Bovine)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085338(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-m-tolyl-p...)
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibitory activity against alpha-chymotrypsin (alpha-CT)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymotrypsinogen A(Bovine)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085358(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-o-tolyl-p...)
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibitory activity against alpha-chymotrypsin (alpha-CT)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin G(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085344(5-Phenyl-pentanoic acid ((S)-1-benzyl-3-chloro-2-o...)
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibitory activity against human leukocyte cathepsin GMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin G(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085367(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-2-phenyl-ac...)
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibitory activity against human leukocyte cathepsin GMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymotrypsin-like elastase family member 2A(Pig)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085354(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(4-triflu...)
Affinity DataIC50: 1.30E+4nMAssay Description:Inhibitory activity against porcine pancreatic elastase (PPE)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymotrypsinogen A(Bovine)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085345(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(4-hydrox...)
Affinity DataIC50: 1.40E+4nMAssay Description:Inhibitory activity against alpha-chymotrypsin (alpha-CT)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymase(Human)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085362(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-phenyl-ac...)
Affinity DataIC50: 1.50E+4nMAssay Description:Inhibitory activity against human serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymotrypsin-like elastase family member 2A(Pig)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085340(N-((S)-1-Benzyl-3-chloro-2-oxo-propyl)-3-(4-isopro...)
Affinity DataIC50: 1.50E+4nMAssay Description:Inhibitory activity against porcine pancreatic elastase (PPE)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetChymotrypsinogen A(Bovine)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50085339(((S)-1-Benzyl-3-chloro-2-oxo-propyl)-carbamic acid...)
Affinity DataIC50: 1.70E+4nMAssay Description:Inhibitory activity against alpha-chymotrypsin (alpha-CT)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
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