Compile Data Set for Download or QSAR
Report error Found 262 Enz. Inhib. hit(s) with Target = 'Chymotrypsin-C'
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM23716(N-{4-[(3-methyl-1H-pyrazol-1-yl)carbonyl]phenyl}ac...)
Affinity DataAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2008
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM23718(1-[(2-methylphenyl)carbonyl]-1H-pyrazole | N-Benzo...)
Affinity DataAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2008
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM23724(1-[(2-bromophenyl)carbonyl]-1H-pyrazole | N-Benzoy...)
Affinity DataAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2008
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM93332(QN-33)
Affinity DataKd:  2.53E+4nMpH: 7.4Assay Description:Fluorescence titration using alpha-chymotrypsin.More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/10/2013
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM93333(Met-33)
Affinity DataKd:  1.10E+5nMpH: 7.4Assay Description:Fluorescence titration using alpha-chymotrypsin.More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/10/2013
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM93334(Sul-33)
Affinity DataKd:  3.51E+5nMpH: 7.4Assay Description:Fluorescence titration using alpha-chymotrypsin.More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/10/2013
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM93335(QN-49)
Affinity DataKd:  2.24E+4nMpH: 7.4Assay Description:Fluorescence titration using alpha-chymotrypsin.More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/10/2013
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM93336(Met-49)
Affinity DataKd:  4.10E+4nMpH: 7.4Assay Description:Fluorescence titration using alpha-chymotrypsin.More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/10/2013
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM93337(Sul-49)
Affinity DataKd:  1.90E+5nMpH: 7.4Assay Description:Fluorescence titration using alpha-chymotrypsin.More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/10/2013
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM93338(Neu-49)
Affinity DataKd: >5.00E+5nMpH: 7.4Assay Description:Fluorescence titration using alpha-chymotrypsin.More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/10/2013
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50101132(1,3-Dibenzyl-[1,3]diazetidine-2,4-dione | CHEMBL47...)
Affinity DataIC50: 0.690nMAssay Description:Compound was evaluated for its inhibitory activity against bovine pancreatic alpha-chymotrypsinMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50101131(1,3-Di-p-tolyl-[1,3]diazetidine-2,4-dione | CHEMBL...)
Affinity DataIC50: 2.40nMAssay Description:Compound was evaluated for its inhibitory activity against bovine pancreatic alpha-chymotrypsinMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50072290((3S,3aR,6aS)-3-Allyl-hexahydro-cyclopenta[b]furan-...)
Affinity DataIC50: 7nMAssay Description:Compound was evaluated for the inhibition of ChymotrypsinogenMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM23700(methyl 1-[(4-chlorophenyl)carbonyl]-1H-pyrazole-5-...)
Affinity DataIC50: 15nMAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2008
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM23705(4-bromo-1-[(4-methylphenyl)carbonyl]-1H-pyrazole |...)
Affinity DataIC50: 15nMAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2008
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50072282((3R,3aR,6aS)-3-Allyl-hexahydro-cyclopenta[b]furan-...)
Affinity DataIC50: 37nMAssay Description:Compound was evaluated for the inhibition of ChymotrypsinogenMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM23698(4-chloro-1-[(4-fluorophenyl)carbonyl]-1H-pyrazole ...)
Affinity DataIC50: 40nMAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2008
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM23709(3-methyl-1-[(3,4,5-trimethoxyphenyl)carbonyl]-1H-p...)
Affinity DataIC50: 50nMAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2008
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50120284(Peptide Boronic Acid analogue | CHEMBL107656)
Affinity DataIC50: 50nMAssay Description:Inhibitory concentration against Human pancreatic Serine protease chymotrypsinMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM23704(1-benzoyl-N-phenyl-1H-pyrazole-3-carboxamide | N-B...)
Affinity DataIC50: 57nMAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2008
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50120311(Peptide Boronic Acid analogue | CHEMBL320814)
Affinity DataIC50: 65nMAssay Description:Inhibitory concentration against Human pancreatic Serine protease chymotrypsinMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50072284((1S,2R,4aR,6aS,6bS,7R,9aS,10aS)-2-Acetoxy-1,4a,6a,...)
Affinity DataIC50: 70nMAssay Description:Compound was evaluated for the inhibition of ChymotrypsinogenMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50120309(Peptide Boronic Acid analogue | CHEMBL108189)
Affinity DataIC50: 70nMAssay Description:Inhibitory concentration against Human pancreatic Serine protease chymotrypsinMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50120298(Peptide Boronic Acid analogue | CHEMBL109434)
Affinity DataIC50: 75nMAssay Description:Inhibitory concentration against Human pancreatic Serine protease chymotrypsinMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50072283((3S,3aR,6aS)-3-Benzyl-hexahydro-cyclopenta[b]furan...)
Affinity DataIC50: 100nMAssay Description:Compound was evaluated for the inhibition of ChymotrypsinogenMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50072286((3R,3aR,6aS)-3-Benzyl-hexahydro-cyclopenta[b]furan...)
Affinity DataIC50: 100nMAssay Description:Compound was evaluated for the inhibition of ChymotrypsinogenMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50072289((3S,3aR,6aS)-3-(4-Methyl-2-oxo-pent-3-enyl)-hexahy...)
Affinity DataIC50: 100nMAssay Description:Compound was evaluated for the inhibition of ChymotrypsinogenMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50072292((3S,3aS,6aS)-3-Phenylsulfanyl-hexahydro-cyclopenta...)
Affinity DataIC50: 100nMAssay Description:Compound was evaluated for the inhibition of ChymotrypsinogenMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50072285((3R,3aS,6aS)-3-Phenylsulfanyl-hexahydro-cyclopenta...)
Affinity DataIC50: 100nMAssay Description:Compound was evaluated for the inhibition of ChymotrypsinogenMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM23702(3-[(2,4-dimethylphenyl)carbonyl]-1-[(4-fluoropheny...)
Affinity DataIC50: 120nMAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2008
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM23706(1-[(3,4-dichlorophenyl)carbonyl]-1H-pyrazole | N-B...)
Affinity DataIC50: 125nMAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2008
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50093722((6R,7R)-3-(4-Carboxymethyl-4H-[1,2,4]triazol-3-yls...)
Affinity DataIC50: 160nMAssay Description:The compound was evaluated for the inhibitory activity against alpha-chymotrypsinMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM23710(1-[(4-methylphenyl)carbonyl]-3-nitro-1H-pyrazole |...)
Affinity DataIC50: 190nMAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2008
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM23712(1-[(2-methylphenyl)carbonyl]-4-nitro-1H-pyrazole |...)
Affinity DataIC50: 240nMAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2008
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50120286(Peptide Boronic Acid analogue | CHEMBL322933)
Affinity DataIC50: 280nMAssay Description:Inhibitory concentration against Human pancreatic Serine protease chymotrypsinMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50096724((S)-4-((S)-1-{(S)-1-[(S)-1-((R)-1-Aminooxalyl-pent...)
Affinity DataIC50: 300nMAssay Description:Compound was tested for inhibition of Serine protease chymotrypsinMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50120292(Peptide Boronic Acid analogue | CHEMBL322110)
Affinity DataIC50: 300nMAssay Description:Inhibitory concentration against Human pancreatic Serine protease chymotrypsinMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM23701(4-chloro-1-[(3-nitrophenyl)carbonyl]-1H-pyrazole |...)
Affinity DataIC50: 340nMAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2008
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50120288(Peptide Boronic Acid analogue | CHEMBL432978)
Affinity DataIC50: 380nMAssay Description:Inhibitory concentration against Human pancreatic Serine protease chymotrypsinMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50120305(Peptide Boronic Acid analogue | CHEMBL111765)
Affinity DataIC50: 420nMAssay Description:Inhibitory concentration against Human pancreatic Serine protease chymotrypsinMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50101133(1,3-Diethyl-[1,3]diazetidine-2,4-dione | CHEMBL298...)
Affinity DataIC50: 740nMAssay Description:Compound was evaluated for its inhibitory activity against bovine pancreatic alpha-chymotrypsinMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50291321({1-[1-(1-Benzyl-2-oxo-ethylcarbamoyl)-ethylcarbamo...)
Affinity DataIC50: 950nMAssay Description:The compound was tested for the inhibition of alpha-Chymotrypsin, activity expressed as IC50More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/22/2010
Entry Details Article

TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50135493(5-Fluoro-3-methyl-benzo[b]thiophene-2-sulfonic aci...)
Affinity DataIC50: 1.00E+3nMAssay Description:In vitro inhibitory activity against bovin chymotrypsinMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50135495(4-(5-Chloro-3-methyl-benzo[b]thiophene-2-sulfonyla...)
Affinity DataIC50: 1.00E+3nMAssay Description:In vitro inhibitory activity against bovin chymotrypsinMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50135494(4-(5-Fluoro-3-methyl-benzo[b]thiophene-2-sulfonyla...)
Affinity DataIC50: 1.00E+3nMAssay Description:In vitro inhibitory activity against bovin chymotrypsinMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM50167307(1-Benzo[b]thiophen-2-ylmethyl-5-iodo-1H-indole-2,3...)
Affinity DataIC50: 1.00E+3nMAssay Description:In vitro inhibitory concentration against Chymotrypsin (serine protease)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM23707(1-[(2-fluorophenyl)carbonyl]-5-methyl-3-nitro-1H-p...)
Affinity DataIC50: 1.20E+3nMAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2008
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM23717(4-chloro-1-[(2-chlorophenyl)carbonyl]-1H-pyrazole ...)
Affinity DataIC50: 1.40E+3nMAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2008
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM23720(1-[(4-tert-butylphenyl)carbonyl]-4-chloro-1H-pyraz...)
Affinity DataIC50: 1.50E+3nMAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2008
Entry Details Article
PubMed
TargetChymotrypsin-C(Human)
Montana State University

LigandPNGBDBM23708(4-bromo-1-[(2,6-difluorophenyl)carbonyl]-1H-pyrazo...)
Affinity DataIC50: 1.80E+3nMAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2008
Entry Details Article
PubMed
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