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Found 1273 Enz. Inhib. hit(s) with Target = 'Chymotrypsin'
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM50018175(CHEMBL22389 | N-{1-Benzyl-2-[(pyridine-3-carbonyl)...)
Affinity DataKi:  4.80E+4nMpH: 5.0Assay Description:Inhibition of chymotrypsin-catalyzed hydrolysis of BzArg p-nitroanilide by compound at pH 5More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM50018174(CHEMBL283109 | N-{2-[(2-Acetylamino-propionyl)-hyd...)
Affinity DataKi:  4.80E+4nMpH: 5.0Assay Description:Inhibition of papain-catalyzed hydrolysis of BzArg p-nitroanilide by compound at pH 5.5More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM50018175(CHEMBL22389 | N-{1-Benzyl-2-[(pyridine-3-carbonyl)...)
Affinity DataKi:  4.80E+4nMpH: 5.0Assay Description:Inhibition of chymotrypsin-catalyzed hydrolysis of BzArg p-nitroanilide by compound at pH 7.8More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM50018173(CHEMBL22745 | N-{2-[(2-Acetylamino-propionyl)-hydr...)
Affinity DataKi: >8.00E+6nMpH: 5.0Assay Description:Inhibition of chymotrypsin-catalyzed hydrolysis of BzArg p-nitroanilide by compound at pH 5More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM50018174(CHEMBL283109 | N-{2-[(2-Acetylamino-propionyl)-hyd...)
Affinity DataKi:  3.10E+4nMpH: 7.0Assay Description:Initial rate of reaction between Chymotrypsinogen and BzArg p-nitro-anilide in the presence of 400 microM of the compound at pH 7More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM113248(US9695194, 7)
Affinity DataKi: <100nM ΔG°: <-41.6kJ/molepH: 7.2 T: 2°CAssay Description:Materials: Chymotrypsin, bovine, 25 ug (Roche, sequence grade), Substrate S-2586 (Chromogenics, cat. no. 82 08 94). Chymotrypsin activity was determi...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM113283(US9695194, 8)
Affinity DataKi: <100nM ΔG°: <-41.6kJ/molepH: 7.2 T: 2°CAssay Description:Materials: Chymotrypsin, bovine, 25 ug (Roche, sequence grade), Substrate S-2586 (Chromogenics, cat. no. 82 08 94). Chymotrypsin activity was determi...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM113296(US9695194, 13)
Affinity DataKi: <100nM ΔG°: <-41.6kJ/molepH: 7.2 T: 2°CAssay Description:Materials: Chymotrypsin, bovine, 25 ug (Roche, sequence grade), Substrate S-2586 (Chromogenics, cat. no. 82 08 94). Chymotrypsin activity was determi...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM113119(US9695194, 6)
Affinity DataKi: <100nM ΔG°: <-41.6kJ/molepH: 7.2 T: 2°CAssay Description:Materials: Chymotrypsin, bovine, 25 ug (Roche, sequence grade), Substrate S-2586 (Chromogenics, cat. no. 82 08 94). Chymotrypsin activity was determi...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM113297(US9695194, 14)
Affinity DataKi: <100nM ΔG°: <-41.6kJ/molepH: 7.2 T: 2°CAssay Description:Materials: Chymotrypsin, bovine, 25 ug (Roche, sequence grade), Substrate S-2586 (Chromogenics, cat. no. 82 08 94). Chymotrypsin activity was determi...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM113300(US9695194, 16)
Affinity DataKi: <100nM ΔG°: <-41.6kJ/molepH: 7.2 T: 2°CAssay Description:Materials: Chymotrypsin, bovine, 25 ug (Roche, sequence grade), Substrate S-2586 (Chromogenics, cat. no. 82 08 94). Chymotrypsin activity was determi...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM113299(US9695194, 15)
Affinity DataKi: <100nM ΔG°: <-41.6kJ/molepH: 7.2 T: 2°CAssay Description:Materials: Chymotrypsin, bovine, 25 ug (Roche, sequence grade), Substrate S-2586 (Chromogenics, cat. no. 82 08 94). Chymotrypsin activity was determi...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM113293(US9695194, 10)
Affinity DataKi:  200nM ΔG°:  -39.8kJ/molepH: 7.2 T: 2°CAssay Description:Materials: Chymotrypsin, bovine, 25 ug (Roche, sequence grade), Substrate S-2586 (Chromogenics, cat. no. 82 08 94). Chymotrypsin activity was determi...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM113292(US9695194, 9)
Affinity DataKi:  400nM ΔG°:  -38.0kJ/molepH: 7.2 T: 2°CAssay Description:Materials: Chymotrypsin, bovine, 25 ug (Roche, sequence grade), Substrate S-2586 (Chromogenics, cat. no. 82 08 94). Chymotrypsin activity was determi...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM113295(US9695194, 12)
Affinity DataKi:  600nM ΔG°:  -36.9kJ/molepH: 7.2 T: 2°CAssay Description:Materials: Chymotrypsin, bovine, 25 ug (Roche, sequence grade), Substrate S-2586 (Chromogenics, cat. no. 82 08 94). Chymotrypsin activity was determi...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM113294(US9695194, 11)
Affinity DataKi:  1.00E+3nM ΔG°:  -35.6kJ/molepH: 7.2 T: 2°CAssay Description:Materials: Chymotrypsin, bovine, 25 ug (Roche, sequence grade), Substrate S-2586 (Chromogenics, cat. no. 82 08 94). Chymotrypsin activity was determi...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM113301(US9695194, 17)
Affinity DataKi:  1.20E+3nM ΔG°:  -35.2kJ/molepH: 7.2 T: 2°CAssay Description:Materials: Chymotrypsin, bovine, 25 ug (Roche, sequence grade), Substrate S-2586 (Chromogenics, cat. no. 82 08 94). Chymotrypsin activity was determi...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM50289001(2-(2-Iodo-phenyl)-6,7-dimethoxy-benzo[d][1,3]oxazi...)
Affinity DataKi: >1.00E+4nM ΔG°: >-29.7kJ/molepH: 7.2 T: 2°CAssay Description:Materials: Chymotrypsin, bovine, 25 ug (Roche, sequence grade), Substrate S-2586 (Chromogenics, cat. no. 82 08 94). Chymotrypsin activity was determi...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM113069(US9695194, 5)
Affinity DataKi: >1.00E+4nM ΔG°: >-29.7kJ/molepH: 7.2 T: 2°CAssay Description:Materials: Chymotrypsin, bovine, 25 ug (Roche, sequence grade), Substrate S-2586 (Chromogenics, cat. no. 82 08 94). Chymotrypsin activity was determi...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM113068(US9695194, 4)
Affinity DataKi: >1.00E+4nM ΔG°: >-29.7kJ/molepH: 7.2 T: 2°CAssay Description:Materials: Chymotrypsin, bovine, 25 ug (Roche, sequence grade), Substrate S-2586 (Chromogenics, cat. no. 82 08 94). Chymotrypsin activity was determi...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM113067(US9695194, 3)
Affinity DataKi: >1.00E+4nM ΔG°: >-29.7kJ/molepH: 7.2 T: 2°CAssay Description:Materials: Chymotrypsin, bovine, 25 ug (Roche, sequence grade), Substrate S-2586 (Chromogenics, cat. no. 82 08 94). Chymotrypsin activity was determi...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM113060(US9695194, 1)
Affinity DataKi: >1.00E+4nM ΔG°: >-29.7kJ/molepH: 7.2 T: 2°CAssay Description:Materials: Chymotrypsin, bovine, 25 ug (Roche, sequence grade), Substrate S-2586 (Chromogenics, cat. no. 82 08 94). Chymotrypsin activity was determi...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM113065(US9695194, 2)
Affinity DataKi: >1.00E+4nM ΔG°: >-29.7kJ/molepH: 7.2 T: 2°CAssay Description:Materials: Chymotrypsin, bovine, 25 ug (Roche, sequence grade), Substrate S-2586 (Chromogenics, cat. no. 82 08 94). Chymotrypsin activity was determi...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM93333(Met-33)
Affinity DataKd:  1.10E+5nMpH: 7.4Assay Description:Fluorescence titration using alpha-chymotrypsin.More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM93337(Sul-49)
Affinity DataKd:  1.90E+5nMpH: 7.4Assay Description:Fluorescence titration using alpha-chymotrypsin.More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails ArticlePubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM93336(Met-49)
Affinity DataKd:  4.10E+4nMpH: 7.4Assay Description:Fluorescence titration using alpha-chymotrypsin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM93335(QN-49)
Affinity DataKd:  2.24E+4nMpH: 7.4Assay Description:Fluorescence titration using alpha-chymotrypsin.More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM93332(QN-33)
Affinity DataKd:  2.53E+4nMpH: 7.4Assay Description:Fluorescence titration using alpha-chymotrypsin.More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM93338(Neu-49)
Affinity DataKd: >5.00E+5nMpH: 7.4Assay Description:Fluorescence titration using alpha-chymotrypsin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM93334(Sul-33)
Affinity DataKd:  3.51E+5nMpH: 7.4Assay Description:Fluorescence titration using alpha-chymotrypsin.More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails ArticlePubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM87059(CHEMBL247767 | Chymostatin)
Affinity DataKi:  8.24E+3nM ΔG°:  -29.0kJ/molepH: 7.6 T: 2°CAssay Description:Chymotrypsin inhibitory activity of compunds was perfomred by the method of Cannel.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM87058(Lignan, 3 | MLS000034632 | N-tert-Butyl-N-(tert-bu...)
Affinity DataKi:  3.18E+4nM ΔG°:  -25.7kJ/molepH: 7.6 T: 2°CAssay Description:Chymotrypsin inhibitory activity of compunds was perfomred by the method of Cannel.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Amherst College

Curated by ChEMBL
LigandPNGBDBM87060(Lignan, 4 | MLS001138823 | N-(4-methylcyclohexyl)-...)
Affinity DataKi:  4.71E+4nM ΔG°:  -24.7kJ/molepH: 7.6 T: 2°CAssay Description:Chymotrypsin inhibitory activity of compunds was perfomred by the method of Cannel.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsinogen A(Bos taurus (bovine))
University Of Alabama At Birmingham

LigandPNGBDBM33260(biguanidine, 2)
Affinity DataKi:  1.35E+6nM ΔG°:  -16.3kJ/molepH: 7.6 T: 2°CAssay Description:All proteases were assayed by monitoring the cleavage of peptide substrate with fluorescent reporter at room temperature with a microtiter plate spec...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetChymotrypsinogen A(Bos taurus (bovine))
University Of Alabama At Birmingham

LigandPNGBDBM222139(Chymostatin | US11859014, Compound chymostatin)
Affinity DataIC50:  5.80E+3nMpH: 7.6Assay Description:The α-chymotrypsin inhibition activity was evaluated in 50 mM Tris-HCl buffer pH 7.6 with 10 mM CaCl2. α-Chymotrypsin (bovine pancreas) at ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsinogen A(Bos taurus (bovine))
University Of Alabama At Birmingham

LigandPNGBDBM50289012(2-(2-Fluoro-phenyl)-benzo[d][1,3]oxazin-4-one | 2-...)
Affinity DataIC50:  6.50E+3nMpH: 7.6Assay Description:The α-chymotrypsin inhibition activity was evaluated in 50 mM Tris-HCl buffer pH 7.6 with 10 mM CaCl2. α-Chymotrypsin (bovine pancreas) at ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsinogen A(Bos taurus (bovine))
University Of Alabama At Birmingham

LigandPNGBDBM50289000(2-(2-Methoxy-phenyl)-benzo[d][1,3]oxazin-4-one | 2...)
Affinity DataIC50:  9.90E+3nMpH: 7.6Assay Description:The α-chymotrypsin inhibition activity was evaluated in 50 mM Tris-HCl buffer pH 7.6 with 10 mM CaCl2. α-Chymotrypsin (bovine pancreas) at ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsinogen A(Bos taurus (bovine))
University Of Alabama At Birmingham

LigandPNGBDBM50077011(2-Phenyl-4H-3,1-benzoxazin-4-one (3) | 2-Phenyl-be...)
Affinity DataIC50:  1.17E+4nMpH: 7.6Assay Description:The α-chymotrypsin inhibition activity was evaluated in 50 mM Tris-HCl buffer pH 7.6 with 10 mM CaCl2. α-Chymotrypsin (bovine pancreas) at ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsinogen A(Bos taurus (bovine))
University Of Alabama At Birmingham

LigandPNGBDBM222117(2-(2-Thienyl)-4H-3,1-benzoxazin-4-one (4) | US1158...)
Affinity DataIC50:  1.21E+4nMpH: 7.6Assay Description:The α-chymotrypsin inhibition activity was evaluated in 50 mM Tris-HCl buffer pH 7.6 with 10 mM CaCl2. α-Chymotrypsin (bovine pancreas) at ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsinogen A(Bos taurus (bovine))
University Of Alabama At Birmingham

LigandPNGBDBM222118(2-(4-Methoxyphenyl)-4H-3,1-benzoxazin-4-one (5))
Affinity DataIC50:  1.44E+4nMpH: 7.6Assay Description:The α-chymotrypsin inhibition activity was evaluated in 50 mM Tris-HCl buffer pH 7.6 with 10 mM CaCl2. α-Chymotrypsin (bovine pancreas) at ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsinogen A(Bos taurus (bovine))
University Of Alabama At Birmingham

LigandPNGBDBM50289006(2-(2-Bromo-phenyl)-benzo[d][1,3]oxazin-4-one | 2-(...)
Affinity DataIC50:  1.88E+4nMpH: 7.6Assay Description:The α-chymotrypsin inhibition activity was evaluated in 50 mM Tris-HCl buffer pH 7.6 with 10 mM CaCl2. α-Chymotrypsin (bovine pancreas) at ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsinogen A(Bos taurus (bovine))
University Of Alabama At Birmingham

LigandPNGBDBM222119(2-(4-Methylphenyl)-4H-3,1-benzoxazin-4-one (7))
Affinity DataIC50:  2.01E+4nMpH: 7.6Assay Description:The α-chymotrypsin inhibition activity was evaluated in 50 mM Tris-HCl buffer pH 7.6 with 10 mM CaCl2. α-Chymotrypsin (bovine pancreas) at ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsinogen A(Bos taurus (bovine))
University Of Alabama At Birmingham

LigandPNGBDBM222120(2-(2,6-Difluorophenyl)-4H-3,1-benzoxazin-4-one (8))
Affinity DataIC50:  2.35E+4nMpH: 7.6Assay Description:The α-chymotrypsin inhibition activity was evaluated in 50 mM Tris-HCl buffer pH 7.6 with 10 mM CaCl2. α-Chymotrypsin (bovine pancreas) at ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetChymotrypsinogen A(Bos taurus (bovine))
University Of Alabama At Birmingham

LigandPNGBDBM33703(2-(2-Nitro-phenyl)-benzo[d][1,3]oxazin-4-one | 2-(...)
Affinity DataIC50:  2.38E+4nMpH: 7.6Assay Description:The α-chymotrypsin inhibition activity was evaluated in 50 mM Tris-HCl buffer pH 7.6 with 10 mM CaCl2. α-Chymotrypsin (bovine pancreas) at ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsinogen A(Bos taurus (bovine))
University Of Alabama At Birmingham

LigandPNGBDBM222121(2-(3-Methylphenyl)-4H-3,1-benzoxazin-4-one (10))
Affinity DataIC50:  2.39E+4nMpH: 7.6Assay Description:The α-chymotrypsin inhibition activity was evaluated in 50 mM Tris-HCl buffer pH 7.6 with 10 mM CaCl2. α-Chymotrypsin (bovine pancreas) at ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsinogen A(Bos taurus (bovine))
University Of Alabama At Birmingham

LigandPNGBDBM222122(2-(2,6-Dimethoxyphenyl)-4H-3,1-benzoxazin-4-one (1...)
Affinity DataIC50:  2.63E+4nMpH: 7.6Assay Description:The α-chymotrypsin inhibition activity was evaluated in 50 mM Tris-HCl buffer pH 7.6 with 10 mM CaCl2. α-Chymotrypsin (bovine pancreas) at ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetChymotrypsinogen A(Bos taurus (bovine))
University Of Alabama At Birmingham

LigandPNGBDBM222123(2-(3-Fluorophenyl)-4H-3,1-benzoxazin-4-one (12))
Affinity DataIC50:  2.82E+4nMpH: 7.6Assay Description:The α-chymotrypsin inhibition activity was evaluated in 50 mM Tris-HCl buffer pH 7.6 with 10 mM CaCl2. α-Chymotrypsin (bovine pancreas) at ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsinogen A(Bos taurus (bovine))
University Of Alabama At Birmingham

LigandPNGBDBM222124(2-(2-Methylphenyl)-4H-3,1-benzoxazin-4-one (13))
Affinity DataIC50:  2.88E+4nMpH: 7.6Assay Description:The α-chymotrypsin inhibition activity was evaluated in 50 mM Tris-HCl buffer pH 7.6 with 10 mM CaCl2. α-Chymotrypsin (bovine pancreas) at ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsinogen A(Bos taurus (bovine))
University Of Alabama At Birmingham

LigandPNGBDBM222125(2-(3-Chlorophenyl)-4H-3,1-benzoxazin-4-one (14))
Affinity DataIC50:  4.18E+4nMpH: 7.6Assay Description:The α-chymotrypsin inhibition activity was evaluated in 50 mM Tris-HCl buffer pH 7.6 with 10 mM CaCl2. α-Chymotrypsin (bovine pancreas) at ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsinogen A(Bos taurus (bovine))
University Of Alabama At Birmingham

LigandPNGBDBM222126(2-(3-Methylphenyl)-7-nitro-4H-3,1-benzoxazin-4-one...)
Affinity DataIC50:  9.41E+4nMpH: 7.6Assay Description:The α-chymotrypsin inhibition activity was evaluated in 50 mM Tris-HCl buffer pH 7.6 with 10 mM CaCl2. α-Chymotrypsin (bovine pancreas) at ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
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