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Chymotrypsin Serine protease panel
Assay data:1 Tested
SummaryRelated BioAssays by Target
Binding affinity to recombinant human chymotrypsin assessed as increase in fluorescence using H2-OPT as substrate at 1 uM by SDS-PAGE based gel fluorescence scanning analysis
Assay data:3 Active, 6 Tested
Inactivation of bovine alpha-chymotrypsin assessed as Ki/KI ratio
Inactivation of bovine alpha-chymotrypsin assessed as Ki/KI ratio at pH 7.5
Inhibition of bovine alpha-chymotrypsin at 500 uM by chromogenic substrate hydrolysis assay
Assay data:27 Tested
Stability of the compound assessed as chymotrypsin (unknown origin)-mediated drug degradation at 100 uM measured after 3 hrs by MALDI-TOF-MS analysis
Assay data:1 Active, 1 Tested
Stability of the compound assessed as chymotrypsin (unknown origin)-mediated drug degradation by measuring residual ratio at 100 uM measured after 1 hr by MALDI-TOF-MS analysis
Stability of the compound assessed as chymotrypsin (unknown origin)-mediated drug degradation by measuring cleavage at Leu21-Arg22 residue at 100 uM measured for 3 hrs by MALDI-TOF-MS analysis
Stability of the compound assessed as chymotrypsin (unknown origin)-mediated drug degradation by measuring cleavage at Tyr7-Ser8 residue at 100 uM measured for 3 hrs by MALDI-TOF-MS analysis
Selectivity interaction (Serine protease panel) EUB0000735a CTRC
Inhibition of human pancreas chymotrypsin at 100 uM using Suc-Ala-Ala-Pro-Phe-AMC as substrate preincubated for 15 mins incubated followed by addition of substrate measured after 60 mins by measuring amount of AMC formed by spectrofluorimetric method
SummaryPubMed CitationRelated BioAssays by Target
Inhibition of human pancreas chymotrypsin using Suc-Ala-Ala-Pro-Phe-AMC as substrate preincubated for 15 mins incubated followed by addition of substrate measured after 60 mins by measuring amount of AMC formed by spectrofluorimetric method
Inhibition of human Chymotrypsin at 20 uM using Suc-Ala-Ala-Pro-Phe-NHMec as fluorogenic substrate preincubated for 15 mins followed by substrate addition by spectrophotometry analysis
Binding affinity to human chymotrypsin assessed as inhibition constant using 3-Carbomethoxypropionyl-L-arginyl-Lprolyl-L-tyrosine p-Nitroaniline as substrate measured upto 120 mins by spectrophotometric analysis
Assay data:1 Active, 1 Activity ≤ 1 µM, 1 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed CitationRelated BioAssays by Target
Stability of the compound in PBS at pH 7.4 assessed as chymotrypsin (unknown origin)-mediated proteolysis by measuring remaining compound after 12 hrs by HPLC analysis
Assay data:2 Tested
Chromogenic Enzyme Activity Assays from US Patent US11149067: "Tailored cyclodepsipeptides as potent non-covalent serine protease inhibitors"
Assay data:31 Active, 19 Activity ≤ 1 µM, 33 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMRelated BioAssays by Target
Proteasome-Activity Inhibitory Assay from US Patent US10640533: "Epoxyketone compounds for enzyme inhibition"
Assay data:18 Active, 2 Activity ≤ 1 nM, 19 Activity ≤ 1 µM, 19 Tested
α-Chymotrypsin Inhibition Kinetic Assay from Article 10.1016/j.bioorg.2017.01.001: "Synthesis, structure-activity relationships studies of benzoxazinone derivatives as a-chymotrypsin inhibitors."
Assay data:6 Active, 19 Tested
SummaryCompounds, ActivePubMed CitationRelated BioAssays by DepositorRelated BioAssays by Target
α-Chymotrypsin Inhibition Assay from Article 10.1016/j.bioorg.2017.01.001: "Synthesis, structure-activity relationships studies of benzoxazinone derivatives as a-chymotrypsin inhibitors."
Assay data:3 Active, 30 Tested
Fluorescence Assay from Article 10.1021/cc700189b: "Diversity-oriented fluorescence library approach (DOFLA) to the discovery of chymotrypsin sensor."
Assay data:7 Tested
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