Warning: The NCBI web site requires JavaScript to function. more...
An official website of the United States government
The .gov means it's official. Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you're on a federal government site.
The site is secure. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.
Binding affinity to recombinant human trypsin assessed as increase in fluorescence using H2-OPT as substrate at 1 uM by SDS-PAGE based gel fluorescence scanning analysis
Assay data:3 Tested
SummaryPubMed CitationRelated BioAssays by Target
Inhibition of human Trypsin using Z-Phe-Arg-AMC as substrate incubated for 30 mins by FRET assay
Assay data:1 Tested
Inhibition of human trypsin by fluorescence based analysis
Inhibition of trypsin (unknown origin)
Assay data:2 Tested
Inhibition of human trypsin
Stability of the compound assessed as trypsin (unknown origin)-mediated drug degradation at 100 uM measured after 3 hrs by MALDI-TOF-MS analysis
Assay data:1 Active, 2 Tested
SummaryCompounds, ActivePubMed CitationRelated BioAssays by Target
Inhibition of trypsin (unknown origin) using enzyloxy-carbonyl (Z)-Gly-Pro-Arg-para-nitroanilide as substrate preincubated with compound for 15 mins followed by substrate addition and measured after 15 mins by fluorescence based assay
Stability of compound assessed as trypsin (unknown origin)-mediated compound degradation by measuring parent compound remaining at 150 uM measured upto 4 hrs by RP-HPLC method
Assay data:1 Active, 1 Tested
Covalent inhibition of trypsin (unknown origin) incubated for 1 hr by FRET-based enzymatic assay
Inhibition of trypsin (unknown origin) using Nalpha-benzoyl-D/L-arginine-4-nitroanilide hydrochloride as substrate preincubated for 5 mins followed by substrate addition and measured upto 30 mins by absorbance based assay
Assay data:2 Active, 2 Activity ≤ 1 µM, 6 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed CitationRelated BioAssays by Target
Stability of compound assessed as trypsin (unknown origin) mediated compound degradation by measuring H-O1WO3LFO6O7-OH level measured at 270 mins by LCMS analysis
Stability of compound assessed as trypsin (unknown origin) mediated compound degradation by measuring H-O1WO3LFO6O7-OH level measured at 120 mins by LCMS analysis
Stability of compound assessed as trypsin (unknown origin) mediated compound degradation by measuring H-O1WO3LFO6O7-OH level measured at 60 mins by LCMS analysis
Stability of compound assessed as trypsin (unknown origin) mediated compound degradation by measuring H-O1WO3LFO6O7-OH level measured at 15 mins by LCMS analysis
Stability of compound assessed as trypsin (unknown origin) mediated compound degradation by measuring H-O1WO3LFO6-OH level measured at 270 mins by LCMS analysis
Stability of compound assessed as trypsin (unknown origin) mediated compound degradation by measuring H-O1WO3LFO6-OH level measured at 120 mins by LCMS analysis
Stability of compound assessed as trypsin (unknown origin) mediated compound degradation by measuring H-O1WO3LFO6-OH level measured at 60 mins by LCMS analysis
Stability of compound assessed as trypsin (unknown origin) mediated compound degradation by measuring H-O1WO3LFO6-OH level measured at 15 mins by LCMS analysis
Stability of compound assessed as trypsin (unknown origin) mediated compound degradation by measuring H-O7IGAVLO13VL-NH2 level measured at 270 mins by LCMS analysis
Filters: Manage Filters
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on