Paper
Syntheses and kinetic evaluation of racemic and optically active 2-benzyl-2-methyl-3,4-epoxybutanoic acids as irreversible inactivators for carboxypeptidase A.
Published Apr 1, 2002 · Mijoon Lee, D. H. Kim
Bioorganic & medicinal chemistry
Q2 SJR score
22
Citations
0
Influential Citations
Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
In Vitro StudyStudy Snapshot
The threo-form of 2-benzyl-2-methyl-3,4-epoxybutanoic acid is effective as an inactivator for carboxypeptidase A, but the -methyl group negatively affects inactivation, casting doubt on the presence of the -methyl hole at
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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