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- Achour, Lotfi, et al. Show all 9 Authors
- Applied biochemistry and biotechnology 2019 v.187 no.3 pp. 1113-1130
- acarbose; active ingredients; acute toxicity; alkenes; alpha-amylase; animals; anti-infective agents; antimicrobial properties; antioxidant activity; antioxidants; bleaching; cell proliferation; computer simulation; cycloaddition reactions; cytotoxicity; death; drugs; enantiomers; enzyme inhibition; human cell lines; inhibitory concentration 50; lipid peroxidation; median effective concentration; thiobarbituric acid-reactive substances
- ... A series of enantiopure isoxazolidines (3a–c) were synthesized by 1,3-dipolar cycloaddition between a (−)-menthone-derived nitrone and various terminal alkenes. The screened compounds were evaluated for their antioxidant activity by two in vitro antioxidant assays, including β-carotene/linoleic acid bleaching, and inhibition of lipid peroxidation (thiobarbituric acid reactive species, TBARS). The ...