Journal of Agricultural and Food Chemistry · 1999 · 163 citations · 24 references
Life SciencesBiochemistryPlant BiologyFood ChemistryGreen ChemistryPlant BiochemistryAntioxidant DefenseFood AntioxidantsLipid MetabolismLipid OxidationLipid PeroxidationAntioxidant InhibitionAntioxidant MetabolitesAntioxidant Natural ProductsAntioxidants In LipidsIron-dependent Lipid PeroxidationNatural AntioxidantsPlant Extract AntioxidantsProoxidant Effects
Montmorency and Balaton tart cherries were lyophilized and sequentially extracted with hexane, ethyl acetate, and methanol. Methanolic extracts of dried Balaton and Montmorency tart cherries (Prunus cerasus) inhibited lipid peroxidation induced by Fe(2+) at 25 ppm concentrations. Further partitioning of this methanol extract with EtOAc yielded a fraction that inhibited lipid peroxidation by 76% at 25 ppm. Purification of this EtOAc fraction afforded eight polyphenolic compounds, 5,7,4'-trihydroxyflavanone (1), 5,7, 4'-trihydroxyisoflavone (2), chlorogenic acid (3), 5,7,3', 4'-tetrahydroxyflavonol-3-rhamnoside (4), 5,7,4'-trihydroxyflavonol 3-rutinoside (5), 5,7,4'-trihydroxy-3'methoxyflavonol-3-rutinoside (6), 5,7,4'-trihydroxyisoflavone-7-glucoside (7), and 6, 7-dimethoxy-5,8,4'-trihydroxyflavone (8), as characterized by (1)H and (13)C NMR experiments. The antioxidant assays revealed that 7-dimethoxy-5,8,4'-trihydroxyflavone (8) is the most active, followed by quercetin 3-rhamnoside, genistein, chlorogenic acid, naringenin, and genistin, at 10 microM concentrations.
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Carbon-13 NMR studies of flavonoids—III
K. R. Markham, B. Ternai, Roger Stanley et al. · Tetrahedron · 1978 · 876 citations
Pawan K. Agrawal · 1989 · 864 citations