Journal of Agricultural and Food Chemistry · 2002 · 280 citations · 19 references
Life SciencesBiochemistryFood ScienceEthnobotanyFood ChemistryPlant BiochemistryBioactive Food ComponentsMedicinal PlantsPhenolic Compound AnalysisActive Compound IsolationBioactive Plant CompoundsChromatographic Analysis Of PhenolicsFree Radical ScavengingPhenolic CompoundsPhenolic Content AnalysisPlant Extract AntioxidantsPlant-derived Natural Products
Nine phenolic compounds were isolated from the ethyl acetate and n-butanol fractions of almond (Prunus amygdalus) skins. On the basis of NMR data, MS data, and comparison with the literature, these compounds were identified as 3'-O-methylquercetin 3-O-beta-D-glucopyranoside (1); 3'-O-methylquercetin 3-O-beta-D-galactopyranoside (2); 3'-O-methylquercetin 3-O-alpha-L-rhamnopyranosyl-(1-->6)-beta-D-glucopyranoside (3); kaempferol 3-O-alpha-L-rhamnopyranosyl-(1-->6)-beta-D-glucopyranoside (4); naringenin 7-O-beta-D-glucopyranoside (5); catechin (6); protocatechuic acid (7); vanillic acid (8); and p-hydroxybenzoic acid (9). All of these compounds have been isolated from almond skins for the first time. 2,2-Diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging activities for compounds 1-9 were determined. Compounds 6 and 7 show very strong DPPH radical scavenging activity. Compounds 1-3, 5, 8, and 9 show strong activity, whereas compound 4 has very weak activity.
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The flavonoids advances in research since 1986:
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