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Structure and Physiological Activity of Phenyl Propanoid Glycosides in Lemon (<i>Citrus limon</i>B<scp>urm</scp>.<i>f</i>.) Peel
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1991
Year
Hot WaterLemon PeelBiochemistryMedicineGlycobiologyPhytopharmacologyPhytochemicalPhytochemistryPharmacologyPhysiological ActivityPhenyl Propanoid Glycosides
We report here the difference between phenyl propanoid glycosides obtained from hot water and methanol extracts of lemon peel. Eight phenyl propanoid glycosides were isolated, and their structures were established by UV, MS, 1H-NMR and 13C-NMR spectroscopy, as well as by chemical evidence. They were coniferin (1), syringin (2), dehydrodiconiferyl alcohol-4-β-glucoside (3), citrusin A (4), citrusin B (5), citrusin C (6), methyl-3-(4-β-glucopyranosyl-3-methoxyphenyl)propionate (7) and methyl-3-{4-(6-O-α-glucopyranosyl-β-glucopyranosyl)-3-hydroxyphenyl}propionate (8). Compound 7, after intravenously injecting (0.5 mg/100 g of body weight) into stroke-prone spontaneously hypotensive rats (SHR-SP), was found to lower the blood pressure. Among these isolated compounds, 7 and 8 are new phenyl propanoid glycosides.