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A new flavonol glycoside from the medicinal halophyte Suaeda fruticosa

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Version 2 2014-06-30, 08:43
Version 1 2014-06-30, 08:43
journal contribution
posted on 2014-06-30, 08:43 authored by Samia Oueslati, Riadh Ksouri, André Pichette, Serge Lavoie, Karl Girard-Lalancette, Vakhtang Mshvildadze, Chedly Abdelly, Jean Legault

A new flavonol glycoside, namely 3-(α-rhamnopyranosyl-(1 → 2)-[β-xylopyranosyl-(1 → 6)]-β-glucopyranosyloxy) isorhamnetin was reported from methanol extracts of aerial parts of Suaeda fruticosa for the first time. In this work, liquid chromatography coupled to atmospheric pressure chemical ionisation mass spectrometry, high-resolution mass spectrometry and nuclear magnetic resonance spectroscopy were used to identify this new compound. Structure was elucidated on the basis of extensive spectroscopic analysis, including HSQC, HMBC and 1H–1H COSY. Antioxidant potentialities of a pure compound were evaluated. The estimation of antioxidant capacities using oxygen radical absorbance capacity (ORAC method) and a cell based-assay (WS1) indicated that this new flavonol exhibited the highest antioxidant activities with an ORAC value of 5.0 ± 0.3 μmol Trolox/μmol and inhibited the tBH-induced oxidation of 2′,7′-dichlorofluorescin with an IC50 value of 4.9 ± 0.6 μM.

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