Anthraquinone glycosides from Cassia roxburghii and evaluation of its free radical scavenging activity

Two new anthraquinone glycosides, namely emodin 1-O-β-glucoside (2→1) glucopyranoside (1) and aloemodin 8-O-β-glucoside (6→1) glucopyranoside (2) have been isolated from Cassia roxburghii. [Display omitted] ► Two new anthraquinone glycosides. ► NMR of the isolated compounds. ►Free radicals scavengin...

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Published inCarbohydrate research Vol. 360; pp. 47 - 51
Main Authors El-Toumy, Sayed A., El Souda, Sahar S., Mohamed, Tahia K., Brouard, Iñaki, Bermejo, Jame
Format Journal Article
LanguageEnglish
Published OXFORD Elsevier Ltd 01.10.2012
Elsevier
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Summary:Two new anthraquinone glycosides, namely emodin 1-O-β-glucoside (2→1) glucopyranoside (1) and aloemodin 8-O-β-glucoside (6→1) glucopyranoside (2) have been isolated from Cassia roxburghii. [Display omitted] ► Two new anthraquinone glycosides. ► NMR of the isolated compounds. ►Free radicals scavenging activity. The methanolic extract of the leaves of Cassia roxburghii DC., was investigated for its anthraquinone glycosides and antioxidant activity. Two new anthraquinone glycosides named emodin 1-O-β-d-glucopyranosyl-(1→2)-glucopyranoside (1) and aloemodin 8-O-β-d-glucopyranosyl-(1→6)-glucopyranoside (2) along with aloemodin 8-O-β-d-glucopyranoside (3), emodin (4), aloemodin (5) and one flavonoid, quercetin-3-O-α-l-rhamnopyranoside, were isolated from the leaves of C. roxburghii. Structures of the isolated compounds were established by UV, HRESI-MS, and 1D/2D 1H/13C NMR spectroscopy. The total extract and some isolated compounds were determined against DPPH (2,2-diphenyl-1-(2,4,6-trinitrophenyl)hydrazinyl radical, for their free radical scavenging activity, the total alcoholic extract showed strong antioxidant activity while the two new compounds showed weak antioxidant activity.
Bibliography:http://dx.doi.org/10.1016/j.carres.2012.07.020
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0008-6215
1873-426X
DOI:10.1016/j.carres.2012.07.020