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 in | Carbohydrate research Vol. 360; pp. 47 - 51 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
OXFORD
Elsevier Ltd
01.10.2012
Elsevier |
Subjects | |
Online Access | Get full text |
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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. |
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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 |