Anti-HBV active flavone glucosides from Euphorbia humifusa Willd.

Document Type

Article

Publication Date

10-1-2010

Abstract

Thirteen flavone glucosides from the herb of Euphorbia humifusa were isolated and elucidated. Among them, five compounds including apigenin-7-O-β-d-glucopyranoside (2), apigenin-7-O-(6′′-O- galloyl)-β-d-glucopyranoside (3), luteolin-7-O-β-d-glucopyranoside (7), luteolin-7-O-(6′′-O-trans-feruloyl)-β-d-glucopyranoside (8) and luteolin-7-O-(6′′-O-coumaroyl)-β-d-glucopyranoside (9) showed anti-HBV activity in vitro. The structure-activity relationship showed that the parent structure was closely relevant to the anti-HBV activity of these compounds (agigenin > luteolin > quercetin). It was found that the number of glucoside in the structure may significantly influence their activities (flavone monoglucoside > flavone diglucoside) and cytotoxicity (flavone > flavone monoglucoside > flavone diglucoside). In addition, the substitution of acyl group on glucoside may be important to keep the anti-HBV activities of these compounds (galloyl > feruloyl > coumaroyl). © 2010 Elsevier B.V. All rights reserved.

Publication Source (Journal or Book title)

Fitoterapia

First Page

799

Last Page

802

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