Characterisation of new oligoglycosidic compounds in two Chinese medicinal herbs

被引:26
作者
Apers, S
Huang, Y
Van Miert, S
Dommisse, R
Vanden Berghe, D
Pieters, L
Vlietinck, A
机构
[1] Univ Antwerp, Dept Pharmaceut Sci, B-2610 Antwerp, Belgium
[2] Univ Antwerp, Dept Chem, B-2020 Antwerp, Belgium
关键词
quinic acid derivatives; caffeic acid derivatives; flavonoid glycosides; wedelosin; Wedelia chinensis; Kyllinga brevifolia; Compositae; Cyperaceae;
D O I
10.1002/pca.642
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
A series of caffeic acid derivatives (3,5-dicaffeoyl-quinic acid, 3,4-dicaffeoyl-quinic acid, and 4,5-dicaffeoyl-quinic acid), and the new compound beta,3,4-trihydroxyphenethyl-O-[beta-apiofuranosyl-(1-->4)-alpha-rhamnopyranosyl-(1-->3)]-(4-O-caffeoyl)-beta-glucopyranoside (wedelosin), as well as three known flavonoid glycosides (quercetin 3-O-beta-glucoside, kaempferol 3-O-beta-apiosyl-(1-2)-beta-glucoside, and astragalin or kaempferol 3-O-beta-glucoside) were isolated from the Chinese medicinal herb Wedelia chinensis. Wedelosin showed an inhibitory activity on both the classical and the alternative activation pathway of the complement system. Another Chinese medicinal herb, Kyllinga brevifolia, yielded two known flavonoid glycosides [kaempferol 3-O-beta-apiosyl-(1-2)-beta-glucoside and isorhamnetin 3-O-beta-apiosyl-(1-2)-beta-glucoside], and a new quercetin triglycoside [quercetin 3-O-beta-apiofuranosyl-(1-->2)-beta-glucopyranoside 7-O-alpha-rhamnopyranoside]. The latter compound showed a moderate anti-viral activity. Copyright (C) 2002 John Wiley Sons, Ltd.
引用
收藏
页码:202 / 206
页数:5
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