A novel flavonoid glucloside from Anoectochilus roxburghii (Wall.) Lindl.

被引:22
|
作者
He, CN
Wang, CL
Guo, SX [1 ]
Yang, JS
Xiao, PG
机构
[1] Chinese Acad Med Sci, Inst Med Plant Dev, Beijing 100094, Peoples R China
[2] Peking Union Med Coll, Beijing 100094, Peoples R China
关键词
Anoectochilus roxburghii; quercetin-7-O-beta-D-[6"-O-(trans-feruloyl)]-glucopyranoside; radical-scavenging activity;
D O I
10.1111/j.1744-7909.2006.00179.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Eight compounds were isolated from the ethyl acetate- and n-butanol-soluble fractions of the ethanolic extract of the whole plant of Anoectochilus roxburghii (Wall.) Lindl. (Orchidaceae). On the basis of spectroscopic methods, the structures of these compounds were elucidated as quercetin-7-O-beta-D-[6"-O-(trans-feruloyl)]-glucopyranoside (compound 1), 8-C-p-Hydroxybenzylquercetin (compound 2), isorhamnetin-7-O-beta-D-glucopyranoside (compound 3), isorhamnetin-3-O-beta-D-glucopyranoside (compound 4), kaempferol-3-O-beta-D-glucopyranoside (compound 5), kaempferol-7-O-beta-D-glucopyranoside (compound 6), 5-hydroxy-3',4',7-trimethoxyflavonol-3-O-beta-D-rutinoside (compound 7), and isorhamnetin-3-O-beta-D-rutinoside (compound 8). Of the compounds isolated, compound 1 was a new flavonoid glucoside and exhibited strong scavenging activity against the 1,1-diphenyl-2-picrylhydrazyl free radical, whereas the ethanolic extract showed weak activity. Compounds 2-8 were obtained from this family for the first time.
引用
收藏
页码:359 / 363
页数:5
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