Chemical Constituents of Saniculiphyllum guangxiense

被引:10
|
作者
Geng, Chang-An [1 ]
Huang, Xiao-Yan [1 ]
Lei, Li-Gong [2 ]
Zhang, Xue-Mei [1 ]
Chen, Ji-Jun [1 ]
机构
[1] Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources W China, Heilongtan 650201, Kunming, Peoples R China
[2] Chinese Acad Sci, Kunming Inst Bot, Key Lab Biodivers & Biogeog, Heilongtan 650201, Kunming, Peoples R China
基金
中国国家自然科学基金;
关键词
Saniculiphyllum guangxiense; Nitrile glucosides; Triterpenoids; Glucosides; Antiviral activity; X-Ray crystallography; PENTACYCLIC TRITERPENOIDS; GLYCOSIDES;
D O I
10.1002/cbdv.201100270
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
The first phytochemical investigation on Saniculiphyllum guangxiense resulted in the isolation of two new triterpenoids, 16 beta-hydroxybryodulcosigenin (3) and 3a-O-feruloylolean-12-en-27-oic acid (6), together with six known compounds, menisdaurin (1), purshianin (2), oleanolic acid (4), 3 beta-hydroxyolean-12-en-27-oic acid (5), beta-sitosterol (7), and daucosterol (8), which were characterized by extensive spectroscopic analyses and in one case by X-ray diffraction. According to this primary investigation, S. guangxiense is rich in nitrile glucosides and triterpenoids, of which menisdaurin (1; 0.06%) and purshianin (2; 0.015%) are the main constituents. Compounds 16 were assayed for their anti-hepatitis B virus (HBV) activities against the secretion of HBsAg and HBeAg, as well as HBV DNA replication on Hep G 2.2.15 cell line in vitro. The most active compound, menisdaurin (1), inhibits HBV DNA replication with an IC50 value of 0.32 mM (SI>11.97).
引用
收藏
页码:1508 / 1516
页数:9
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