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Isolation, synthesis and anti-hepatitis B virus evaluation of p-hydroxyacetophenone derivatives from Artemisia capillaris
被引:24
|作者:
Zhao, Yong
[1
]
Geng, Chang-An
[1
]
Chen, Hao
[1
]
Ma, Yun-Bao
[1
]
Huang, Xiao-Yan
[1
]
Cao, Tuan-Wu
[1
]
He, Kang
[1
]
Wang, Hao
[1
]
Zhang, Xue-Mei
[1
]
Chen, Ji-Jun
[1
]
机构:
[1] Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources West Ch, Kunming 650201, Peoples R China
基金:
美国国家科学基金会;
中国国家自然科学基金;
关键词:
Artemisia capillaris;
p-Hydroxyacetophenone derivatives;
Anti-HBV activity;
Structure-activity relationships;
ANTIVIRAL ACTIVITY;
CONSTITUENTS;
INHIBITORS;
ANALOGS;
ACID;
D O I:
10.1016/j.bmcl.2015.02.024
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
p-Hydroxyacetophenone (p-HAP), as a main hepatoprotective and choleretic constituent of Artemisia capillaris, was revealed with anti-hepatitis B virus (HBV) effects in recent investigation. In addition to p-HAP, four derivatives of p-HAP were also isolated from Artemisia capillaris by various chromatographic methods. Subsequent structural modification on p-HAP and its glycoside led to the synthesis of 28 additional derivatives, of which 13 compounds showed activity inhibiting hepatitis B surface antigen (HBsAg) secretion; and 18 compounds possessed inhibition on HBV DNA replication. The primary structure-activity relationships (SARs) suggested that the conjugated derivatives of p-HAP glycoside and substituted cinnamic acids (2a-2i) obviously enhanced the activity against HBV DNA replication with IC50 values ranged from 5.8 to 74.4 mu M. (C) 2015 Elsevier Ltd. All rights reserved.
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页码:1509 / 1514
页数:6
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