| Literature DB >> 25737008 |
Yong Zhao1, Chang-An Geng1, Hao Chen1, Yun-Bao Ma1, Xiao-Yan Huang1, Tuan-Wu Cao1, Kang He1, Hao Wang1, Xue-Mei Zhang1, Ji-Jun Chen2.
Abstract
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 A. 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 μM.Entities:
Keywords: Anti-HBV activity; Artemisia capillaris; Structure–activity relationships; p-Hydroxyacetophenone derivatives
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Year: 2015 PMID: 25737008 DOI: 10.1016/j.bmcl.2015.02.024
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823