石蒜碱
菲咯烷
丙型肝炎病毒
病毒学
寄主(生物学)
行动方式
化学
肝炎病毒
生物
病毒
立体化学
生物碱
生物化学
遗传学
作者
Duozhi Chen,Jie‐Yun Cai,Jun‐Lin Yin,Jian‐Dong Jiang,Chenxu Jing,Yanping Zhu,Junjun Cheng,Ying‐Tong Di,Yu Zhang,Mingming Cao,Shun‐Lin Li,Zong–Gen Peng,Xiao‐Jiang Hao
出处
期刊:Future Medicinal Chemistry
[Newlands Press Ltd]
日期:2015-04-01
卷期号:7 (5): 561-570
被引量:24
摘要
Background: A new series of potential phenanthridine hepatitis C virus (HCV) inhibitors which work by suppressing Hsc70 expression in the host cell was designed and synthesized from lycorine. Results: Thirty-one new potential phenanthridine HCV inhibitors were synthesized and five of these compounds exhibited good anti-HCV activity and these inhibitors probably inhibit HCV by downregulating the host Hsc70 expression. Structure-activity analysis of these compounds revealed that the double bond between C-11 and C-12 and the substituents at C-8 and C-9 are important for their activity against HCV. Conclusion: Suppression of Hsc70 expression in the host cell to limit HCV replication is a potential anti-HCV strategy. Phenanthridines are probably the HCV inhibitors with this mode of action.
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