Study on 2-arylthio-5-iodo pyrimidine derivatives as novel nonnucleoside inhibitors against hepatitis B virus DNA replication

被引:3
作者
Zhao, Jianxiong [1 ]
Tu, Jing [2 ,3 ]
Fan, Ningning [1 ]
Chen, Xiangmei [2 ,3 ]
Lu, Fengmin [2 ,3 ]
Zhang, Yu [1 ]
Zhang, Liang [1 ]
Tian, Chao [1 ]
Zhang, Zhili [1 ]
Liu, Junyi [1 ,4 ]
Wang, Xiaowei [1 ]
机构
[1] Peking Univ, Sch Pharmaceut Sci, Dept Chem Biol, Beijing 100191, Peoples R China
[2] Peking Univ, Sch Basic Med Sci, Dept Microbiol, Beijing 100191, Peoples R China
[3] Peking Univ, Sch Basic Med Sci, Ctr Infect Dis, Beijing 100191, Peoples R China
[4] Peking Univ, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China
基金
中国国家自然科学基金;
关键词
DNA replication; dose-response relationship; HBeAg; HBsAg; HBV DNA polymerase; hepatitis B Virus; nonnucleoside inhibitors; pharmacophore models; pregenome RNA; pyrimidine derivatives; REVERSE-TRANSCRIPTASE; BIOLOGICAL EVALUATION; ANTIVIRAL ACTIVITY; HBV; IDENTIFICATION; COMPOUND; PREVENTION; CELLS;
D O I
10.4155/fmc.16.13
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: Novel nonnucleoside hepatitis B virus inhibitors have been recently developed for the reason of drug-resistant mutations and adverse effects of nucleoside analogs. In this study, two series of 2-arylthio-5-iodo pyrimidine analogs were firstly reported as potential anti-HBV agents. Methodology: Target compounds were prepared according to two high-yielded synthetic routes, and their anti-HBV activities were evaluated on Hep2.2.15 and HepAD38 cell lines, respectively. To probe the mechanism of active agents, a cell-based (Huh-7) study of biochemical markers (e.g., HBeAg, HBsAg, intracellular HBV DNA and pgRNA) was performed. Furthermore, the pharmacophore models were constructed for future optimization of lead compounds. Conclusion: 2-Arylthio-5-iodo pyrimidine derivatives firstly proved to be effective against HBV, which paves the way for future development of nonnucleoside anti-HBV agents.
引用
收藏
页码:751 / 763
页数:13
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