4.1 Review

Antiviral nucleoside analogs

期刊

CHEMISTRY OF HETEROCYCLIC COMPOUNDS
卷 57, 期 4, 页码 326-341

出版社

SPRINGER
DOI: 10.1007/s10593-021-02912-8

关键词

nucleoside analogs; pronucleotides; antiviral activity

资金

  1. Russian Science Foundation [19-13-00003]
  2. Russian Science Foundation [19-13-00003] Funding Source: Russian Science Foundation

向作者/读者索取更多资源

The minireview discusses the modification of native nucleosides leading to the synthesis of diverse nucleoside analog libraries. It focuses on prodrug forms and antiviral cyclic nucleoside analogs, listing approved drugs for HIV, hepatitis B, C, and influenza, as well as those in clinical trials. It also mentions nucleoside analogs inhibiting the replication of SARS-CoV and MERS-CoV, including remdesivir used in the fight against COVID-19.
The minireview surveys the modification of native nucleosides as a result of which huge libraries of nucleoside analogs of various structures were synthesized. Particular attention is paid to the synthesis of the so-called prodrug forms of nucleoside analogs which ensure their penetration into the cell and metabolism to active 5'-triphosphate derivatives. All the best known antiviral cyclic nucleoside analogs approved for the treatment of HIV infections, hepatitis B, C, and influenza since the 1960s, as well as those in various stages of clinical trials in recent years, are listed. Nucleoside analogs that have shown the ability to inhibit the replication of SARS-CoV and MERS-CoV are discussed, including remdesivir, approved by the FDA for emergency use in the fight against COVID-19.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.1
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据