4.7 Review

What is holding back the development of antiviral metallodrugs? A literature overview and implications for SARS-CoV-2 therapeutics and future viral outbreaks

期刊

DALTON TRANSACTIONS
卷 49, 期 45, 页码 16004-16033

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0dt02478c

关键词

-

资金

  1. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES) - Brasil - Prevention and Combat of Outbreaks, Endemics, Epidemics and Pandemics [88881.506794/2020-01]
  2. Royal Society - Newton Advanced Fellowship [NA 150195]
  3. FAPEMIG (Minas Gerais Research Foundation) [APQ-00587-14, SICONV 793988/2013, APQ-03385-18]
  4. Sao Paulo Research Foundation (FAPESP) [2018/21537-6]
  5. FAPESP [2018/12062-4]
  6. CAPES [001]
  7. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [18/12062-4] Funding Source: FAPESP

向作者/读者索取更多资源

In light of the Covid-19 outbreak, this review brings together historical and current literature efforts towards the development of antiviral metallodrugs. Classical compounds such as CTC-96 and auranofin are discussed in depth, as pillars for future metallodrug development. From the recent literature, both cell-based results and biophysical assays against potential viral biomolecule targets are summarized here. The comprehension of the biomolecular targets and their interactions with coordination compounds are emphasized as fundamental strategies that will foment further development of metal-based antivirals. We also discuss other possible and unexplored methods for unveiling metallodrug interactions with biomolecules related to viral replication and highlight the specific challenges involved in the development of antiviral metallodrugs.

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

4.7
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