4.7 Article

Defending Antiviral Cationic Amphiphilic Drugs That May Cause Drug-Induced Phospholipidosis

期刊

JOURNAL OF CHEMICAL INFORMATION AND MODELING
卷 61, 期 9, 页码 4125-4130

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jcim.1c00903

关键词

-

资金

  1. NIH from NIGMS [R44GM122196-02A1]
  2. NCCAM [3R43AT010585-01S1]
  3. NIEHS [1R43ES031038-01]

向作者/读者索取更多资源

While a recent publication suggested that cationic amphiphilic drugs repurposed for COVID-19 may not be effective in vivo, additional experimental data supports the efficacy of many of these molecules both in vitro and in vivo without causing phospholipidosis. Therefore, further exploration of this class of compounds is warranted in the search for broad spectrum antivirals.
A recent publication in Science has proposed that cationic amphiphilic drugs repurposed for COVID-19 typically use phosholipidosis as their antiviral mechanism of action in cells but will have no in vivo efficacy. On the contrary, our viewpoint, supported by additional experimental data for similar cationic amphiphilic drugs, indicates that many of these molecules have both in vitro and in vivo efficacy with no reported phospholipidosis, and therefore, this class of compounds should not be avoided but further explored, as we continue the search for broad spectrum antivirals.

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