Methods of Synthesis of Remdesivir, Favipiravir, Hydroxychloroquine, and Chloroquine: Four Small Molecules Repurposed for Clinical Trials during the Covid-19 Pandemic

被引:21
作者
Al Bujuq, Nader [1 ]
机构
[1] Taibah Univ, Fac Sci, Chem Dept, Medina, Saudi Arabia
来源
SYNTHESIS-STUTTGART | 2020年 / 52卷 / 24期
关键词
COVID-19; chloroquine; favipiravir; remdesivir; hydroxychloroquine; synthesis; antiviral; MAJOR METABOLITES; T-705; FAVIPIRAVIR; PROTEIN-BINDING; EBOLA-VIRUS; ENANTIOMERS; DESETHYLCHLOROQUINE; INHIBITORS; AMINATION; MECHANISM; DISCOVERY;
D O I
10.1055/s-0040-1707386
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The novel coronavirus (COVID-19) disease has rapidly evolved into a sweeping pandemic despite public health measures. Screening and development of new vaccines and antivirals are expensive and time consuming. However, the repositioning of available drugs is an essential and universal strategy in the development of new drugs and therefore should receive priority attention as well as international government and agency support. Significant drugs such as chloroquine, hydroxychloroquine, favipiravir and remdesivir, are currently undergoing clinical studies to test their efficacy and safety. Some promising results have been achieved thus far in the treatment of COVID-19. In this article we summarize and discuss the most common synthetic strategies to apply in the preparation of these drug molecules. It is hoped that this compendium will provide an accessible useful guide and reference source for scientists, researchers and academia in their battle against COVD-19.
引用
收藏
页码:3735 / 3750
页数:16
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