Anti-SARS-CoV-2 Potential of Artemisinins In Vitro

被引:106
|
作者
Cao, Ruiyuan [1 ]
Hu, Hengrui [2 ,3 ]
Li, Yufeng [2 ,3 ]
Wang, Xi [2 ]
Xu, Mingyue [2 ,3 ]
Liu, Jia [2 ]
Zhang, Huanyu [2 ,3 ]
Yan, Yunzheng [1 ]
Zhao, Lei [1 ]
Li, Wei [1 ]
Zhang, Tianhong [1 ,4 ]
Xiao, Dian [1 ]
Guo, Xiaojia [1 ]
Li, Yuexiang [1 ]
Yang, Jingjing [1 ]
Hu, Zhihong [2 ]
Wang, Manli [2 ]
Zhong, Wu [1 ]
机构
[1] Beijing Inst Pharmacol & Toxicol, Natl Engn Res Ctr Emergency Drug, Beijing 100850, Peoples R China
[2] Chinese Acad Sci, Ctr Biosafety Megasci, Wuhan Inst Virol, State Key Lab Virol, Wuhan 430071, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Guoke Excellence Beijing Med Technol Res Co Ltd, Beijing 100176, Peoples R China
来源
ACS INFECTIOUS DISEASES | 2020年 / 6卷 / 09期
关键词
artemisinin; SARS-CoV-2; COVID-19; antiviral drug; drug repurposing; HUMAN CYTOMEGALOVIRUS; ANTIVIRAL ACTIVITY; ARTESUNATE;
D O I
10.1021/acsinfecdis.0c00522
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The discovery of novel drug candidates with anti-severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) potential is critical for the control of the global COVID-19 pandemic. Artemisinin, an old antimalarial drug derived from Chinese herbs, has saved millions of lives. Artemisinins are a cluster of artemisinin-related drugs developed for the treatment of malaria and have been reported to have multiple pharmacological activities, including anticancer, antiviral, and immune modulation. Considering the reported broad-spectrum antiviral potential of artemisinins, researchers are interested in whether they could be used to combat COVID-19. We systematically evaluated the anti-SARS-CoV-2 activities of nine artemisinin-related compounds in vitro and carried out a time-of-drug-addition assay to explore their antiviral mode of action. Finally, a pharmacokinetic prediction model was established to predict the therapeutic potential of selected compounds against COVID-19. Arteannuin B showed the highest antiSARS-CoV-2 potential with an EC50 of 10.28 +/- 1.12 mu M. Artesunate and dihydroartemisinin showed similar EC50 values of 12.98 +/- 5.30 mu M and 13.31 +/- 1.24 mu M, respectively, which could be clinically achieved in plasma after intravenous administration. Interestingly, although an EC50 of 23.17 +/- 3.22 mu M was not prominent among the tested compounds, lumefantrine showed therapeutic promise due to high plasma and lung drug concentrations after multiple dosing. Further mode of action analysis revealed that arteannuin B and lumefantrine acted at the post-entry step of SARS-CoV-2 infection. This research highlights the anti-SARS-CoV-2 potential of artemisinins and provides leading candidates for anti-SARS-CoV-2 drug research and development.
引用
收藏
页码:2524 / 2531
页数:8
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