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Identification of existing pharmaceuticals and herbal medicines as inhibitors of SARS-CoV-2 infection
Author(s) -
Jia Tsrong Jan,
Ting-Jen Rachel Cheng,
Yu-Pu Juang,
Hsiu Hua,
YingTa Wu,
Wen Bin Yang,
Cheng-Wei Cheng,
Hong Chen,
Ting Hung Chou,
JiunJie Shie,
Wei Cheng,
RongJie Chein,
ShiShan Mao,
PiHui Liang,
Che Ma,
Shang Cheng Hung,
Chi Huey Wong
Publication year - 2021
Publication title -
proceedings of the national academy of sciences of the united states of america
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.2021579118
Subject(s) - virology , pharmacology , nelfinavir , medicine , traditional medicine , virus , biology , viral load , antiretroviral therapy
The outbreak of COVID-19 caused by SARS-CoV-2 has resulted in more than 50 million confirmed cases and over 1 million deaths worldwide as of November 2020. Currently, there are no effective antivirals approved by the Food and Drug Administration to contain this pandemic except the antiviral agent remdesivir. In addition, the trimeric spike protein on the viral surface is highly glycosylated and almost 200,000 variants with mutations at more than 1,000 positions in its 1,273 amino acid sequence were reported, posing a major challenge in the development of antibodies and vaccines. It is therefore urgently needed to have alternative and timely treatments for the disease. In this study, we used a cell-based infection assay to screen more than 3,000 agents used in humans and animals, including 2,855 small molecules and 190 traditional herbal medicines, and identified 15 active small molecules in concentrations ranging from 0.1 nM to 50 μM. Two enzymatic assays, along with molecular modeling, were then developed to confirm those targeting the virus 3CL protease and the RNA-dependent RNA polymerase. Several water extracts of herbal medicines were active in the cell-based assay and could be further developed as plant-derived anti-SARS-CoV-2 agents. Some of the active compounds identified in the screen were further tested in vivo, and it was found that mefloquine, nelfinavir, and extracts of Ganoderma lucidum (RF3), Perilla frutescens , and Mentha haplocalyx were effective in a challenge study using hamsters as disease model.

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