Identification of existing pharmaceuticals and herbal medicines as inhibitors of SARS-CoV-2 infection

被引:145
作者
Jan, Jia-Tsrong [1 ]
Cheng, Ting-Jen Rachel [1 ]
Juang, Yu-Pu [2 ]
Ma, Hsiu-Hua [1 ]
Wu, Ying-Ta [1 ]
Yang, Wen-Bin [1 ]
Cheng, Cheng-Wei [1 ]
Chen, Xiaorui [1 ]
Chou, Ting-Hung [3 ]
Shie, Jiun-Jie [3 ]
Cheng, Wei-Chieh [1 ]
Chein, Rong-Jie [3 ]
Mao, Shi-Shan [1 ]
Liang, Pi-Hui [1 ,2 ]
Ma, Che [1 ]
Hung, Shang-Cheng [1 ]
Wong, Chi-Huey [1 ,4 ]
机构
[1] Acad Sinica, Genom Res Ctr, Taipei 115, Taiwan
[2] Natl Taiwan Univ, Sch Pharm, Taipei 110, Taiwan
[3] Acad Sinica, Inst Chem, Taipei 128, Taiwan
[4] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
关键词
SARS-CoV-2; drug repurposing; antiviral; cell-based and animal studies; PROTEASE; CORONAVIRUS; REPLICATION; CHANNELS; ACE2;
D O I
10.1073/pnas.2021579118
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 mu M. 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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相关论文
共 60 条
[1]   Prioritization of Anti-SARS-Cov-2 Drug Repurposing Opportunities Based on Plasma and Target Site Concentrations Derived from their Established Human Pharmacokinetics [J].
Arshad, Usman ;
Pertinez, Henry ;
Box, Helen ;
Tatham, Lee ;
Rajoli, Rajith K. R. ;
Curley, Paul ;
Neary, Megan ;
Sharp, Joanne ;
Liptrott, Neill J. ;
Valentijn, Anthony ;
David, Christopher ;
Rannard, Steve P. ;
O'Neill, Paul M. ;
Aljayyoussi, Ghaith ;
Pennington, Shaun H. ;
Ward, Stephen A. ;
Hill, Andrew ;
Back, David J. ;
Khoo, Saye H. ;
Bray, Patrick G. ;
Biagini, Giancarlo A. ;
Owen, Andrew .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2020, 108 (04) :775-790
[2]   Cepharanthine: An update of its mode of action, pharmacological properties and medical applications [J].
Bailly, Christian .
PHYTOMEDICINE, 2019, 62
[3]   Carnosic acid [J].
Birtic, Simona ;
Dussort, Pierre ;
Pierre, Francois-Xavier ;
Bily, Antoine C. ;
Roller, Marc .
PHYTOCHEMISTRY, 2015, 115 :9-19
[4]   The Global Phosphorylation Landscape of SARS-CoV-2 Infection [J].
Bouhaddou, Mehdi ;
Memon, Danish ;
Meyer, Bjoern ;
White, Kris M. ;
Rezelj, Veronica V. ;
Marrero, Miguel Correa ;
Polacco, Benjamin J. ;
Melnyk, James E. ;
Ulferts, Svenja ;
Kaake, Robyn M. ;
Batra, Jyoti ;
Richards, Alicia L. ;
Stevenson, Erica ;
Gordon, David E. ;
Rojc, Ajda ;
Obernier, Kirsten ;
Fabius, Jacqueline M. ;
Soucheray, Margaret ;
Miorin, Lisa ;
Moreno, Elena ;
Koh, Cassandra ;
Quang Dinh Tran ;
Hardy, Alexandra ;
Robinot, Remy ;
Vallet, Thomas ;
Nilsson-Payant, Benjamin E. ;
Hernandez-Armenta, Claudia ;
Dunham, Alistair ;
Weigang, Sebastian ;
Knerr, Julian ;
Modak, Maya ;
Quintero, Diego ;
Zhou, Yuan ;
Dugourd, Aurelien ;
Valdeolivas, Alberto ;
Patil, Trupti ;
Li, Qiongyu ;
Huttenhain, Ruth ;
Cakir, Merve ;
Muralidharan, Monita ;
Kim, Minkyu ;
Jang, Gwendolyn ;
Tutuncuoglu, Beril ;
Hiatt, Joseph ;
Guo, Jeffrey Z. ;
Xu, Jiewei ;
Bouhaddou, Sophia ;
Mathy, Christopher J. P. ;
Gaulton, Anna ;
Manners, Emma J. .
CELL, 2020, 182 (03) :685-+
[5]  
Cao B, 2020, NEW ENGL J MED, V382, P1787, DOI [10.1056/NEJMoa2001282, 10.1056/NEJMc2008043]
[6]   Beyond Shielding: The Roles of Glycans in the SARS-CoV-2 Spike Protein [J].
Casalino, Lorenzo ;
Gaieb, Zied ;
Goldsmith, Jory A. ;
Hjorth, Christy K. ;
Dommer, Abigail C. ;
Harbison, Aoife M. ;
Fogarty, Carl A. ;
Barros, Emilia P. ;
Taylor, Bryn C. ;
McLellan, Jason S. ;
Fadda, Elisa ;
Amaro, Rommie E. .
ACS CENTRAL SCIENCE, 2020, 6 (10) :1722-1734
[7]   In vitro susceptibility of 10 clinical isolates of SARS coronavirus to selected antiviral compounds [J].
Chen, F ;
Chan, KH ;
Jiang, Y ;
Kao, RYT ;
Lu, HT ;
Fan, KW ;
Cheng, VCC ;
Tsui, WHW ;
Hung, IFN ;
Lee, TSW ;
Guan, Y ;
Peiris, JSM ;
Yuen, KY .
JOURNAL OF CLINICAL VIROLOGY, 2004, 31 (01) :69-75
[8]   Thiopurine analogues inhibit papain-like protease of severe acute respiratory syndrome coronavirus [J].
Chou, Chi-Yuan ;
Chien, Chia-Hui ;
Han, Yu-San ;
Prebanda, Mojca Trstenjak ;
Hsieh, Hsing-Pang ;
Turk, Boris ;
Chang, Gu-Gang ;
Chen, Xin .
BIOCHEMICAL PHARMACOLOGY, 2008, 75 (08) :1601-1609
[9]   Remdesivir, lopinavir, emetine, and homoharringtonine inhibit SARS-CoV-2 replication in vitro [J].
Choy, Ka-Tim ;
Wong, Alvina Yin-Lam ;
Kaewpreedee, Prathanporn ;
Sia, Sin Fun ;
Chen, Dongdong ;
Hui, Kenrie Pui Yan ;
Chu, Daniel Ka Wing ;
Chan, Michael Chi Wai ;
Cheung, Peter Pak-Hang ;
Huang, Xuhui ;
Peiris, Malik ;
Yen, Hui-Ling .
ANTIVIRAL RESEARCH, 2020, 178
[10]  
Clausen TM, 2020, CELL, V183, P1043, DOI [10.1016/j.cell.2020.09.033, 10.1101/2020.07.14.201616]