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Research progress on repositioning drugs and specific therapeutic drugs for SARS-CoV-2

SARS-CoV-2 has been widely spread around the world and COVID-19 was declared a global pandemic by the World Health Organization. Limited clinically effective antiviral drugs are available now. The development of anti-SARS-CoV-2 drugs has become an urgent work worldwide. At present, potential therape...

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Detalles Bibliográficos
Autores principales: Fan, Shiyong, Xiao, Dian, Wang, Yanming, Liu, Lianqi, Zhou, Xinbo, Zhong, Wu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Newlands Press Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7341957/
https://www.ncbi.nlm.nih.gov/pubmed/32638628
http://dx.doi.org/10.4155/fmc-2020-0158
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author Fan, Shiyong
Xiao, Dian
Wang, Yanming
Liu, Lianqi
Zhou, Xinbo
Zhong, Wu
author_facet Fan, Shiyong
Xiao, Dian
Wang, Yanming
Liu, Lianqi
Zhou, Xinbo
Zhong, Wu
author_sort Fan, Shiyong
collection PubMed
description SARS-CoV-2 has been widely spread around the world and COVID-19 was declared a global pandemic by the World Health Organization. Limited clinically effective antiviral drugs are available now. The development of anti-SARS-CoV-2 drugs has become an urgent work worldwide. At present, potential therapeutic targets and drugs for SARS-CoV-2 are continuously reported, and many repositioning drugs are undergoing extensive clinical research, including remdesivir and chloroquine. On the other hand, structures of many important viral target proteins and host target proteins, including that of RdRp and Mpro were constantly reported, which greatly promoted structure-based drug design. This paper summarizes the current research progress and challenges in the development of anti-SARS-CoV-2 drugs, and proposes novel short-term and long-term drug research strategies.
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spelling pubmed-73419572020-07-08 Research progress on repositioning drugs and specific therapeutic drugs for SARS-CoV-2 Fan, Shiyong Xiao, Dian Wang, Yanming Liu, Lianqi Zhou, Xinbo Zhong, Wu Future Med Chem Review SARS-CoV-2 has been widely spread around the world and COVID-19 was declared a global pandemic by the World Health Organization. Limited clinically effective antiviral drugs are available now. The development of anti-SARS-CoV-2 drugs has become an urgent work worldwide. At present, potential therapeutic targets and drugs for SARS-CoV-2 are continuously reported, and many repositioning drugs are undergoing extensive clinical research, including remdesivir and chloroquine. On the other hand, structures of many important viral target proteins and host target proteins, including that of RdRp and Mpro were constantly reported, which greatly promoted structure-based drug design. This paper summarizes the current research progress and challenges in the development of anti-SARS-CoV-2 drugs, and proposes novel short-term and long-term drug research strategies. Newlands Press Ltd 2020-07-08 2020-06 /pmc/articles/PMC7341957/ /pubmed/32638628 http://dx.doi.org/10.4155/fmc-2020-0158 Text en © 2020 Newlands Press This work is licensed under the Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/)
spellingShingle Review
Fan, Shiyong
Xiao, Dian
Wang, Yanming
Liu, Lianqi
Zhou, Xinbo
Zhong, Wu
Research progress on repositioning drugs and specific therapeutic drugs for SARS-CoV-2
title Research progress on repositioning drugs and specific therapeutic drugs for SARS-CoV-2
title_full Research progress on repositioning drugs and specific therapeutic drugs for SARS-CoV-2
title_fullStr Research progress on repositioning drugs and specific therapeutic drugs for SARS-CoV-2
title_full_unstemmed Research progress on repositioning drugs and specific therapeutic drugs for SARS-CoV-2
title_short Research progress on repositioning drugs and specific therapeutic drugs for SARS-CoV-2
title_sort research progress on repositioning drugs and specific therapeutic drugs for sars-cov-2
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7341957/
https://www.ncbi.nlm.nih.gov/pubmed/32638628
http://dx.doi.org/10.4155/fmc-2020-0158
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