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Oridonin Inhibits SARS‐CoV‐2 by Targeting Its 3C‐Like Protease
Oridonin Inhibits SARS‐CoV‐2 Oridonin, a natural product extracted from Rabdosia rubescens, possesses a wide range of pharmacological properties, including anti‐inflammatory, anti‐cancer, anti‐microbial, neuroprotection, immunoregulation, etc. In article number 2100124, Baisen Zhong, Litao Sun, and...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9347789/ https://www.ncbi.nlm.nih.gov/pubmed/35942318 http://dx.doi.org/10.1002/smsc.202270012 |
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author | Zhong, Baisen Peng, Weiyu Du, Shan Chen, Bingyi Feng, Yajuan Hu, Xinfeng Lai, Qi Liu, Shujie Zhou, Zhong-Wei Fang, Pengfei Wu, Yan Gao, Feng Zhou, Huihao Sun, Litao |
author_facet | Zhong, Baisen Peng, Weiyu Du, Shan Chen, Bingyi Feng, Yajuan Hu, Xinfeng Lai, Qi Liu, Shujie Zhou, Zhong-Wei Fang, Pengfei Wu, Yan Gao, Feng Zhou, Huihao Sun, Litao |
author_sort | Zhong, Baisen |
collection | PubMed |
description | Oridonin Inhibits SARS‐CoV‐2 Oridonin, a natural product extracted from Rabdosia rubescens, possesses a wide range of pharmacological properties, including anti‐inflammatory, anti‐cancer, anti‐microbial, neuroprotection, immunoregulation, etc. In article number 2100124, Baisen Zhong, Litao Sun, and co‐workers demonstrate that Oridonin targets the SARS‐CoV‐2 3CL protease by covalently binding to cysteine145 in its active pocket to exert an anti‐SARS‐CoV‐2 effect, which provides a novel candidate for the treatment of COVID‐19. [Image: see text] |
format | Online Article Text |
id | pubmed-9347789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93477892022-08-04 Oridonin Inhibits SARS‐CoV‐2 by Targeting Its 3C‐Like Protease Zhong, Baisen Peng, Weiyu Du, Shan Chen, Bingyi Feng, Yajuan Hu, Xinfeng Lai, Qi Liu, Shujie Zhou, Zhong-Wei Fang, Pengfei Wu, Yan Gao, Feng Zhou, Huihao Sun, Litao Small Sci Cover Picture Oridonin Inhibits SARS‐CoV‐2 Oridonin, a natural product extracted from Rabdosia rubescens, possesses a wide range of pharmacological properties, including anti‐inflammatory, anti‐cancer, anti‐microbial, neuroprotection, immunoregulation, etc. In article number 2100124, Baisen Zhong, Litao Sun, and co‐workers demonstrate that Oridonin targets the SARS‐CoV‐2 3CL protease by covalently binding to cysteine145 in its active pocket to exert an anti‐SARS‐CoV‐2 effect, which provides a novel candidate for the treatment of COVID‐19. [Image: see text] John Wiley and Sons Inc. 2022-06-12 2022-06 /pmc/articles/PMC9347789/ /pubmed/35942318 http://dx.doi.org/10.1002/smsc.202270012 Text en © 2022 Wiley‐VCH GmbH https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Cover Picture Zhong, Baisen Peng, Weiyu Du, Shan Chen, Bingyi Feng, Yajuan Hu, Xinfeng Lai, Qi Liu, Shujie Zhou, Zhong-Wei Fang, Pengfei Wu, Yan Gao, Feng Zhou, Huihao Sun, Litao Oridonin Inhibits SARS‐CoV‐2 by Targeting Its 3C‐Like Protease |
title | Oridonin Inhibits SARS‐CoV‐2 by Targeting Its 3C‐Like Protease |
title_full | Oridonin Inhibits SARS‐CoV‐2 by Targeting Its 3C‐Like Protease |
title_fullStr | Oridonin Inhibits SARS‐CoV‐2 by Targeting Its 3C‐Like Protease |
title_full_unstemmed | Oridonin Inhibits SARS‐CoV‐2 by Targeting Its 3C‐Like Protease |
title_short | Oridonin Inhibits SARS‐CoV‐2 by Targeting Its 3C‐Like Protease |
title_sort | oridonin inhibits sars‐cov‐2 by targeting its 3c‐like protease |
topic | Cover Picture |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9347789/ https://www.ncbi.nlm.nih.gov/pubmed/35942318 http://dx.doi.org/10.1002/smsc.202270012 |
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