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An Overview of Severe Acute Respiratory Syndrome–Coronavirus (SARS-CoV) 3CL Protease Inhibitors: Peptidomimetics and Small Molecule Chemotherapy
[Image: see text] Severe acute respiratory syndrome (SARS) is caused by a newly emerged coronavirus that infected more than 8000 individuals and resulted in more than 800 (10–15%) fatalities in 2003. The causative agent of SARS has been identified as a novel human coronavirus (SARS-CoV), and its vir...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7075650/ https://www.ncbi.nlm.nih.gov/pubmed/26878082 http://dx.doi.org/10.1021/acs.jmedchem.5b01461 |
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author | Pillaiyar, Thanigaimalai Manickam, Manoj Namasivayam, Vigneshwaran Hayashi, Yoshio Jung, Sang-Hun |
author_facet | Pillaiyar, Thanigaimalai Manickam, Manoj Namasivayam, Vigneshwaran Hayashi, Yoshio Jung, Sang-Hun |
author_sort | Pillaiyar, Thanigaimalai |
collection | PubMed |
description | [Image: see text] Severe acute respiratory syndrome (SARS) is caused by a newly emerged coronavirus that infected more than 8000 individuals and resulted in more than 800 (10–15%) fatalities in 2003. The causative agent of SARS has been identified as a novel human coronavirus (SARS-CoV), and its viral protease, SARS-CoV 3CL(pro), has been shown to be essential for replication and has hence been recognized as a potent drug target for SARS infection. Currently, there is no effective treatment for this epidemic despite the intensive research that has been undertaken since 2003 (over 3500 publications). This perspective focuses on the status of various efficacious anti-SARS-CoV 3CL(pro) chemotherapies discovered during the last 12 years (2003–2015) from all sources, including laboratory synthetic methods, natural products, and virtual screening. We describe here mainly peptidomimetic and small molecule inhibitors of SARS-CoV 3CL(pro). Attempts have been made to provide a complete description of the structural features and binding modes of these inhibitors under many conditions. |
format | Online Article Text |
id | pubmed-7075650 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-70756502020-03-17 An Overview of Severe Acute Respiratory Syndrome–Coronavirus (SARS-CoV) 3CL Protease Inhibitors: Peptidomimetics and Small Molecule Chemotherapy Pillaiyar, Thanigaimalai Manickam, Manoj Namasivayam, Vigneshwaran Hayashi, Yoshio Jung, Sang-Hun J Med Chem [Image: see text] Severe acute respiratory syndrome (SARS) is caused by a newly emerged coronavirus that infected more than 8000 individuals and resulted in more than 800 (10–15%) fatalities in 2003. The causative agent of SARS has been identified as a novel human coronavirus (SARS-CoV), and its viral protease, SARS-CoV 3CL(pro), has been shown to be essential for replication and has hence been recognized as a potent drug target for SARS infection. Currently, there is no effective treatment for this epidemic despite the intensive research that has been undertaken since 2003 (over 3500 publications). This perspective focuses on the status of various efficacious anti-SARS-CoV 3CL(pro) chemotherapies discovered during the last 12 years (2003–2015) from all sources, including laboratory synthetic methods, natural products, and virtual screening. We describe here mainly peptidomimetic and small molecule inhibitors of SARS-CoV 3CL(pro). Attempts have been made to provide a complete description of the structural features and binding modes of these inhibitors under many conditions. American Chemical Society 2016-02-15 2016-07-28 /pmc/articles/PMC7075650/ /pubmed/26878082 http://dx.doi.org/10.1021/acs.jmedchem.5b01461 Text en Copyright © 2016 American Chemical Society This article is made available for a limited time sponsored by ACS under the ACS Free to Read License (http://pubs.acs.org/page/policy/freetoread/index.html) , which permits copying and redistribution of the article for non-commercial scholarly purposes. |
spellingShingle | Pillaiyar, Thanigaimalai Manickam, Manoj Namasivayam, Vigneshwaran Hayashi, Yoshio Jung, Sang-Hun An Overview of Severe Acute Respiratory Syndrome–Coronavirus (SARS-CoV) 3CL Protease Inhibitors: Peptidomimetics and Small Molecule Chemotherapy |
title | An Overview of
Severe Acute Respiratory Syndrome–Coronavirus
(SARS-CoV) 3CL Protease Inhibitors: Peptidomimetics and Small Molecule
Chemotherapy |
title_full | An Overview of
Severe Acute Respiratory Syndrome–Coronavirus
(SARS-CoV) 3CL Protease Inhibitors: Peptidomimetics and Small Molecule
Chemotherapy |
title_fullStr | An Overview of
Severe Acute Respiratory Syndrome–Coronavirus
(SARS-CoV) 3CL Protease Inhibitors: Peptidomimetics and Small Molecule
Chemotherapy |
title_full_unstemmed | An Overview of
Severe Acute Respiratory Syndrome–Coronavirus
(SARS-CoV) 3CL Protease Inhibitors: Peptidomimetics and Small Molecule
Chemotherapy |
title_short | An Overview of
Severe Acute Respiratory Syndrome–Coronavirus
(SARS-CoV) 3CL Protease Inhibitors: Peptidomimetics and Small Molecule
Chemotherapy |
title_sort | overview of
severe acute respiratory syndrome–coronavirus
(sars-cov) 3cl protease inhibitors: peptidomimetics and small molecule
chemotherapy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7075650/ https://www.ncbi.nlm.nih.gov/pubmed/26878082 http://dx.doi.org/10.1021/acs.jmedchem.5b01461 |
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