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Individual and common inhibitors of coronavirus and picornavirus main proteases

Picornaviruses (PV) and coronaviruses (CoV) are positive‐stranded RNA viruses which infect millions of people worldwide each year, resulting in a wide range of clinical outcomes. As reported in this study, using high throughput screening against ∼6800 small molecules, we have identified several nove...

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Autores principales: Kuo, Chih-Jung, Liu, Hun-Ge, Lo, Yueh-Kuei, Seong, Churl-Min, Lee, Kee-In, Jung, Young-Sik, Liang, Po-Huang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094298/
https://www.ncbi.nlm.nih.gov/pubmed/19166843
http://dx.doi.org/10.1016/j.febslet.2008.12.059
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author Kuo, Chih-Jung
Liu, Hun-Ge
Lo, Yueh-Kuei
Seong, Churl-Min
Lee, Kee-In
Jung, Young-Sik
Liang, Po-Huang
author_facet Kuo, Chih-Jung
Liu, Hun-Ge
Lo, Yueh-Kuei
Seong, Churl-Min
Lee, Kee-In
Jung, Young-Sik
Liang, Po-Huang
author_sort Kuo, Chih-Jung
collection PubMed
description Picornaviruses (PV) and coronaviruses (CoV) are positive‐stranded RNA viruses which infect millions of people worldwide each year, resulting in a wide range of clinical outcomes. As reported in this study, using high throughput screening against ∼6800 small molecules, we have identified several novel inhibitors of SARS‐CoV 3CL(pro) with IC(50) of low μM. Interestingly, one of them equally inhibited both 3C(pro) and 3CL(pro) from PV and CoV, respectively. Using computer modeling, the structural features of these compounds as individual and common protease inhibitors were elucidated to enhance our knowledge for developing anti‐viral agents against PV and CoV.
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spelling pubmed-70942982020-03-25 Individual and common inhibitors of coronavirus and picornavirus main proteases Kuo, Chih-Jung Liu, Hun-Ge Lo, Yueh-Kuei Seong, Churl-Min Lee, Kee-In Jung, Young-Sik Liang, Po-Huang FEBS Lett Short Communications Picornaviruses (PV) and coronaviruses (CoV) are positive‐stranded RNA viruses which infect millions of people worldwide each year, resulting in a wide range of clinical outcomes. As reported in this study, using high throughput screening against ∼6800 small molecules, we have identified several novel inhibitors of SARS‐CoV 3CL(pro) with IC(50) of low μM. Interestingly, one of them equally inhibited both 3C(pro) and 3CL(pro) from PV and CoV, respectively. Using computer modeling, the structural features of these compounds as individual and common protease inhibitors were elucidated to enhance our knowledge for developing anti‐viral agents against PV and CoV. John Wiley and Sons Inc. 2009-02-04 2009-01-21 /pmc/articles/PMC7094298/ /pubmed/19166843 http://dx.doi.org/10.1016/j.febslet.2008.12.059 Text en FEBS Letters 583 (2009) 1873-3468 © 2015 Federation of European Biochemical Societies This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.
spellingShingle Short Communications
Kuo, Chih-Jung
Liu, Hun-Ge
Lo, Yueh-Kuei
Seong, Churl-Min
Lee, Kee-In
Jung, Young-Sik
Liang, Po-Huang
Individual and common inhibitors of coronavirus and picornavirus main proteases
title Individual and common inhibitors of coronavirus and picornavirus main proteases
title_full Individual and common inhibitors of coronavirus and picornavirus main proteases
title_fullStr Individual and common inhibitors of coronavirus and picornavirus main proteases
title_full_unstemmed Individual and common inhibitors of coronavirus and picornavirus main proteases
title_short Individual and common inhibitors of coronavirus and picornavirus main proteases
title_sort individual and common inhibitors of coronavirus and picornavirus main proteases
topic Short Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094298/
https://www.ncbi.nlm.nih.gov/pubmed/19166843
http://dx.doi.org/10.1016/j.febslet.2008.12.059
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