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Synthesis and activity of an octapeptide inhibitor designed for SARS coronavirus main proteinase.

Identifieur interne : 003C80 ( Main/Exploration ); précédent : 003C79; suivant : 003C81

Synthesis and activity of an octapeptide inhibitor designed for SARS coronavirus main proteinase.

Auteurs : Yi-Ru Gan [République populaire de Chine] ; He Huang ; Yong-Dong Huang ; Chun-Ming Rao ; Yang Zhao ; Jin-Sheng Liu ; Lei Wu ; Dong-Qing Wei

Source :

RBID : pubmed:16242214

Descripteurs français

English descriptors

Abstract

The outbreak of SARS, a life-threatening disease, has spread over many countries around the world. So far there is no effective drug for the treatment of SARS. Stimulated by the binding mechanism of SARS-CoV Mpro with the octapeptide AVLQSGFR reported recently as well as the "Chou's distorted key" theory, we synthesized the octapeptide AVLQSGFR for conducting various biochemical experiments to investigate the antiviral potential of the octapeptide against SARS coronavirus (BJ-01). The results demonstrate that, compared with other compounds reported so far, AVLQSGFR is the most active in inhibiting replication of the SARS coronavirus, and that no detectable toxicity is observed on Vero cells under the condition of experimental concentration.

DOI: 10.1016/j.peptides.2005.09.006
PubMed: 16242214


Affiliations:


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Le document en format XML

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<name sortKey="Zhao, Yang" sort="Zhao, Yang" uniqKey="Zhao Y" first="Yang" last="Zhao">Yang Zhao</name>
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<div type="abstract" xml:lang="en">The outbreak of SARS, a life-threatening disease, has spread over many countries around the world. So far there is no effective drug for the treatment of SARS. Stimulated by the binding mechanism of SARS-CoV Mpro with the octapeptide AVLQSGFR reported recently as well as the "Chou's distorted key" theory, we synthesized the octapeptide AVLQSGFR for conducting various biochemical experiments to investigate the antiviral potential of the octapeptide against SARS coronavirus (BJ-01). The results demonstrate that, compared with other compounds reported so far, AVLQSGFR is the most active in inhibiting replication of the SARS coronavirus, and that no detectable toxicity is observed on Vero cells under the condition of experimental concentration.</div>
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