Antiviral drug discovery against SARS-CoV.
Identifieur interne : 001575 ( Ncbi/Checkpoint ); précédent : 001574; suivant : 001576Antiviral drug discovery against SARS-CoV.
Auteurs : Yu-Shan Wu [Taïwan] ; Wen-Hsing Lin ; John T-A Hsu ; Hsing-Pang HsiehSource :
- Current medicinal chemistry [ 0929-8673 ] ; 2006.
Descripteurs français
- KwdFr :
- Animaux, Antiviraux (pharmacologie), Cysteine endopeptidases, Humains, Inhibiteurs de protéases (pharmacologie), Méthode des plages virales, Peptides (analyse), Protéines virales (antagonistes et inhibiteurs), RNA replicase (antagonistes et inhibiteurs), Tests de sensibilité microbienne (), Virus du SRAS ().
- MESH :
- analyse : Peptides.
- antagonistes et inhibiteurs : Protéines virales, RNA replicase.
- pharmacologie : Antiviraux, Inhibiteurs de protéases.
- Animaux, Cysteine endopeptidases, Humains, Méthode des plages virales, Tests de sensibilité microbienne, Virus du SRAS.
English descriptors
- KwdEn :
- Animals, Antiviral Agents (pharmacology), Cysteine Endopeptidases, Humans, Microbial Sensitivity Tests (methods), Peptides (analysis), Protease Inhibitors (pharmacology), RNA Replicase (antagonists & inhibitors), SARS Virus (drug effects), Viral Plaque Assay, Viral Proteins (antagonists & inhibitors).
- MESH :
- chemical , analysis : Peptides.
- chemical , antagonists & inhibitors : RNA Replicase, Viral Proteins.
- chemical , pharmacology : Antiviral Agents, Protease Inhibitors.
- drug effects : SARS Virus.
- methods : Microbial Sensitivity Tests.
- Animals, Cysteine Endopeptidases, Humans, Viral Plaque Assay.
Abstract
Severe Acute Respiratory Syndrome (SARS) is a life-threatening infectious disease caused by SARS-CoV. In the 2003 outbreak, it infected more than 8,000 people worldwide and claimed the lives of more than 900 victims. The high mortality rate resulted, at least in part, from the absence of definitive treatment protocols or therapeutic agents. Although the virus spreading has been contained, due preparedness and planning, including the successful development of antiviral drugs against SARS-CoV, is necessary for possible reappearance of SARS. In this review, we have discussed currently available strategies for antiviral drug discovery and how these technologies have been utilized to identify potential antiviral agents for the inhibition of SARS-CoV replication. Moreover, progress in the drug development based on different molecular targets is also summarized, including 1) Compounds that block the S protein-ACE2-mediated viral entry; 2) Compounds targeting SARS-CoV M(pro); 3) Compounds targeting papain-like protease 2 (PLP2); 4) Compounds targeting SARS-CoV RdRp; 5) Compounds targeting SARS-CoV helicase; 6) Active compounds with unspecified targets; and 7) Research on siRNA. This review aims to provide a comprehensive account of drug discovery on SARS. The experiences with the SARS outbreak and drug discovery would certainly be an important lesson for the drug development for any new viral outbreaks that may emerge in the future.
DOI: 10.2174/092986706777584988
PubMed: 16842194
Affiliations:
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pubmed:16842194Le document en format XML
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<front><div type="abstract" xml:lang="en">Severe Acute Respiratory Syndrome (SARS) is a life-threatening infectious disease caused by SARS-CoV. In the 2003 outbreak, it infected more than 8,000 people worldwide and claimed the lives of more than 900 victims. The high mortality rate resulted, at least in part, from the absence of definitive treatment protocols or therapeutic agents. Although the virus spreading has been contained, due preparedness and planning, including the successful development of antiviral drugs against SARS-CoV, is necessary for possible reappearance of SARS. In this review, we have discussed currently available strategies for antiviral drug discovery and how these technologies have been utilized to identify potential antiviral agents for the inhibition of SARS-CoV replication. Moreover, progress in the drug development based on different molecular targets is also summarized, including 1) Compounds that block the S protein-ACE2-mediated viral entry; 2) Compounds targeting SARS-CoV M(pro); 3) Compounds targeting papain-like protease 2 (PLP2); 4) Compounds targeting SARS-CoV RdRp; 5) Compounds targeting SARS-CoV helicase; 6) Active compounds with unspecified targets; and 7) Research on siRNA. This review aims to provide a comprehensive account of drug discovery on SARS. The experiences with the SARS outbreak and drug discovery would certainly be an important lesson for the drug development for any new viral outbreaks that may emerge in the future.</div>
</front>
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