Antiviral drug discovery against SARS-CoV
Identifieur interne : 000504 ( PascalFrancis/Checkpoint ); précédent : 000503; suivant : 000505Antiviral drug discovery against SARS-CoV
Auteurs : Yu-Shan Wu [Taïwan] ; Wen-Hsing Lin [Taïwan] ; John T.-A. Hsu [Taïwan] ; Hsing-Pang Flsieh [Taïwan]Source :
- Current medicinal chemistry [ 0929-8673 ] ; 2006.
Descripteurs français
- Pascal (Inist)
- Antiviral, Recherche développement, Médicament, Virus syndrome respiratoire aigu sévère, Article synthèse, Criblage haut débit, Ciblage, Synthèse chimique, Peptide, Analogue, Composé non peptide, Inhibiteur protease, siRNA, Relation structure activité, Inhibiteur enzyme, Peptidases, RNA antisens, Criblage virtuel.
- Wicri :
- topic : Médicament.
English descriptors
- KwdEn :
- Analog, Antisense RNA, Antiviral, Chemical synthesis, Drug, Enzyme inhibitor, High throughput screening, Non peptide compound, Peptidases, Peptides, Protease inhibitor, Research and development, Review, Severe acute respiratory syndrome virus, Small Interference RNA, Structure activity relation, Targeting, Virtual screening.
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 Mpro; 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.
Affiliations:
Links toward previous steps (curation, corpus...)
Links to Exploration step
Pascal:06-0496072Le 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<sup>pro</sup>
; 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>
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<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="FRE"><s0>Coronaviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Coronaviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Coronaviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Nidovirales</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Nidovirales</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Nidovirales</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Hydrolases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Hydrolases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Hydrolases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Enzyme</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Enzyme</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Enzima</s0>
<s2>FE</s2>
</fC07>
<fN21><s1>324</s1>
</fN21>
</pA>
</standard>
</inist>
<affiliations><list><country><li>Taïwan</li>
</country>
</list>
<tree><country name="Taïwan"><noRegion><name sortKey="Wu, Yu Shan" sort="Wu, Yu Shan" uniqKey="Wu Y" first="Yu-Shan" last="Wu">Yu-Shan Wu</name>
</noRegion>
<name sortKey="Flsieh, Hsing Pang" sort="Flsieh, Hsing Pang" uniqKey="Flsieh H" first="Hsing-Pang" last="Flsieh">Hsing-Pang Flsieh</name>
<name sortKey="Hsu, John T A" sort="Hsu, John T A" uniqKey="Hsu J" first="John T.-A." last="Hsu">John T.-A. Hsu</name>
<name sortKey="Hsu, John T A" sort="Hsu, John T A" uniqKey="Hsu J" first="John T.-A." last="Hsu">John T.-A. Hsu</name>
<name sortKey="Lin, Wen Hsing" sort="Lin, Wen Hsing" uniqKey="Lin W" first="Wen-Hsing" last="Lin">Wen-Hsing Lin</name>
</country>
</tree>
</affiliations>
</record>
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