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Drug design targeting the main protease, the Achilles' heel of coronaviruses : SARS-CoV: A scénario of modern drug design

Identifieur interne : 000567 ( PascalFrancis/Curation ); précédent : 000566; suivant : 000568

Drug design targeting the main protease, the Achilles' heel of coronaviruses : SARS-CoV: A scénario of modern drug design

Auteurs : HAITAO YANG [République populaire de Chine] ; Mark Bartlam ; ZIHE RAO

Source :

RBID : Pascal:07-0053593

Descripteurs français

English descriptors

Abstract

Coronaviruses (CoVs), a genus containing about 26 known species to date, cause highly prevalent diseases and are often severe or fatal in humans and animals. In 2003, a previously unknown coronavirus was identified to be the etiological agent of a global outbreak of a form of life-threatening pneumonia called severe acute respiratory syndrome (SARS). No efficacious therapy is currently available, and vaccines and drugs are under development to prevent SARS-CoV infection in many countries. The CoV main protease (Mpro), which plays a pivotal role in viral gene expression and replication through a highly complex cascade involving the proteolytic processing of replicase polyproteins, is an attractive target for drug design. This review summarizes the recent advances in biological and structural studies, together with development of inhibitors targeting CoV Mpros. It is expected that inhibitors targeting CoV Mpros could be developed into wide-spectrum antiviral drugs against existing and possible future emerging CoV-associated diseases.
pA  
A01 01  1    @0 1381-6128
A03   1    @0 Curr. pharm. des.
A05       @2 12
A06       @2 35
A08 01  1  ENG  @1 Drug design targeting the main protease, the Achilles' heel of coronaviruses : SARS-CoV: A scénario of modern drug design
A11 01  1    @1 HAITAO YANG
A11 02  1    @1 BARTLAM (Mark)
A11 03  1    @1 ZIHE RAO
A14 01      @1 National Laboratory of Biomacromolecules, Institute of Biophysics (IBP), Chinese Academy of Sciences @2 Beijing 100101 @3 CHN
A14 02      @1 Tsinghua-IBP Joint Research Group for Structural Biology, Tsinghua University @2 Beijing 100084 @3 CHN
A20       @1 4573-4590
A21       @1 2006
A23 01      @0 ENG
A43 01      @1 INIST @2 26320 @5 354000145201350040
A44       @0 0000 @1 © 2007 INIST-CNRS. All rights reserved.
A45       @0 131 ref.
A47 01  1    @0 07-0053593
A60       @1 P
A61       @0 A
A64 01  1    @0 Current pharmaceutical design
A66 01      @0 NLD
C01 01    ENG  @0 Coronaviruses (CoVs), a genus containing about 26 known species to date, cause highly prevalent diseases and are often severe or fatal in humans and animals. In 2003, a previously unknown coronavirus was identified to be the etiological agent of a global outbreak of a form of life-threatening pneumonia called severe acute respiratory syndrome (SARS). No efficacious therapy is currently available, and vaccines and drugs are under development to prevent SARS-CoV infection in many countries. The CoV main protease (Mpro), which plays a pivotal role in viral gene expression and replication through a highly complex cascade involving the proteolytic processing of replicase polyproteins, is an attractive target for drug design. This review summarizes the recent advances in biological and structural studies, together with development of inhibitors targeting CoV Mpros. It is expected that inhibitors targeting CoV Mpros could be developed into wide-spectrum antiviral drugs against existing and possible future emerging CoV-associated diseases.
C02 01  X    @0 002B02S05
C03 01  X  FRE  @0 Médicament @5 01
C03 01  X  ENG  @0 Drug @5 01
C03 01  X  SPA  @0 Medicamento @5 01
C03 02  X  FRE  @0 Cible @5 02
C03 02  X  ENG  @0 Target @5 02
C03 02  X  SPA  @0 Blanco @5 02
C03 03  X  FRE  @0 Ciblage @5 03
C03 03  X  ENG  @0 Targeting @5 03
C03 03  X  SPA  @0 Blancado @5 03
C03 04  X  FRE  @0 Peptidases @2 FE @5 04
C03 04  X  ENG  @0 Peptidases @2 FE @5 04
C03 04  X  SPA  @0 Peptidases @2 FE @5 04
C03 05  X  FRE  @0 Coronavirus @2 NW @5 05
C03 05  X  ENG  @0 Coronavirus @2 NW @5 05
C03 05  X  SPA  @0 Coronavirus @2 NW @5 05
C03 06  X  FRE  @0 Article synthèse @5 06
C03 06  X  ENG  @0 Review @5 06
C03 06  X  SPA  @0 Artículo síntesis @5 06
C03 07  X  FRE  @0 Antiviral @5 07
C03 07  X  ENG  @0 Antiviral @5 07
C03 07  X  SPA  @0 Antiviral @5 07
C03 08  X  FRE  @0 Conception @5 08
C03 08  X  ENG  @0 Design @5 08
C03 08  X  SPA  @0 Diseño @5 08
C03 09  X  FRE  @0 Recherche développement @5 09
C03 09  X  ENG  @0 Research and development @5 09
C03 09  X  SPA  @0 Investigación desarrollo @5 09
C03 10  X  FRE  @0 Syndrome respiratoire aigu sévère @2 NM @5 10
C03 10  X  ENG  @0 Severe acute respiratory syndrome @2 NM @5 10
C03 10  X  SPA  @0 Síndrome respiratorio agudo severo @2 NM @5 10
C03 11  X  FRE  @0 Inhibiteur enzyme @5 11
C03 11  X  ENG  @0 Enzyme inhibitor @5 11
C03 11  X  SPA  @0 Inhibidor enzima @5 11
C03 12  X  FRE  @0 Structure moléculaire @5 12
C03 12  X  ENG  @0 Molecular structure @5 12
C03 12  X  SPA  @0 Estructura molecular @5 12
C07 01  X  FRE  @0 Hydrolases @2 FE
C07 01  X  ENG  @0 Hydrolases @2 FE
C07 01  X  SPA  @0 Hydrolases @2 FE
C07 02  X  FRE  @0 Enzyme @2 FE
C07 02  X  ENG  @0 Enzyme @2 FE
C07 02  X  SPA  @0 Enzima @2 FE
C07 03  X  FRE  @0 Coronaviridae @2 NW
C07 03  X  ENG  @0 Coronaviridae @2 NW
C07 03  X  SPA  @0 Coronaviridae @2 NW
C07 04  X  FRE  @0 Nidovirales @2 NW
C07 04  X  ENG  @0 Nidovirales @2 NW
C07 04  X  SPA  @0 Nidovirales @2 NW
C07 05  X  FRE  @0 Virus @2 NW
C07 05  X  ENG  @0 Virus @2 NW
C07 05  X  SPA  @0 Virus @2 NW
C07 06  X  FRE  @0 Virose
C07 06  X  ENG  @0 Viral disease
C07 06  X  SPA  @0 Virosis
C07 07  X  FRE  @0 Infection
C07 07  X  ENG  @0 Infection
C07 07  X  SPA  @0 Infección
C07 08  X  FRE  @0 Appareil respiratoire pathologie @5 37
C07 08  X  ENG  @0 Respiratory disease @5 37
C07 08  X  SPA  @0 Aparato respiratorio patología @5 37
C07 09  X  FRE  @0 Poumon pathologie @5 38
C07 09  X  ENG  @0 Lung disease @5 38
C07 09  X  SPA  @0 Pulmón patología @5 38
N21       @1 036

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Pascal:07-0053593

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<term>Molecular structure</term>
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<term>Review</term>
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<div type="abstract" xml:lang="en">Coronaviruses (CoVs), a genus containing about 26 known species to date, cause highly prevalent diseases and are often severe or fatal in humans and animals. In 2003, a previously unknown coronavirus was identified to be the etiological agent of a global outbreak of a form of life-threatening pneumonia called severe acute respiratory syndrome (SARS). No efficacious therapy is currently available, and vaccines and drugs are under development to prevent SARS-CoV infection in many countries. The CoV main protease (M
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<sup>pro</sup>
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<sup>pro</sup>
s could be developed into wide-spectrum antiviral drugs against existing and possible future emerging CoV-associated diseases.</div>
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<s0>Coronaviruses (CoVs), a genus containing about 26 known species to date, cause highly prevalent diseases and are often severe or fatal in humans and animals. In 2003, a previously unknown coronavirus was identified to be the etiological agent of a global outbreak of a form of life-threatening pneumonia called severe acute respiratory syndrome (SARS). No efficacious therapy is currently available, and vaccines and drugs are under development to prevent SARS-CoV infection in many countries. The CoV main protease (M
<sup>pro</sup>
), which plays a pivotal role in viral gene expression and replication through a highly complex cascade involving the proteolytic processing of replicase polyproteins, is an attractive target for drug design. This review summarizes the recent advances in biological and structural studies, together with development of inhibitors targeting CoV M
<sup>pro</sup>
s. It is expected that inhibitors targeting CoV M
<sup>pro</sup>
s could be developed into wide-spectrum antiviral drugs against existing and possible future emerging CoV-associated diseases.</s0>
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<s2>FE</s2>
<s5>04</s5>
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<s5>04</s5>
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<s2>NW</s2>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Coronavirus</s0>
<s2>NW</s2>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Coronavirus</s0>
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<s5>07</s5>
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<s5>07</s5>
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<s0>Antiviral</s0>
<s5>07</s5>
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<fC03 i1="08" i2="X" l="FRE">
<s0>Conception</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG">
<s0>Design</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA">
<s0>Diseño</s0>
<s5>08</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE">
<s0>Recherche développement</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG">
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<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA">
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<s5>09</s5>
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<s5>10</s5>
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<fC03 i1="10" i2="X" l="SPA">
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<s5>12</s5>
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<s2>FE</s2>
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<fC07 i1="02" i2="X" l="SPA">
<s0>Enzima</s0>
<s2>FE</s2>
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<fC07 i1="03" i2="X" l="FRE">
<s0>Coronaviridae</s0>
<s2>NW</s2>
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<fC07 i1="03" i2="X" l="ENG">
<s0>Coronaviridae</s0>
<s2>NW</s2>
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<s2>NW</s2>
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<fC07 i1="04" i2="X" l="SPA">
<s0>Nidovirales</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="05" i2="X" l="FRE">
<s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="05" i2="X" l="ENG">
<s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="05" i2="X" l="SPA">
<s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="06" i2="X" l="FRE">
<s0>Virose</s0>
</fC07>
<fC07 i1="06" i2="X" l="ENG">
<s0>Viral disease</s0>
</fC07>
<fC07 i1="06" i2="X" l="SPA">
<s0>Virosis</s0>
</fC07>
<fC07 i1="07" i2="X" l="FRE">
<s0>Infection</s0>
</fC07>
<fC07 i1="07" i2="X" l="ENG">
<s0>Infection</s0>
</fC07>
<fC07 i1="07" i2="X" l="SPA">
<s0>Infección</s0>
</fC07>
<fC07 i1="08" i2="X" l="FRE">
<s0>Appareil respiratoire pathologie</s0>
<s5>37</s5>
</fC07>
<fC07 i1="08" i2="X" l="ENG">
<s0>Respiratory disease</s0>
<s5>37</s5>
</fC07>
<fC07 i1="08" i2="X" l="SPA">
<s0>Aparato respiratorio patología</s0>
<s5>37</s5>
</fC07>
<fC07 i1="09" i2="X" l="FRE">
<s0>Poumon pathologie</s0>
<s5>38</s5>
</fC07>
<fC07 i1="09" i2="X" l="ENG">
<s0>Lung disease</s0>
<s5>38</s5>
</fC07>
<fC07 i1="09" i2="X" l="SPA">
<s0>Pulmón patología</s0>
<s5>38</s5>
</fC07>
<fN21>
<s1>036</s1>
</fN21>
</pA>
</standard>
</inist>
</record>

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{{Explor lien
   |wiki=    Sante
   |area=    SrasV1
   |flux=    PascalFrancis
   |étape=   Curation
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   |texte=   Drug design targeting the main protease, the Achilles' heel of coronaviruses : SARS-CoV: A scénario of modern drug design
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