An Overview of Severe Acute Respiratory Syndrome–Coronavirus (SARS-CoV) 3CL Protease Inhibitors: Peptidomimetics and Small Molecule Chemotherapy
Identifieur interne : 001083 ( Main/Exploration ); précédent : 001082; suivant : 001084An Overview of Severe Acute Respiratory Syndrome–Coronavirus (SARS-CoV) 3CL Protease Inhibitors: Peptidomimetics and Small Molecule Chemotherapy
Auteurs : Thanigaimalai Pillaiyar [Allemagne] ; Manoj Manickam [Corée du Sud] ; Vigneshwaran Namasivayam [Allemagne] ; Yoshio Hayashi [Japon] ; Sang-Hun Jung [Corée du Sud]Source :
- Journal of Medicinal Chemistry [ 0022-2623 ] ; 2016.
Abstract
Severe acute respiratory syndrome (SARS) is caused by a newly emerged coronavirus that infected more than 8000 individuals and resulted in more than 800 (10–15%) fatalities in 2003. The causative agent of SARS has been identified as a novel human coronavirus (SARS-CoV), and its viral protease, SARS-CoV 3CLpro, has been shown to be essential for replication and has hence been recognized as a potent drug target for SARS infection. Currently, there is no effective treatment for this epidemic despite the intensive research that has been undertaken since 2003 (over 3500 publications). This perspective focuses on the status of various efficacious anti-SARS-CoV 3CLpro chemotherapies discovered during the last 12 years (2003–2015) from all sources, including laboratory synthetic methods, natural products, and virtual screening. We describe here mainly peptidomimetic and small molecule inhibitors of SARS-CoV 3CLpro. Attempts have been made to provide a complete description of the structural features and binding modes of these inhibitors under many conditions.
Url:
DOI: 10.1021/acs.jmedchem.5b01461
PubMed: 26878082
PubMed Central: 7075650
Affiliations:
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Severe Acute Respiratory Syndrome–Coronavirus
(SARS-CoV) 3CL Protease Inhibitors: Peptidomimetics and Small Molecule
Chemotherapy</title><author><name sortKey="Pillaiyar, Thanigaimalai" sort="Pillaiyar, Thanigaimalai" uniqKey="Pillaiyar T" first="Thanigaimalai" last="Pillaiyar">Thanigaimalai Pillaiyar</name><affiliation wicri:level="1"><nlm:aff id="aff1">Pharmaceutical Institute, Pharmaceutical Chemistry I,<institution>University of Bonn</institution>, An der Immenburg 4, D-53121 Bonn,<country>Germany</country></nlm:aff><country xml:lang="fr">Allemagne</country><wicri:regionArea># see nlm:aff country strict</wicri:regionArea></affiliation></author><author><name sortKey="Manickam, Manoj" sort="Manickam, Manoj" uniqKey="Manickam M" first="Manoj" last="Manickam">Manoj Manickam</name><affiliation wicri:level="1"><nlm:aff id="aff3">College of Pharmacy and Institute of Drug Research and Development,<institution>Chungnam National University</institution>, Daejeon 34134,<country>South Korea</country></nlm:aff><country xml:lang="fr">Corée du Sud</country><wicri:regionArea># see nlm:aff country strict</wicri:regionArea></affiliation></author><author><name sortKey="Namasivayam, Vigneshwaran" sort="Namasivayam, Vigneshwaran" uniqKey="Namasivayam V" first="Vigneshwaran" last="Namasivayam">Vigneshwaran Namasivayam</name><affiliation wicri:level="1"><nlm:aff id="aff1">Pharmaceutical Institute, Pharmaceutical Chemistry I,<institution>University of Bonn</institution>, An der Immenburg 4, D-53121 Bonn,<country>Germany</country></nlm:aff><country xml:lang="fr">Allemagne</country><wicri:regionArea># see nlm:aff country strict</wicri:regionArea></affiliation></author><author><name sortKey="Hayashi, Yoshio" sort="Hayashi, Yoshio" uniqKey="Hayashi Y" first="Yoshio" last="Hayashi">Yoshio Hayashi</name><affiliation wicri:level="1"><nlm:aff id="aff2">Department of Medicinal Chemistry,<institution>Tokyo University of Pharmacy and Life Sciences</institution>, Tokyo 192-0392,<country>Japan</country></nlm:aff><country xml:lang="fr">Japon</country><wicri:regionArea># see nlm:aff country strict</wicri:regionArea></affiliation></author><author><name sortKey="Jung, Sang Hun" sort="Jung, Sang Hun" uniqKey="Jung S" first="Sang-Hun" last="Jung">Sang-Hun Jung</name><affiliation wicri:level="1"><nlm:aff id="aff3">College of Pharmacy and Institute of Drug Research and Development,<institution>Chungnam National University</institution>, Daejeon 34134,<country>South Korea</country></nlm:aff><country xml:lang="fr">Corée du Sud</country><wicri:regionArea># see nlm:aff country strict</wicri:regionArea></affiliation></author></analytic><series><title level="j">Journal of Medicinal Chemistry</title><idno type="ISSN">0022-2623</idno><idno type="eISSN">1520-4804</idno><imprint><date when="2016">2016</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p content-type="toc-graphic"><graphic xlink:href="jm5b01461_0045" id="ab-tgr1"></graphic></p><p>Severe
acute respiratory syndrome (SARS) is caused by a newly emerged
coronavirus that infected more than 8000 individuals and resulted
in more than 800 (10–15%) fatalities in 2003. The causative
agent of SARS has been identified as a novel human coronavirus (SARS-CoV),
and its viral protease, SARS-CoV 3CL<sup>pro</sup>, has been shown
to be essential for replication and has hence been recognized as a
potent drug target for SARS infection. Currently, there is no effective
treatment for this epidemic despite the intensive research that has
been undertaken since 2003 (over 3500 publications). This perspective
focuses on the status of various efficacious anti-SARS-CoV 3CL<sup>pro</sup> chemotherapies discovered during the last 12 years (2003–2015)
from all sources, including laboratory synthetic methods, natural
products, and virtual screening. We describe here mainly peptidomimetic
and small molecule inhibitors of SARS-CoV 3CL<sup>pro</sup>. Attempts
have been made to provide a complete description of the structural
features and binding modes of these inhibitors under many conditions.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Cheever, F S" uniqKey="Cheever F">F. S. Cheever</name></author><author><name sortKey="Daniels, J B" uniqKey="Daniels J">J. B. Daniels</name></author><author><name sortKey="Pappenheimer, A M" uniqKey="Pappenheimer A">A. M. Pappenheimer</name></author><author><name sortKey="Baily, O T" uniqKey="Baily O">O. T. Baily</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Bailey, O T" uniqKey="Bailey O">O. T. Bailey</name></author><author><name sortKey="Pappenheimer, A M" uniqKey="Pappenheimer A">A. M. Pappenheimer</name></author><author><name sortKey="Sargent, F" uniqKey="Sargent F">F. Sargent</name></author><author><name sortKey="Cheever, M D" uniqKey="Cheever M">M. D. Cheever</name></author><author><name sortKey="Daniels, J B" uniqKey="Daniels J">J. B. 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Lai</name></author></analytic></biblStruct></listBibl></div1></back></TEI><affiliations><list><country><li>Allemagne</li><li>Corée du Sud</li><li>Japon</li></country></list><tree><country name="Allemagne"><noRegion><name sortKey="Pillaiyar, Thanigaimalai" sort="Pillaiyar, Thanigaimalai" uniqKey="Pillaiyar T" first="Thanigaimalai" last="Pillaiyar">Thanigaimalai Pillaiyar</name></noRegion><name sortKey="Namasivayam, Vigneshwaran" sort="Namasivayam, Vigneshwaran" uniqKey="Namasivayam V" first="Vigneshwaran" last="Namasivayam">Vigneshwaran Namasivayam</name></country><country name="Corée du Sud"><noRegion><name sortKey="Manickam, Manoj" sort="Manickam, Manoj" uniqKey="Manickam M" first="Manoj" last="Manickam">Manoj Manickam</name></noRegion><name sortKey="Jung, Sang Hun" sort="Jung, Sang Hun" uniqKey="Jung S" first="Sang-Hun" last="Jung">Sang-Hun Jung</name></country><country name="Japon"><noRegion><name sortKey="Hayashi, Yoshio" sort="Hayashi, Yoshio" uniqKey="Hayashi Y" first="Yoshio" last="Hayashi">Yoshio Hayashi</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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