Recent developments on coronavirus main protease/3C like protease inhibitors.
Identifieur interne : 001165 ( PubMed/Corpus ); précédent : 001164; suivant : 001166Recent developments on coronavirus main protease/3C like protease inhibitors.
Auteurs : Qi Zhao ; Erin Weber ; Haitao YangSource :
- Recent patents on anti-infective drug discovery [ 2212-4071 ] ; 2013.
English descriptors
- KwdEn :
- Crystallography, X-Ray, Cysteine Endopeptidases (chemistry), Cysteine Endopeptidases (metabolism), Drug Design, Drug Evaluation, Preclinical (methods), Humans, Molecular Structure, Patents as Topic, Protease Inhibitors (chemistry), Protease Inhibitors (pharmacology), Severe Acute Respiratory Syndrome (virology).
- MESH :
- chemical , chemistry : Cysteine Endopeptidases, Protease Inhibitors.
- chemical , metabolism : Cysteine Endopeptidases.
- methods : Drug Evaluation, Preclinical.
- chemical , pharmacology : Protease Inhibitors.
- virology : Severe Acute Respiratory Syndrome.
- Crystallography, X-Ray, Drug Design, Humans, Molecular Structure, Patents as Topic.
Abstract
Coronaviruses have been thrust into the spotlight by the recurring novel human coronavirus infections following the 2003 SARS pandemic. In the years since the initial SARS outbreak, the arsenal to fight this virus family has been significantly increased by the rapid growth of coronavirus research. Among the potential viral drug targets, coronavirus 3C like proteases (3Cl) have emerged as the most popular drug target. A number of patented inhibitors with promising clinical potential have been developed via different methods of drug discovery, including virtual screening, natural product isolation and structure assisted rational drug design. This review serves as a summary of the progress in both the method of drug discovery and the related inhibitors against the coronavirus 3Cl protease.
DOI: 10.2174/1574891x113089990017
PubMed: 23879823
Links to Exploration step
pubmed:23879823Le document en format XML
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<author><name sortKey="Zhao, Qi" sort="Zhao, Qi" uniqKey="Zhao Q" first="Qi" last="Zhao">Qi Zhao</name>
<affiliation><nlm:affiliation>Department of Molecular Biophysics and Biochemistry, Yale University School of Medicine, New Haven, CT 06520, USA. qi.zhao@yale.edu</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Weber, Erin" sort="Weber, Erin" uniqKey="Weber E" first="Erin" last="Weber">Erin Weber</name>
</author>
<author><name sortKey="Yang, Haitao" sort="Yang, Haitao" uniqKey="Yang H" first="Haitao" last="Yang">Haitao Yang</name>
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<author><name sortKey="Weber, Erin" sort="Weber, Erin" uniqKey="Weber E" first="Erin" last="Weber">Erin Weber</name>
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<author><name sortKey="Yang, Haitao" sort="Yang, Haitao" uniqKey="Yang H" first="Haitao" last="Yang">Haitao Yang</name>
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<series><title level="j">Recent patents on anti-infective drug discovery</title>
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<term>Drug Design</term>
<term>Drug Evaluation, Preclinical (methods)</term>
<term>Humans</term>
<term>Molecular Structure</term>
<term>Patents as Topic</term>
<term>Protease Inhibitors (chemistry)</term>
<term>Protease Inhibitors (pharmacology)</term>
<term>Severe Acute Respiratory Syndrome (virology)</term>
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<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Cysteine Endopeptidases</term>
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<front><div type="abstract" xml:lang="en">Coronaviruses have been thrust into the spotlight by the recurring novel human coronavirus infections following the 2003 SARS pandemic. In the years since the initial SARS outbreak, the arsenal to fight this virus family has been significantly increased by the rapid growth of coronavirus research. Among the potential viral drug targets, coronavirus 3C like proteases (3Cl) have emerged as the most popular drug target. A number of patented inhibitors with promising clinical potential have been developed via different methods of drug discovery, including virtual screening, natural product isolation and structure assisted rational drug design. This review serves as a summary of the progress in both the method of drug discovery and the related inhibitors against the coronavirus 3Cl protease. </div>
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<Title>Recent patents on anti-infective drug discovery</Title>
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<ArticleTitle>Recent developments on coronavirus main protease/3C like protease inhibitors.</ArticleTitle>
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<Abstract><AbstractText>Coronaviruses have been thrust into the spotlight by the recurring novel human coronavirus infections following the 2003 SARS pandemic. In the years since the initial SARS outbreak, the arsenal to fight this virus family has been significantly increased by the rapid growth of coronavirus research. Among the potential viral drug targets, coronavirus 3C like proteases (3Cl) have emerged as the most popular drug target. A number of patented inhibitors with promising clinical potential have been developed via different methods of drug discovery, including virtual screening, natural product isolation and structure assisted rational drug design. This review serves as a summary of the progress in both the method of drug discovery and the related inhibitors against the coronavirus 3Cl protease. </AbstractText>
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<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Zhao</LastName>
<ForeName>Qi</ForeName>
<Initials>Q</Initials>
<AffiliationInfo><Affiliation>Department of Molecular Biophysics and Biochemistry, Yale University School of Medicine, New Haven, CT 06520, USA. qi.zhao@yale.edu</Affiliation>
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<Author ValidYN="Y"><LastName>Yang</LastName>
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</Chemical>
<Chemical><RegistryNumber>EC 3.4.22.-</RegistryNumber>
<NameOfSubstance UI="C099456">3C-like proteinase, Coronavirus</NameOfSubstance>
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<Chemical><RegistryNumber>EC 3.4.22.-</RegistryNumber>
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