Serveur d'exploration SRAS

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Nucleoside analogues for the treatment of coronavirus infections

Identifieur interne : 003050 ( Ncbi/Merge ); précédent : 003049; suivant : 003051

Nucleoside analogues for the treatment of coronavirus infections

Auteurs : Andrea J. Pruijssers [États-Unis] ; Mark R. Denison [États-Unis]

Source :

RBID : PMC:7102703

Descripteurs français

English descriptors

Abstract

Highlights

Coronaviruses (CoV) represent current and future risk for pandemic zoonotic infections.

Nucleoside analogues are highly active across multiple virus families.

CoVs encode a proofreading exoribonuclease that opposes inhibition by many nucleoside analogues.

Remdesivir is an adenosine analogue that acts against a broad spectrum of CoVs.

Other nucleoside analogues show promise against CoVs.


Url:
DOI: 10.1016/j.coviro.2019.04.002
PubMed: 31125806
PubMed Central: 7102703

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Links to Exploration step

PMC:7102703

Le document en format XML

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<p id="par0005">Coronaviruses (CoV) represent current and future risk for pandemic zoonotic infections.</p>
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<p id="par0015">CoVs encode a proofreading exoribonuclease that opposes inhibition by many nucleoside analogues.</p>
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<p id="par0020">Remdesivir is an adenosine analogue that acts against a broad spectrum of CoVs.</p>
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<idno type="ISSN">1879-6257</idno>
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<title>Highlights</title>
<p>
<list list-type="simple" id="lis0005">
<list-item id="lsti0005">
<label></label>
<p id="par0005">Coronaviruses (CoV) represent current and future risk for pandemic zoonotic infections.</p>
</list-item>
<list-item id="lsti0010">
<label></label>
<p id="par0010">Nucleoside analogues are highly active across multiple virus families.</p>
</list-item>
<list-item id="lsti0015">
<label></label>
<p id="par0015">CoVs encode a proofreading exoribonuclease that opposes inhibition by many nucleoside analogues.</p>
</list-item>
<list-item id="lsti0020">
<label></label>
<p id="par0020">Remdesivir is an adenosine analogue that acts against a broad spectrum of CoVs.</p>
</list-item>
<list-item id="lsti0025">
<label></label>
<p id="par0025">Other nucleoside analogues show promise against CoVs.</p>
</list-item>
</list>
</p>
</div>
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<keywords scheme="MESH" qualifier="virologie" xml:lang="fr">
<term>Infections à coronavirus</term>
</keywords>
<keywords scheme="MESH" qualifier="virology" xml:lang="en">
<term>Coronavirus Infections</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Animals</term>
<term>Drug Therapy, Combination</term>
<term>Humans</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Animaux</term>
<term>Association de médicaments</term>
<term>Coronavirus</term>
<term>Coronavirus du syndrome respiratoire du Moyen-Orient</term>
<term>Humains</term>
<term>Réplication virale</term>
<term>Virus du SRAS</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Recent outbreaks of SARS-Coronavirus and MERS-Coronavirus (CoV) have heightened awareness about the lack of vaccines or antiviral compounds approved for prevention or treatment of human or potential zoonotic CoVs. Anti-CoV drug development has long been challenged by the activity of a 3' to 5' proofreading exoribonuclease unique to CoVs. Recently, a promising nucleoside analogue with broad-spectrum activity against CoVs has been identified. This review will discuss progress made in the development of antiviral nucleoside and nucleotide analogues targeting viral RNA synthesis as effective therapeutics against CoV infections and propose promising strategies for combination therapy.</div>
</front>
</TEI>
</pubmed>
</double>
</record>

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