Emetine, Ipecac, Ipecac Alkaloids and Analogues as Potential Antiviral Agents for Coronaviruses.
Identifieur interne : 000205 ( Main/Exploration ); précédent : 000204; suivant : 000206Emetine, Ipecac, Ipecac Alkaloids and Analogues as Potential Antiviral Agents for Coronaviruses.
Auteurs : Martin D. Bleasel [Australie] ; Gregory M. Peterson [Australie]Source :
- Pharmaceuticals (Basel, Switzerland) [ 1424-8247 ] ; 2020.
Abstract
The COVID-19 coronavirus is currently spreading around the globe with limited treatment options available. This article presents the rationale for potentially using old drugs (emetine, other ipecac alkaloids or analogues) that have been used to treat amoebiasis in the treatment of COVID-19. Emetine had amongst the lowest reported half-maximal effective concentration (EC50) from over 290 agents screened for the Middle East respiratory syndrome (MERS) and severe acute respiratory syndrome (SARS) coronaviruses. While EC50 concentrations of emetine are achievable in the blood, studies show that concentrations of emetine can be almost 300 times higher in the lungs. Furthermore, based on the relative EC50s of emetine towards the coronaviruses compared with Entamoeba histolytica, emetine could be much more effective as an anti-coronavirus agent than it is against amoebiasis. This paper also discusses the known side effects of emetine and related compounds, how those side effects can be managed, and the optimal method of administration for the potential treatment of COVID-19. Given the serious and immediate threat that the COVID-19 coronavirus poses, our long history with emetine and the likely ability of emetine to reach therapeutic concentrations within the lungs, ipecac, emetine, and other analogues should be considered as potential treatment options, especially if in vitro studies confirm viral sensitivity.
DOI: 10.3390/ph13030051
PubMed: 32245264
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 000092
- to stream PubMed, to step Curation: 000092
- to stream PubMed, to step Checkpoint: 000211
- to stream Ncbi, to step Merge: 002697
- to stream Ncbi, to step Curation: 002697
- to stream Ncbi, to step Checkpoint: 002697
- to stream Main, to step Merge: 000208
- to stream Main, to step Curation: 000205
Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Emetine, Ipecac, Ipecac Alkaloids and Analogues as Potential Antiviral Agents for Coronaviruses.</title>
<author><name sortKey="Bleasel, Martin D" sort="Bleasel, Martin D" uniqKey="Bleasel M" first="Martin D" last="Bleasel">Martin D. Bleasel</name>
<affiliation wicri:level="1"><nlm:affiliation>School of Pharmacy and Pharmacology, University of Tasmania, Hobart Tasmania 7001, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>School of Pharmacy and Pharmacology, University of Tasmania, Hobart Tasmania 7001</wicri:regionArea>
<wicri:noRegion>Hobart Tasmania 7001</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Peterson, Gregory M" sort="Peterson, Gregory M" uniqKey="Peterson G" first="Gregory M" last="Peterson">Gregory M. Peterson</name>
<affiliation wicri:level="1"><nlm:affiliation>School of Pharmacy and Pharmacology, University of Tasmania, Hobart Tasmania 7001, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>School of Pharmacy and Pharmacology, University of Tasmania, Hobart Tasmania 7001</wicri:regionArea>
<wicri:noRegion>Hobart Tasmania 7001</wicri:noRegion>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="2020">2020</date>
<idno type="RBID">pubmed:32245264</idno>
<idno type="pmid">32245264</idno>
<idno type="doi">10.3390/ph13030051</idno>
<idno type="wicri:Area/PubMed/Corpus">000092</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">000092</idno>
<idno type="wicri:Area/PubMed/Curation">000092</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">000092</idno>
<idno type="wicri:Area/PubMed/Checkpoint">000211</idno>
<idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">000211</idno>
<idno type="wicri:Area/Ncbi/Merge">002697</idno>
<idno type="wicri:Area/Ncbi/Curation">002697</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">002697</idno>
<idno type="wicri:doubleKey">1424-8247:2020:Bleasel M:emetine:ipecac:ipecac</idno>
<idno type="wicri:Area/Main/Merge">000208</idno>
<idno type="wicri:Area/Main/Curation">000205</idno>
<idno type="wicri:Area/Main/Exploration">000205</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en">Emetine, Ipecac, Ipecac Alkaloids and Analogues as Potential Antiviral Agents for Coronaviruses.</title>
<author><name sortKey="Bleasel, Martin D" sort="Bleasel, Martin D" uniqKey="Bleasel M" first="Martin D" last="Bleasel">Martin D. Bleasel</name>
<affiliation wicri:level="1"><nlm:affiliation>School of Pharmacy and Pharmacology, University of Tasmania, Hobart Tasmania 7001, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>School of Pharmacy and Pharmacology, University of Tasmania, Hobart Tasmania 7001</wicri:regionArea>
<wicri:noRegion>Hobart Tasmania 7001</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Peterson, Gregory M" sort="Peterson, Gregory M" uniqKey="Peterson G" first="Gregory M" last="Peterson">Gregory M. Peterson</name>
<affiliation wicri:level="1"><nlm:affiliation>School of Pharmacy and Pharmacology, University of Tasmania, Hobart Tasmania 7001, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>School of Pharmacy and Pharmacology, University of Tasmania, Hobart Tasmania 7001</wicri:regionArea>
<wicri:noRegion>Hobart Tasmania 7001</wicri:noRegion>
</affiliation>
</author>
</analytic>
<series><title level="j">Pharmaceuticals (Basel, Switzerland)</title>
<idno type="ISSN">1424-8247</idno>
<imprint><date when="2020" type="published">2020</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass></textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">The COVID-19 coronavirus is currently spreading around the globe with limited treatment options available. This article presents the rationale for potentially using old drugs (emetine, other ipecac alkaloids or analogues) that have been used to treat amoebiasis in the treatment of COVID-19. Emetine had amongst the lowest reported half-maximal effective concentration (EC<sub>50</sub>
) from over 290 agents screened for the Middle East respiratory syndrome (MERS) and severe acute respiratory syndrome (SARS) coronaviruses. While EC<sub>50</sub>
concentrations of emetine are achievable in the blood, studies show that concentrations of emetine can be almost 300 times higher in the lungs. Furthermore, based on the relative EC<sub>50</sub>
s of emetine towards the coronaviruses compared with <i>Entamoeba histolytica</i>
, emetine could be much more effective as an anti-coronavirus agent than it is against amoebiasis. This paper also discusses the known side effects of emetine and related compounds, how those side effects can be managed, and the optimal method of administration for the potential treatment of COVID-19. Given the serious and immediate threat that the COVID-19 coronavirus poses, our long history with emetine and the likely ability of emetine to reach therapeutic concentrations within the lungs, ipecac, emetine, and other analogues should be considered as potential treatment options, especially if in vitro studies confirm viral sensitivity.</div>
</front>
</TEI>
<affiliations><list><country><li>Australie</li>
</country>
</list>
<tree><country name="Australie"><noRegion><name sortKey="Bleasel, Martin D" sort="Bleasel, Martin D" uniqKey="Bleasel M" first="Martin D" last="Bleasel">Martin D. Bleasel</name>
</noRegion>
<name sortKey="Peterson, Gregory M" sort="Peterson, Gregory M" uniqKey="Peterson G" first="Gregory M" last="Peterson">Gregory M. Peterson</name>
</country>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Sante/explor/MersV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000205 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 000205 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Sante |area= MersV1 |flux= Main |étape= Exploration |type= RBID |clé= pubmed:32245264 |texte= Emetine, Ipecac, Ipecac Alkaloids and Analogues as Potential Antiviral Agents for Coronaviruses. }}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i -Sk "pubmed:32245264" \ | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd \ | NlmPubMed2Wicri -a MersV1
This area was generated with Dilib version V0.6.33. |