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Review rapamycin: Drug repurposing in sars-cov-2 infection

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dc.rights.license CC BY eng
dc.contributor.author Patocka, J. cze
dc.contributor.author Kuča, Kamil cze
dc.contributor.author Olekšák, Patrik cze
dc.contributor.author Nepovimová, Eugenie cze
dc.contributor.author Valis, M. cze
dc.contributor.author Novotny, M. cze
dc.contributor.author Klimova, B. cze
dc.date.accessioned 2026-07-21T06:18:59Z
dc.date.available 2026-07-21T06:18:59Z
dc.date.issued 2021 eng
dc.identifier.issn 1424-8247 eng
dc.identifier.uri http://hdl.handle.net/20.500.12603/2740
dc.description.abstract Since December 2019, SARS-CoV-2 (COVID-19) has been a worldwide pandemic with enormous consequences for human health and the world economy. Remdesivir is the only drug in the world that has been approved for the treating of COVID-19. This drug, as well as vaccination, still has uncertain effectiveness. Drug repurposing could be a promising strategy how to find an appropriate molecule: rapamycin could be one of them. The authors performed a systematic literature review of available studies on the research describing rapamycin in association with COVID-19 infection. Only peer-reviewed English-written articles from the world’s acknowledged databases Web of Science, PubMed, Springer and Scopus were involved. Five articles were eventually included in the final analysis. The findings indicate that rapamycin seems to be a suitable candidate for drug repurposing. In addition, it may represent a better candidate for COVID-19 therapy than commonly tested antivirals. It is also likely that its efficiency will not be reduced by the high rate of viral RNA mutation. © 2021 by the authors. Licensee MDPI, Basel, Switzerland. eng
dc.format p. "Article number 217" eng
dc.language.iso eng eng
dc.publisher MDPI AG eng
dc.relation.ispartof Pharmaceuticals, volume 14, issue: 3 eng
dc.subject COVID-19 eng
dc.subject MTOR inhibitor eng
dc.subject Rapamycin eng
dc.subject SARS-CoV-19 eng
dc.subject Sirolimus eng
dc.title Review rapamycin: Drug repurposing in sars-cov-2 infection eng
dc.type article eng
dc.identifier.obd 43877580 eng
dc.identifier.doi 10.3390/ph14030217 eng
dc.publicationstatus postprint eng
dc.peerreviewed yes eng
dc.source.url https://www.mdpi.com/1424-8247/14/3/217 cze
dc.relation.publisherversion https://www.mdpi.com/1424-8247/14/3/217 eng
dc.rights.access Open Access eng


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