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α-glucosidase inhibitors as host-directed antiviral agents with potential for the treatment of COVID-19.
Williams, Spencer J; Goddard-Borger, Ethan D.
  • Williams SJ; School of Chemistry and Bio21 Molecular Science and Biotechnology Institute, University of Melbourne, Parkville 3010, Victoria, Australia.
  • Goddard-Borger ED; The Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria 3052, Australia.
Biochem Soc Trans ; 48(3): 1287-1295, 2020 Jun 30.
Article in English | MEDLINE | ID: covidwho-592506
ABSTRACT
The ongoing COVID-19 pandemic, caused by SARS-CoV-2, has pushed the health systems of many countries to breaking point and precipitated social distancing measures that have crippled economic activities across the globe. A return to normality is unlikely until effective therapeutics and a vaccine are available. The immediacy of this problem suggests that drug strategies should focus on repurposing approved drugs or late-stage clinical candidates, as these have the shortest path to use in the clinic. Here, we review and discuss the role of host cell N-glycosylation pathways to virus replication and the drugs available to disrupt these pathways. In particular, we make a case for evaluation of the well-tolerated drugs miglitol, celgosivir and especially miglustat for the treatment of COVID-19.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Pneumonia, Viral / Coronavirus Infections / Drug Repositioning / Glycoside Hydrolase Inhibitors / Betacoronavirus Type of study: Experimental Studies / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Biochem Soc Trans Year: 2020 Document Type: Article Affiliation country: Bst20200505

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Pneumonia, Viral / Coronavirus Infections / Drug Repositioning / Glycoside Hydrolase Inhibitors / Betacoronavirus Type of study: Experimental Studies / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Biochem Soc Trans Year: 2020 Document Type: Article Affiliation country: Bst20200505