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α-glucosidase inhibitors as host-directed antiviral agents with potential for the treatment of COVID-19

Spencer J. Williams, Ethan D. Goddard‐Borger

2020Biochemical Society Transactions70 citationsDOIOpen Access PDF

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.

Topics & Concepts

Coronavirus disease 2019 (COVID-19)ImmediacyRepurposingDrug repositioningPandemicViral replicationMedicineVirologyPharmacologyBiologyDrugVirusInternal medicineDiseaseInfectious disease (medical specialty)PhilosophyEcologyEpistemologySARS-CoV-2 and COVID-19 ResearchCalcium signaling and nucleotide metabolismMosquito-borne diseases and control
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