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10.1042/BST20200505

http://scihub22266oqcxt.onion/10.1042/BST20200505
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32510142!ä!32510142

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suck abstract from ncbi


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pmid32510142      Biochem+Soc+Trans 2020 ; 48 (3): 1287-1295
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  • alpha-glucosidase inhibitors as host-directed antiviral agents with potential for the treatment of COVID-19 #MMPMID32510142
  • Williams SJ; Goddard-Borger ED
  • Biochem Soc Trans 2020[Jun]; 48 (3): 1287-1295 PMID32510142show ga
  • 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.
  • |Antiviral Agents/*pharmacology/therapeutic use[MESH]
  • |Betacoronavirus/*chemistry[MESH]
  • |COVID-19[MESH]
  • |Calnexin/metabolism[MESH]
  • |Coronavirus Infections/drug therapy/*metabolism/virology[MESH]
  • |Drug Repositioning/*methods[MESH]
  • |Glycoside Hydrolase Inhibitors/*pharmacology/therapeutic use[MESH]
  • |Glycosylation/drug effects[MESH]
  • |Host-Pathogen Interactions[MESH]
  • |Humans[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/drug therapy/*metabolism/virology[MESH]
  • |Protein Folding/drug effects[MESH]
  • |SARS-CoV-2[MESH]
  • |Spike Glycoprotein, Coronavirus/metabolism[MESH]
  • |Virus Replication/drug effects[MESH]


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