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suck abstract from ncbi


10.1016/j.micpath.2020.104586

http://scihub22266oqcxt.onion/10.1016/j.micpath.2020.104586
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33091582!7573633!33091582
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suck abstract from ncbi

pmid33091582      Microb+Pathog 2020 ; 149 (?): 104586
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  • Inhibition of N-linked Glycosylation by Tunicamycin May Contribute to The Treatment of SARS-CoV-2 #MMPMID33091582
  • Dawood AA; Altobje MA
  • Microb Pathog 2020[Dec]; 149 (?): 104586 PMID33091582show ga
  • SARS-CoV-2 remains a medical and economic challenge, due to the lack of a suitable drug or vaccine. The glycans in some proteins play a pivotal role in protein folding, oligomerization, quality control, sorting, and transport so the hindering of N-linked glycosylation of glycoproteins will prevent assembly of the virion. Tunicamycin an anticancer drug inhibit the N- linked glycans. Our study aimed to find out the mechanism action of tunicamycin on the viral glycoproteins. The growth of coronavirus in the presence inhibitor tunicamycin resulted in the production of spikeless, non-infectious virions which were devoid of S protein. We concluded that tunicamycin inhibits E2, S, and M glycoproteins of coronaviruses. Tunicamycin is also diminished glycosylation of PTMs such as HE, and 8 ab of SARS-CoV. Finally, we recommend using this drug to treat the SARS-CoV-2.
  • |*COVID-19 Drug Treatment[MESH]
  • |Animals[MESH]
  • |COVID-19/metabolism[MESH]
  • |Glycosylation/drug effects[MESH]
  • |Humans[MESH]
  • |SARS-CoV-2/*drug effects/metabolism[MESH]
  • |Spike Glycoprotein, Coronavirus/metabolism[MESH]
  • |Tunicamycin/*pharmacology[MESH]


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