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10.3390/pathogens9050320

http://scihub22266oqcxt.onion/10.3390/pathogens9050320
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32357471!7281371!32357471
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suck abstract from ncbi


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pmid32357471      Pathogens 2020 ; 9 (5): ä
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  • Feasibility of Known RNA Polymerase Inhibitors as Anti-SARS-CoV-2 Drugs #MMPMID32357471
  • Neogi U; Hill KJ; Ambikan AT; Heng X; Quinn TP; Byrareddy SN; Sonnerborg A; Sarafianos SG; Singh K
  • Pathogens 2020[Apr]; 9 (5): ä PMID32357471show ga
  • Coronaviruses (CoVs) are positive-stranded RNA viruses that infect humans and animals. Infection by CoVs such as HCoV-229E, -NL63, -OC43 and -HKU1 leads to the common cold, short lasting rhinitis, cough, sore throat and fever. However, CoVs such as Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV), Middle East Respiratory Syndrome Coronavirus (MERS-CoV), and the newest SARS-CoV-2 (the causative agent of COVID-19) lead to severe and deadly diseases with mortality rates ranging between ~1 to 35% depending on factors such as age and pre-existing conditions. Despite continuous global health threats to humans, there are no approved vaccines or drugs targeting human CoVs, and the recent outbreak of COVID-19 emphasizes an urgent need for therapeutic interventions. Using computational and bioinformatics tools, here we present the feasibility of reported broad-spectrum RNA polymerase inhibitors as anti- SARS-CoV-2 drugs targeting its main RNA polymerase, suggesting that investigational and approved nucleoside RNA polymerase inhibitors have potential as anti-SARS-CoV-2 drugs. However, we note that it is also possible for SARS-CoV-2 to evolve and acquire drug resistance mutations against these nucleoside inhibitors.
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