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10.1038/s41467-021-22580-8

http://scihub22266oqcxt.onion/10.1038/s41467-021-22580-8
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33863887!8052374!33863887
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suck abstract from ncbi


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pmid33863887      Nat+Commun 2021 ; 12 (1): 2295
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  • Orally delivered MK-4482 inhibits SARS-CoV-2 replication in the Syrian hamster model #MMPMID33863887
  • Rosenke K; Hansen F; Schwarz B; Feldmann F; Haddock E; Rosenke R; Barbian K; Meade-White K; Okumura A; Leventhal S; Hawman DW; Ricotta E; Bosio CM; Martens C; Saturday G; Feldmann H; Jarvis MA
  • Nat Commun 2021[Apr]; 12 (1): 2295 PMID33863887show ga
  • The COVID-19 pandemic progresses unabated in many regions of the world. An effective antiviral against SARS-CoV-2 that could be administered orally for use following high-risk exposure would be of substantial benefit in controlling the COVID-19 pandemic. Herein, we show that MK-4482, an orally administered nucleoside analog, inhibits SARS-CoV-2 replication in the Syrian hamster model. The inhibitory effect of MK-4482 on SARS-CoV-2 replication is observed in animals when the drug is administered either beginning 12 h before or 12 h following infection in a high-risk exposure model. These data support the potential utility of MK-4482 to control SARS-CoV-2 infection in humans following high-risk exposure as well as for treatment of COVID-19 patients.
  • |*COVID-19 Drug Treatment[MESH]
  • |Administration, Oral[MESH]
  • |Animals[MESH]
  • |Antiviral Agents/*administration & dosage[MESH]
  • |COVID-19/virology[MESH]
  • |Chlorocebus aethiops[MESH]
  • |Cytidine/administration & dosage/*analogs & derivatives[MESH]
  • |Disease Models, Animal[MESH]
  • |Humans[MESH]
  • |Hydroxylamines/*administration & dosage[MESH]
  • |Mesocricetus[MESH]
  • |SARS-CoV-2/*drug effects/isolation & purification/physiology[MESH]
  • |Vero Cells[MESH]


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