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10.1016/j.antiviral.2021.105075

http://scihub22266oqcxt.onion/10.1016/j.antiviral.2021.105075
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33872675!8052511!33872675
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suck abstract from ncbi


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pmid33872675      Antiviral+Res 2021 ; 190 (ä): 105075
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  • Discovery of chebulagic acid and punicalagin as novel allosteric inhibitors of SARS-CoV-2 3CL(pro) #MMPMID33872675
  • Du R; Cooper L; Chen Z; Lee H; Rong L; Cui Q
  • Antiviral Res 2021[Jun]; 190 (ä): 105075 PMID33872675show ga
  • The emerging SARS-CoV-2 infection is the cause of the global COVID-19 pandemic. To date, there are limited therapeutic options available to fight this disease. Here we examined the inhibitory abilities of two broad-spectrum antiviral natural products chebulagic acid (CHLA) and punicalagin (PUG) against SARS-CoV-2 viral replication. Both CHLA and PUG reduced virus-induced plaque formation in Vero-E6 monolayer at noncytotoxic concentrations, by targeting the enzymatic activity of viral 3-chymotrypsin-like cysteine protease (3CL(pro)) as allosteric regulators. Our study demonstrates the potential use of CHLA and PUG as novel COVID-19 therapies.
  • |Allosteric Site[MESH]
  • |Animals[MESH]
  • |Antiviral Agents/chemistry/*pharmacology[MESH]
  • |Benzopyrans/chemistry/*pharmacology[MESH]
  • |COVID-19 Drug Treatment[MESH]
  • |COVID-19/virology[MESH]
  • |Chlorocebus aethiops[MESH]
  • |Coronavirus 3C Proteases/*antagonists & inhibitors/chemistry/metabolism[MESH]
  • |Drug Discovery[MESH]
  • |Glucosides/chemistry/*pharmacology[MESH]
  • |Hydrolyzable Tannins/*pharmacology[MESH]
  • |Molecular Docking Simulation[MESH]
  • |Protease Inhibitors/pharmacology[MESH]
  • |SARS-CoV-2/*drug effects/metabolism[MESH]
  • |Vero Cells[MESH]


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