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10.3390/v13071220

http://scihub22266oqcxt.onion/10.3390/v13071220
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suck abstract from ncbi


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pmid34202565      Viruses 2021 ; 13 (7): ä
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  • The Antiviral Effect of the Chemical Compounds Targeting DED/EDh Motifs of the Viral Proteins on Lymphocytic Choriomeningitis Virus and SARS-CoV-2 #MMPMID34202565
  • Ngwe Tun MM; Morita K; Ishikawa T; Urata S
  • Viruses 2021[Jun]; 13 (7): ä PMID34202565show ga
  • Arenaviruses and coronaviruses include several human pathogenic viruses, such as Lassa virus, Lymphocytic choriomeningitis virus (LCMV), SARS-CoV, MERS-CoV, and SARS-CoV-2. Although these viruses belong to different virus families, they possess a common motif, the DED/EDh motif, known as an exonuclease (ExoN) motif. In this study, proof-of-concept studies, in which the DED/EDh motif in these viral proteins, NP for arenaviruses, and nsp14 for coronaviruses, could be a drug target, were performed. Docking simulation studies between two structurally different chemical compounds, ATA and PV6R, and the DED/EDh motifs in these viral proteins indicated that these compounds target DED/EDh motifs. The concentration which exhibited modest cell toxicity was used with these compounds to treat LCMV and SARS-CoV-2 infections in two different cell lines, A549 and Vero 76 cells. Both ATA and PV6R inhibited the post-entry step of LCMV and SARS-CoV-2 infection. These studies strongly suggest that DED/EDh motifs in these viral proteins could be a drug target to combat two distinct viral families, arenaviruses and coronaviruses.
  • |A549 Cells[MESH]
  • |Amino Acid Motifs[MESH]
  • |Animals[MESH]
  • |Antiviral Agents/*pharmacology[MESH]
  • |Chlorocebus aethiops[MESH]
  • |Drug Discovery[MESH]
  • |Exoribonucleases/*antagonists & inhibitors[MESH]
  • |Humans[MESH]
  • |Lymphocytic choriomeningitis virus/*drug effects[MESH]
  • |Molecular Docking Simulation[MESH]
  • |SARS-CoV-2/*drug effects[MESH]
  • |Vero Cells[MESH]
  • |Viral Nonstructural Proteins/*antagonists & inhibitors[MESH]
  • |Viral Proteins/*antagonists & inhibitors[MESH]


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