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10.1021/acs.jmedchem.0c01348

http://scihub22266oqcxt.onion/10.1021/acs.jmedchem.0c01348
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33201699!?!33201699

suck abstract from ncbi

pmid33201699      J+Med+Chem 2020 ; 63 (24): 15371-15388
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  • Triterpenoid-Mediated Inhibition of Virus-Host Interaction: Is Now the Time for Discovering Viral Entry/Release Inhibitors from Nature? #MMPMID33201699
  • Li H; Sun J; Xiao S; Zhang L; Zhou D
  • J Med Chem 2020[Dec]; 63 (24): 15371-15388 PMID33201699show ga
  • Fatal infectious diseases caused by HIV-1, influenza A virus, Ebola virus, and currently pandemic coronavirus highlight the great need for the discovery of antiviral agents in mechanisms different from current viral replication-targeted approaches. Given the critical role of virus-host interactions in the viral life cycle, the development of entry or shedding inhibitors may expand the current repertoire of antiviral agents; the combination of antireplication inhibitors and entry or shedding inhibitors would create a multifaceted drug cocktail with a tandem antiviral mechanism. Therefore, we provide critical information about triterpenoids as potential antiviral agents targeting entry and release, focusing specifically on the emerging aspect of triterpenoid-mediated inhibition of a variety of virus-host membrane fusion mechanisms via a trimer-of-hairpin motif. These properties of triterpenoids supply their host an evolutionary advantage for chemical defense and may protect against an increasingly diverse array of viruses infecting mammals, providing a direction for antiviral drug discovery.
  • |Animals[MESH]
  • |Antiviral Agents/*therapeutic use[MESH]
  • |Cell Line, Tumor[MESH]
  • |Humans[MESH]
  • |Molecular Structure[MESH]
  • |RNA Viruses/*drug effects[MESH]
  • |SARS-CoV-2/drug effects[MESH]
  • |Structure-Activity Relationship[MESH]
  • |Triterpenes/*therapeutic use[MESH]
  • |Virus Internalization/*drug effects[MESH]
  • |Virus Release/*drug effects[MESH]


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