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10.3390/molecules25173920

http://scihub22266oqcxt.onion/10.3390/molecules25173920
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32867349!7504761!32867349
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suck abstract from ncbi


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pmid32867349      Molecules 2020 ; 25 (17): ä
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  • Design and Evaluation of Anti-SARS-Coronavirus Agents Based on Molecular Interactions with the Viral Protease #MMPMID32867349
  • Akaji K; Konno H
  • Molecules 2020[Aug]; 25 (17): ä PMID32867349show ga
  • Three types of new coronaviruses (CoVs) have been identified recently as the causative viruses for the severe pneumonia-like respiratory illnesses, severe acute respiratory syndrome (SARS), Middle East respiratory syndrome (MERS), and corona-virus disease 2019 (COVID-19). Neither therapeutic agents nor vaccines have been developed to date, which is a major drawback in controlling the present global pandemic of COVID-19 caused by SARS coronavirus 2 (SARS-CoV-2) and has resulted in more than 20,439,814 cases and 744,385 deaths. Each of the 3C-like (3CL) proteases of the three CoVs is essential for the proliferation of the CoVs, and an inhibitor of the 3CL protease (3CL(pro)) is thought to be an ideal therapeutic agent against SARS, MERS, or COVID-19. Among these, SARS-CoV is the first corona-virus isolated and has been studied in detail since the first pandemic in 2003. This article briefly reviews a series of studies on SARS-CoV, focusing on the development of inhibitors for the SARS-CoV 3CL(pro) based on molecular interactions with the 3CL protease. Our recent approach, based on the structure-based rational design of a novel scaffold for SARS-CoV 3CL(pro) inhibitor, is also included. The achievements summarized in this short review would be useful for the design of a variety of novel inhibitors for corona-viruses, including SARS-CoV-2.
  • |Antiviral Agents/*chemistry/classification/therapeutic use[MESH]
  • |Betacoronavirus/*chemistry/drug effects/enzymology[MESH]
  • |COVID-19[MESH]
  • |Catalytic Domain[MESH]
  • |Coronavirus 3C Proteases[MESH]
  • |Coronavirus Infections/drug therapy[MESH]
  • |Crystallography, X-Ray[MESH]
  • |Cysteine Endopeptidases/chemistry/genetics/metabolism[MESH]
  • |Humans[MESH]
  • |Kinetics[MESH]
  • |Middle East Respiratory Syndrome Coronavirus/genetics/metabolism/*pathogenicity[MESH]
  • |Molecular Docking Simulation[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/drug therapy[MESH]
  • |Protease Inhibitors/*chemistry/classification/therapeutic use[MESH]
  • |Protein Binding[MESH]
  • |Protein Conformation, alpha-Helical[MESH]
  • |Protein Conformation, beta-Strand[MESH]
  • |Protein Interaction Domains and Motifs[MESH]
  • |SARS-CoV-2[MESH]
  • |Severe Acute Respiratory Syndrome/drug therapy[MESH]
  • |Severe acute respiratory syndrome-related coronavirus/genetics/metabolism/*pathogenicity[MESH]
  • |Substrate Specificity[MESH]
  • |Thermodynamics[MESH]


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