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Viral proteases as therapeutic targets

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    0565334 - ÚOCHB 2023 RIV NL eng J - Journal Article
    Majerová, Taťána - Konvalinka, Jan
    Viral proteases as therapeutic targets.
    Molecular Aspects of Medicine. Roč. 88, December (2022), č. článku 101159. ISSN 0098-2997. E-ISSN 1872-9452
    R&D Projects: GA MŠMT(CZ) LX22NPO5103
    Institutional support: RVO:61388963
    Keywords : hepatitis C virus * human immunodeficiency virus * orally bioavailable inhibitor
    OECD category: Virology
    Impact factor: 10.6, year: 2022
    Method of publishing: Open access
    https://doi.org/10.1016/j.mam.2022.101159

    Some medically important viruses―including retroviruses, flaviviruses, coronaviruses, and herpesviruses―code for a protease, which is indispensable for viral maturation and pathogenesis. Viral protease inhibitors have become an important class of antiviral drugs. Development of the first-in-class viral protease inhibitor saquinavir, which targets HIV protease, started a new era in the treatment of chronic viral diseases. Combining several drugs that target different steps of the viral life cycle enables use of lower doses of individual drugs (and thereby reduction of potential side effects, which frequently occur during long term therapy) and reduces drug-resistance development. Currently, several HIV and HCV protease inhibitors are routinely used in clinical practice. In addition, a drug including an inhibitor of SARS-CoV-2 main protease, nirmatrelvir (co-administered with a pharmacokinetic booster ritonavir as Paxlovid®), was recently authorized for emergency use. This review summarizes the basic features of the proteases of human immunodeficiency virus (HIV), hepatitis C virus (HCV), and SARS-CoV-2 and discusses the properties of their inhibitors in clinical use, as well as development of compounds in the pipeline.
    Permanent Link: https://hdl.handle.net/11104/0336883

     
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    10.1016j.mam.2022.101159.pdf48.1 MBPublisher’s postprintopen-access
     
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