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Small molecule-based inhibitors for treatment of tick-borne encephalitis virus infection: Nucleoside analogs and nonnucleoside antivirals

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60077344%3A_____%2F22%3A00569226" target="_blank" >RIV/60077344:_____/22:00569226 - isvavai.cz</a>

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/abs/pii/S0065774322000033?pes=vor" target="_blank" >https://www.sciencedirect.com/science/article/abs/pii/S0065774322000033?pes=vor</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/bs.armc.2022.08.003" target="_blank" >10.1016/bs.armc.2022.08.003</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Small molecule-based inhibitors for treatment of tick-borne encephalitis virus infection: Nucleoside analogs and nonnucleoside antivirals

  • Original language description

    Tick-borne encephalitis (TBE) is one of the most serious neurological infections in Europe and Northeastern Asia. The causative agent of TBE is the tick-borne encephalitis virus (TBEV). Although several effective vaccines are legislated to prevent TBE, there are currently no approved treatments/anti-TBEV drugs other than supportive measures. Therefore, there is an urgent medical need for the development of novel, specific, and effective antivirals to treat patients with TBEV infection. This report summarizes the available information on antiviral research on small molecule-based inhibitors of TBEV replication. The main focus is on the description of nucleoside analogs, a leading group of antiviral compounds with the highest anti-TBEV potency. Various sugar/nucleobase modifications of the nucleoside scaffold that have been made to maximize the antiviral activity and decrease the cytotoxicity of the compounds are discussed. Emphasis is also placed on elucidating the mechanism of action of the inhibitors studied and their relationship to the development of antiviral resistance. Moreover, a brief overview of nonnucleoside inhibitors, natural compounds, repurposed drugs, and synthetic broad-spectrum antivirals is also part of this chapter. The review shows that specific therapies based on small-molecule inhibitors, in combination with effective vaccination strategies, could be effective prophylactic and curative tools to control TBEV infections in humans.

  • Czech name

  • Czech description

Classification

  • Type

    C - Chapter in a specialist book

  • CEP classification

  • OECD FORD branch

    10606 - Microbiology

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2022

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Book/collection name

    Annual Reports in Medicinal Chemistry

  • ISBN

    9780323988933

  • Number of pages of the result

    38

  • Pages from-to

    "Roč. 58 (2022)"

  • Number of pages of the book

    256

  • Publisher name

    Springer

  • Place of publication

    Cham

  • UT code for WoS chapter