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Nucleoside analogs as a rich source of antiviral agents active against arthropod-borne flaviviruses

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00027162%3A_____%2F18%3AN0000061" target="_blank" >RIV/00027162:_____/18:N0000061 - isvavai.cz</a>

  • Result on the web

    <a href="http://journals.sagepub.com/doi/10.1177/2040206618761299" target="_blank" >http://journals.sagepub.com/doi/10.1177/2040206618761299</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1177/2040206618761299" target="_blank" >10.1177/2040206618761299</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Nucleoside analogs as a rich source of antiviral agents active against arthropod-borne flaviviruses

  • Original language description

    Nucleoside analogs represent the largest class of small molecule-based antivirals, which currently form the backbone of chemotherapy of chronic infections caused by HIV, hepatitis B or C viruses, and herpes viruses. High antiviral potency and favorable pharmacokinetics parameters make some nucleoside analogs suitable also for the treatment of acute infections caused by other medically important RNA and DNA viruses. This review summarizes available information on antiviral research of nucleoside analogs against arthropod-borne members of the genus Flavivirus within the family Flaviviridae, being primarily focused on description of nucleoside inhibitors of flaviviral RNA-dependent RNA polymerase, methyltransferase, and helicase/NTPase. Inhibitors of intracellular nucleoside synthesis and newly discovered nucleoside derivatives with high antiflavivirus potency, whose modes of action are currently not completely understood, have drawn attention. Moreover, this review highlights important challenges and complications in nucleoside analog development and suggests possible strategies to overcome these limitations.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>SC</sub> - Article in a specialist periodical, which is included in the SCOPUS database

  • CEP classification

  • OECD FORD branch

    10607 - Virology

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2018

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Antiviral Chemistry and Chemotherapy

  • ISSN

    2040-2066

  • e-ISSN

  • Volume of the periodical

    26

  • Issue of the periodical within the volume

    March

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    28

  • Pages from-to

    2040206618761299

  • UT code for WoS article

  • EID of the result in the Scopus database

    2-s2.0-85045317817