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Could 5′-N and S ProTide analogues work as prodrugs of antiviral agents?

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00027162%3A_____%2F20%3AN0000015" target="_blank" >RIV/00027162:_____/20:N0000015 - isvavai.cz</a>

  • Alternative codes found

    RIV/60077344:_____/20:00519335 RIV/61388963:_____/20:00519335

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S0960894X19308753?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0960894X19308753?via%3Dihub</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.bmcl.2019.126897" target="_blank" >10.1016/j.bmcl.2019.126897</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Could 5′-N and S ProTide analogues work as prodrugs of antiviral agents?

  • Original language description

    The nucleoside/nucleotide derived antiviral agents have been the most important components of antiviral therapy used in clinics. Recently, the focus of the medicinal chemists within this exciting research field has been affected mainly by the lack of effective therapies for the Hepatitis C virus (HCV) infection and several other “neglected” diseases caused by viruses such as Zika or Dengue. 2′-Methyl modified nucleosides and their monophosphate prodrugs (ProTides) have revolutionized the therapies for HCV in the last few years and, according to the latest research efforts, have also brought a promise for treatment of diseases caused by other members of Flaviviridae family. Here, we report on the design and synthesis of 5’-N and S modified ProTides derived from 2′-methyladenosine. We studied potential applicability of these derivatives as prodrugs of this archetypal antiviral compound.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10613 - Zoology

Result continuities

  • Project

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

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2020

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS

  • ISSN

    0960-894X

  • e-ISSN

    1464-3405

  • Volume of the periodical

    30

  • Issue of the periodical within the volume

    4

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    4

  • Pages from-to

    126897

  • UT code for WoS article

    000507987200013

  • EID of the result in the Scopus database

    2-s2.0-85077142100