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Adenosine triphosphate analogs can efficiently inhibit the Zika virus RNA-dependent RNA polymerase

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00027162%3A_____%2F17%3AN0000096" target="_blank" >RIV/00027162:_____/17:N0000096 - isvavai.cz</a>

  • Alternative codes found

    RIV/60077344:_____/17:00474801 RIV/61388963:_____/17:00474801

  • Result on the web

    <a href="http://www.sciencedirect.com/science/article/pii/S0166354216306143" target="_blank" >http://www.sciencedirect.com/science/article/pii/S0166354216306143</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.antiviral.2016.11.020" target="_blank" >10.1016/j.antiviral.2016.11.020</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Adenosine triphosphate analogs can efficiently inhibit the Zika virus RNA-dependent RNA polymerase

  • Original language description

    We describe the expression and purification of an active recombinant Zika virus RNA-dependent RNA polymerase (RdRp). Next, we present the development and optimization of an in vitro assay to measure its activity. We then applied the assay to selected triphosphate analogs and discovered that 2'-C-methylated nucleosides exhibit strong inhibitory activity. Surprisingly, also carbocyclic derivatives with the carbohydrate locked in a North-like conformation as well as a ribonucleotide with a South conformation exhibited strong activity. Our results suggest that the traditional 2'-C-methylated nucleosides pursued in the race for anti-HCV treatment can be superseded by brand new scaffolds in the case of the Zika virus.

  • 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

    10607 - Virology

Result continuities

  • Project

    <a href="/en/project/GA15-09310S" target="_blank" >GA15-09310S: Rational design of phosphatidylinositol 4-kinase IIalpha inhibitors as tools for chemical biology and potential therapeutics</a><br>

  • Continuities

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

Others

  • Publication year

    2017

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Antiviral Research

  • ISSN

    0166-3542

  • e-ISSN

  • Volume of the periodical

  • Issue of the periodical within the volume

    137

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    3

  • Pages from-to

    131-133

  • UT code for WoS article

    000393005300016

  • EID of the result in the Scopus database