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Antiviral activity of triazine analogues of 1- (S)-[3-hydroxy-2-(phosphonomethoxy)propyl]cytosine (Cidofovir) and related compounds

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F07%3A00081024" target="_blank" >RIV/61388963:_____/07:00081024 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Antiviral activity of triazine analogues of 1- (S)-[3-hydroxy-2-(phosphonomethoxy)propyl]cytosine (Cidofovir) and related compounds

  • Original language description

    Acyclic nucleoside phosphonates containing 5-aza and 6-azacytosine base moiety were synthesized and tested for antiviral activity. The most active compound, 1-(S)-[3-hydroxy-2-(phosphonomethoxy)propyl]-5-azacytosine exerted strong activity against broadspectrum of DNA viruses (adenovirus, poxviruses and herpesviruses).

  • Czech name

    Protivirová aktivita triazinových analogů 1-(S)-[3-hydroxy-2-(phosphonomethoxy)propyl]cytosinu (cidofoviru) a příbuzných sloučenin

  • Czech description

    Byly syntetizovány acyklické nukleosidové fosfonáty obsahující jako bazickou komponentu 5-aza a 6-azacytosin a testována jejich protivirová aktivita. Nejvíce aktivní látka, 1-(S)-[3-hydroxy-2-(phosphonomethoxy)propyl]-5-azacytosin, vykazovala silnou aktivitu proti širokému spektru DNA virů (adenoviry, poxviry a herpesviry).

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CC - Organic chemistry

  • OECD FORD branch

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)<br>Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2007

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Journal of Medicinal Chemistry

  • ISSN

    0022-2623

  • e-ISSN

  • Volume of the periodical

    50

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    9

  • Pages from-to

    1069-1077

  • UT code for WoS article

  • EID of the result in the Scopus database