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Sketching the historical development of pyrimidones as the inhibitors of the HIV integrase

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F15%3A33157531" target="_blank" >RIV/61989592:15310/15:33157531 - isvavai.cz</a>

  • Alternative codes found

    RIV/61389030:_____/15:00447199

  • Result on the web

    <a href="http://www.sciencedirect.com/science/article/pii/S0223523414006114" target="_blank" >http://www.sciencedirect.com/science/article/pii/S0223523414006114</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.ejmech.2014.07.005" target="_blank" >10.1016/j.ejmech.2014.07.005</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Sketching the historical development of pyrimidones as the inhibitors of the HIV integrase

  • Original language description

    Heterocyclic substances perform a very unique role in drug design and discovery. This article provides the primary objectives of the analysis within pyrimidine centered new heterocyclic elements chronologically from their finding focusing on one of the essential enzyme of HIV virus particle that is integrase upon suppressing its strand transfer function. The class of compounds reviewed here includes bicyclic pyrimidines, dihydroxypyrimidines, pyrimidine-2,4-dinones, N-methylpyrimidones, pyranopyrimidine, pyridine-quinoline conjugates, pyrimidine-2-carboxamides, N-3 hydroxylated pyrimidine-2,4-diones as well as their various substituted analogues. Such initiatives released an effective drug Raltegravir as a first FDA approved anti-HIV integrase inhibitor as well as several of its derivatives along with other pyrimidones is under clinical or preclinical growth. Some of the provided scaffolds indicated dual anti-HIV efficacies against HIV reverse transcriptase and integrase enzymes at bot

  • Czech name

  • Czech description

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

    <a href="/en/project/LO1204" target="_blank" >LO1204: Sustainable development of research in the Centre of the Region Haná</a><br>

  • Continuities

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

Others

  • Publication year

    2015

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    European Journal of Medicinal Chemistry

  • ISSN

    0223-5234

  • e-ISSN

  • Volume of the periodical

    97

  • Issue of the periodical within the volume

    JUN

  • Country of publishing house

    FR - FRANCE

  • Number of pages

    15

  • Pages from-to

    649-663

  • UT code for WoS article

    000356734600047

  • EID of the result in the Scopus database