Number of the records: 1  

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

  1. 1.
    SYSNO ASEP0447199
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleSketching the historical development of pyrimidones as the inhibitors of the HIV integrase
    Author(s) Patel, Rahul V. (UEB-Q)
    Keum, Y.S. (KR)
    Park, S.W. (KR)
    Source TitleEuropean Journal of Medicinal Chemistry. - : Elsevier - ISSN 0223-5234
    Roč. 97, JUN 5 (2015), s. 649-663
    Number of pages15 s.
    Languageeng - English
    CountryFR - France
    KeywordsPyrimidones ; Anti-HIV ; Integrase inhibitors
    Subject RIVCE - Biochemistry
    Institutional supportUEB-Q - RVO:61389030
    UT WOS000356734600047
    DOI10.1016/j.ejmech.2014.07.005
    AnnotationHeterocyclic 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 both cites as 3'-processing and strand transfer, while several scaffolds exhibited potency against Raltegravir resistant HIV mutant strains determining themselves a potent class of compounds having appealing upcoming implementations. Connections of the new compounds' molecular structure and HIV viral target has been overviewed to be able to accomplish further growth of promising anti-HIV agents in future drug discovery process.
    WorkplaceInstitute of Experimental Botany
    ContactDavid Klier, knihovna@ueb.cas.cz, Tel.: 220 390 469
    Year of Publishing2016
Number of the records: 1  

  This site uses cookies to make them easier to browse. Learn more about how we use cookies.