Počet záznamů: 1  

Novel trisubstituted acridines as human telomeric quadruplex binding ligands

  1. 1.
    SYSNO ASEP0439913
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevNovel trisubstituted acridines as human telomeric quadruplex binding ligands
    Tvůrce(i) Ungvarsky, J. (SK)
    Plšíková, J. (SK)
    Janovec, J. (SK)
    Koval, J. (SK)
    Mikeš, J. (SK)
    Mikesová, L. (SK)
    Harvanova, D. (SK)
    Fedoročko, P. (SK)
    Kristian, P. (SK)
    Kašpárková, Jana (BFU-R) RID, ORCID
    Brabec, Viktor (BFU-R) RID, ORCID
    Celkový počet autorů18
    Zdroj.dok.Bioorganic Chemistry. - : Elsevier - ISSN 0045-2068
    Roč. 57, DEC 2014 (2014), s. 13-29
    Poč.str.17 s.
    Forma vydáníTištěná - P
    Jazyk dok.eng - angličtina
    Země vyd.US - Spojené státy americké
    Klíč. slovaBraco 19 derivatives ; Trisubstituted acridines ; DNA binding
    Vědní obor RIVBO - Biofyzika
    Institucionální podporaBFU-R - RVO:68081707
    UT WOS000345698000003
    DOI https://doi.org/10.1016/j.bioorg.2014.07.010
    AnotaceA novel series of trisubstituted acridines were synthesized with the aim of mimicking the effects of BRACO-19. These compounds were synthesized by modifying the molecular structure of BRACO19 at positions 3 and 6 with heteroacyclic moieties. All of the derivatives presented in the study exhibited stabilizing effects on the human telomeric DNA quadruplex. UV-vis spectroscopy, circular dichroism, linear dichroism and viscosimetry were used in order to study the nature of the DNA binding in more detail. The results show that all of the novel derivatives were able to fold the single-stranded DNA sequences into antiparallel G-quadruplex structures, with derivative 15 exhibiting the highest stabilizing capability. Cell cycle analysis revealed that a primary trend of the "braco"-like derivatives was to arrest the cells in the Sand G(2)M-phases of the cell cycle within the first 72 h, with derivative 13 and BRACO19 proving particularly effective in suppressing cell proliferation. All studies derivatives were less toxic to human fibroblast cell line in comparison with HT 29 cancer cell line. (C) 2014 Elsevier Inc. All rights reserved.
    PracovištěBiofyzikální ústav
    KontaktJana Poláková, polakova@ibp.cz, Tel.: 541 517 244
    Rok sběru2015
Počet záznamů: 1  

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