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Novel trisubstituted acridines as human telomeric quadruplex binding ligands

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68081707%3A_____%2F14%3A00439913" target="_blank" >RIV/68081707:_____/14:00439913 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.bioorg.2014.07.010" target="_blank" >http://dx.doi.org/10.1016/j.bioorg.2014.07.010</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.bioorg.2014.07.010" target="_blank" >10.1016/j.bioorg.2014.07.010</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Novel trisubstituted acridines as human telomeric quadruplex binding ligands

  • Original language description

    A 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 primarytrend 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 d

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    BO - Biophysics

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2014

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Bioorganic Chemistry

  • ISSN

    0045-2068

  • e-ISSN

  • Volume of the periodical

    57

  • Issue of the periodical within the volume

    DEC 2014

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    17

  • Pages from-to

    13-29

  • UT code for WoS article

    000345698000003

  • EID of the result in the Scopus database