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
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
BO - Biophysics
OECD FORD branch
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Result continuities
Project
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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
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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
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