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Interaction of cholinesterase modulators with DNA and their cytotoxic activity

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00179906%3A_____%2F14%3A10209873" target="_blank" >RIV/00179906:_____/14:10209873 - isvavai.cz</a>

  • Alternative codes found

    RIV/62690094:18470/14:50002324

  • Result on the web

    <a href="http://www.sciencedirect.com/science/article/pii/S0141813013006314" target="_blank" >http://www.sciencedirect.com/science/article/pii/S0141813013006314</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.ijbiomac.2013.11.022" target="_blank" >10.1016/j.ijbiomac.2013.11.022</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Interaction of cholinesterase modulators with DNA and their cytotoxic activity

  • Original language description

    This research was focused on a study of the binding properties of a series of cholinesterase reactiva-tors compounds K075 (1), K027 (2) and inhibitors compounds K524, K009 and 7-MEOTA (3-5) with calfthymus DNA. The nature of the interactions between compounds 1-5 and DNA were studied using spec-troscopic techniques (UV-vis, fluorescence spectroscopy and circular dichroism). The binding constantsfor complexes of cholinesterase modulators with DNA were determined from UV-vis spectroscopic titra-tions (K =0.5 x 104-8.9 x 105MMINUS SIGN 1). The ability of the prepared analogues to relax topoisomerase I wasstudied with electrophoretic techniques and it was proved that ligands 4 and 5 inhibited this enzymeat a concentration of 30 M. The biological activityof the novel compounds was assessed through anexamination of changes in cell cycle distribution, mitochondrial membrane potential and cellular via-bility. Inhibitors 3-5 exhibited a cytotoxic effect on HL-60 (human acute promyelocytic leu

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    FR - Pharmacology and apothecary chemistry

  • 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

    International Journal of Biological Macromolecules

  • ISSN

    0141-8130

  • e-ISSN

  • Volume of the periodical

    64

  • Issue of the periodical within the volume

    March

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    10

  • Pages from-to

    53-62

  • UT code for WoS article

    000334147300009

  • EID of the result in the Scopus database