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Fluorinated derivatives of 2-phenyl-3-hydroxy-4(1H)-quinolinone as tubulin polymerization inhibitors

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15110%2F20%3A73601222" target="_blank" >RIV/61989592:15110/20:73601222 - isvavai.cz</a>

  • Alternative codes found

    RIV/61989592:15310/20:73601222

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S0223523420301434?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0223523420301434?via%3Dihub</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.ejmech.2020.112176" target="_blank" >10.1016/j.ejmech.2020.112176</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Fluorinated derivatives of 2-phenyl-3-hydroxy-4(1H)-quinolinone as tubulin polymerization inhibitors

  • Original language description

    The previous studies of the derivatives of 2-phenyl-3-hydroxy-4(1H)-quinolinone (3-HQs) recognized these compounds to exhibit anticancer activity in vitro in the native state [[1], [2], [3], [4], [5], [6], [7]] or as mixed-ligand complexes with various metals [[8], [9], [10], [11], [12]]. Although these studies described the number of derivatives to have exciting anticancer activity, only two papers revealed a possible molecular target. In the first study, Sui et al. [13] reported the inhibition of topoisomerase as an expected molecular target. The authors found some derivatives with higher activity against mammalian topoisomerase than ellipticine. Recently published interaction of other 3-HQs derivatives with elongation factor eEF1A1 inside the cancer cells revealed another possible mechanism of anticancer activity [14].

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10608 - Biochemistry and molecular biology

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2020

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

  • ISSN

    0223-5234

  • e-ISSN

  • Volume of the periodical

    192

  • Issue of the periodical within the volume

    April 15 2020

  • Country of publishing house

    FR - FRANCE

  • Number of pages

    9

  • Pages from-to

    "'nestránkováno'"

  • UT code for WoS article

    000523563100017

  • EID of the result in the Scopus database

    2-s2.0-85080081774