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Purin-6-one and pyrrolo[2,3-d]pyrimidin-4-one derivatives as potentiating agents of doxorubicin cytotoxicity

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60162694%3AG44__%2F18%3A43889573" target="_blank" >RIV/60162694:G44__/18:43889573 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11150/18:10379320 RIV/00216208:11160/18:10379320 RIV/00179906:_____/18:10379320

  • Result on the web

    <a href="https://www.future-science.com/doi/pdf/10.4155/fmc-2018-0086" target="_blank" >https://www.future-science.com/doi/pdf/10.4155/fmc-2018-0086</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.4155/fmc-2018-0086" target="_blank" >10.4155/fmc-2018-0086</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Purin-6-one and pyrrolo[2,3-d]pyrimidin-4-one derivatives as potentiating agents of doxorubicin cytotoxicity

  • Original language description

    Aim: DNA damage response plays an eminent role in patients&apos; response to conventional chemotherapy and radiotherapy. Its inhibition is of great interest as it can overcome cancer cell resistance and reduce the effective doses of DNA damaging agents. Results &amp; methodology: We have focused our research on phos-phatidylinositol 3-kinase-related kinases and prepared 35 novel compounds through a scaffold hopping approach. The newly synthesized inhibitors were tested on a panel of nine cancer and one healthy cell lines alone and in combination with appropriate doses of doxorubicin. Conclusion: Five novel compounds 4f, 10b, 15g, 7e and 15f in combination with doxorubicin showed significant antiproliferative effect on seven cancer cell lines while not affecting the cell growth alone.

  • 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

    30107 - Medicinal chemistry

Result continuities

  • Project

    <a href="/en/project/TG02010020" target="_blank" >TG02010020: Centre for Transfer of Biomedical Technologies - PoC</a><br>

  • Continuities

    S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2018

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Future Medicinal Chemistry

  • ISSN

    1756-8919

  • e-ISSN

  • Volume of the periodical

    10

  • Issue of the periodical within the volume

    17

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    10

  • Pages from-to

    2029-2038

  • UT code for WoS article

    000443173800003

  • EID of the result in the Scopus database

    2-s2.0-85052708059