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Synergy between azoles and 1,4-dihydropyridine derivative as an option to control fungal infections

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F17%3A10370616" target="_blank" >RIV/00216208:11320/17:10370616 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1007/s10482-017-0895-6" target="_blank" >http://dx.doi.org/10.1007/s10482-017-0895-6</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s10482-017-0895-6" target="_blank" >10.1007/s10482-017-0895-6</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Synergy between azoles and 1,4-dihydropyridine derivative as an option to control fungal infections

  • Original language description

    With emerging fungal infections and developing resistance, there is a need for understanding the mechanisms of resistance as well as its clinical impact while planning the treatment strategies. Several approaches could be taken to overcome the problems arising from the management of fungal diseases. Besides the discovery of novel effective agents, one realistic alternative is to enhance the activity of existing agents. This strategy could be achieved by combining existing antifungal agents with other bioactive substances with known activity profiles (combination therapy). Azole antifungals are the most frequently used class of substances used to treat fungal infections. Fluconazole is often the first choice for antifungal treatment. The aim of this work was to study potential synergy between azoles and 1,4-dihydropyridine-2,3,5-tricarboxylate (termed derivative H) in order to control fungal infections. This article points out the synergy between azoles and newly synthesized derivative H in order to fight fungal infections. Experiments confirmed the role of derivative H as substrate/inhibitor of fungal transporter Cdr1p relating to increased sensitivity to fluconazole. These findings, plus decreased expression of ERG11, are responsible for the synergistic effect.

  • 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

    10610 - Biophysics

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2017

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Antonie van Leeuwenhoek

  • ISSN

    0003-6072

  • e-ISSN

  • Volume of the periodical

    110

  • Issue of the periodical within the volume

    9

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    8

  • Pages from-to

    1219-1226

  • UT code for WoS article

    000407842000011

  • EID of the result in the Scopus database

    2-s2.0-85020238120