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LC/MS metabolic study on quercetin and taxifolin galloyl esters using human hepatocytes as toxicity and biotransformation in vitro cell model

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F13%3A33144017" target="_blank" >RIV/61989592:15310/13:33144017 - isvavai.cz</a>

  • Alternative codes found

    RIV/61388971:_____/13:00424179 RIV/61989592:15110/13:33144017

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.jpba.2013.07.045" target="_blank" >http://dx.doi.org/10.1016/j.jpba.2013.07.045</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jpba.2013.07.045" target="_blank" >10.1016/j.jpba.2013.07.045</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    LC/MS metabolic study on quercetin and taxifolin galloyl esters using human hepatocytes as toxicity and biotransformation in vitro cell model

  • Original language description

    Galloyl esters of quercetin and taxifolin have been recently prepared semisynthetically as part of work towards modifying the solubility and modulating the biological aktivity of these natural flavonoids. In this paper we focused on the liquid chromatography?mass spektrometry (LC?MS) profiling of metabolites of 3-O-galloylquercetin and 7-O-galloyltaxifolin using human hepatocytes as the in vitro cell model. A subtoxic concentration (50 M) was used for both compounds and the formation of metabolites wasmonitored for 2 h in hepatocytes and cultivation medium separately. Using negative electrospray ionization-quadrupole time-of-flight mass spektrometry (ESI-QqTOF MS), we identified different biotransformation patterns for the studied compounds. 3-O-Galloylquercetin is metabolized directly to glucuronides and methyl derivatives. In contrast, 7-O-galloyltaxifolin is oxidized to 7-O-galloylquercetin or cleaved to taxifolin, and consequently the products formed are sulfated or glucuronidated

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    CE - Biochemistry

  • OECD FORD branch

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

    2013

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Journal of Pharmaceutical and Biomedical Analysis

  • ISSN

    0731-7085

  • e-ISSN

  • Volume of the periodical

    86

  • Issue of the periodical within the volume

    DEC

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    8

  • Pages from-to

    135-142

  • UT code for WoS article

  • EID of the result in the Scopus database