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Interactions with selected drug renal transporters and transporter-mediated cytotoxicity in antiviral agents from the group of acyclic nucleoside phosphonates

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F13%3A00397563" target="_blank" >RIV/61388963:_____/13:00397563 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11160/13:10144051

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.tox.2013.07.004" target="_blank" >http://dx.doi.org/10.1016/j.tox.2013.07.004</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.tox.2013.07.004" target="_blank" >10.1016/j.tox.2013.07.004</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Interactions with selected drug renal transporters and transporter-mediated cytotoxicity in antiviral agents from the group of acyclic nucleoside phosphonates

  • Original language description

    Acyclic nucleoside phosphonates (ANPs) possess antiviral and antiproliferative activities. This study investigated in vitro relationships between the affinity of several structurally related potent ANPs to selected human transporters and their cytotoxicity. SLC (solute carrier family) transporters (hOAT1, hOCT2, hCNT2, hCNT3) and ABC (ATP-binding cassette) transporters (MDR1, BCRP), which are typically expressed in the kidney, were included in the study. Most of the ANPs studied showed the potency to interact with hOAT1 and GS-9191, a double prodrug of PMEG, displayed an affinity for hOAT1 comparable with that of adefovir and tenofovir. The study documented that among the studied transporters hOAT1 seems to be the decisive determinant for renal handling in most of the tested ANPs. This transporter may also play an important role in the mechanism of their potential cytotoxic effects.

  • 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

    <a href="/en/project/NT12398" target="_blank" >NT12398: Study on relationships between toxicity and transport mechanism of antivirals</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

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

    Toxicology

  • ISSN

    0300-483X

  • e-ISSN

  • Volume of the periodical

    311

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    IE - IRELAND

  • Number of pages

    12

  • Pages from-to

    135-146

  • UT code for WoS article

    000324609200006

  • EID of the result in the Scopus database