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
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Czech description
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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
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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
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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
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