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Enhanced Absorption and Growth Inhibition with Amino Acid Monoester Prodrugs of Floxuridine by Targeting hPEPT1 Transporters

A series of amino acid monoester prodrugs of floxuridine was synthesized and evaluated for the improvement of oral bioavailability and the feasibility of target drug delivery via oligopeptide transporters. All floxuridine 5′-amino acid monoester prodrugs exhibited PEPT1 affinity, with inhibition coe...

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Bibliografski detalji
Izdano u:Molecules
Glavni autori: Tsume, Yasuhiro, Vig, Balvinder S., Sun, Jing, Landowski, Christopher P., Hilfinger, John M., Ramachandran, Chandrasekharan, Amidon, Gordon L
Format: Artigo
Jezik:Inglês
Izdano: MDPI 2008
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6244841/
https://ncbi.nlm.nih.gov/pubmed/18719516
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/molecules13071441
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