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- W2078128477 abstract "A major hurdle impeding the successful clinical development of drug candidates can be poor intestinal permeability. Low intestinal permeability may be enhanced by a prodrug approach targeting membrane transporters in the small intestine. Transporter specificity, affinity, and capacity are three factors in targeted prodrug design. The human apical sodium dependent bile acid transporter (SLC10A2) belongs to the solute carrier family (SLC) of transporters and is an important carrier protein expressed in the small intestine. In spite of its appearing to be an excellent target for prodrug design, few studies have targeted human apical sodium dependent bile acid transporter (hASBT) to improve oral bioavailability. This review discusses bile acids including their chemistry and their absorptive disposition. Additionally, hASBT-mediated prodrug targeting is discussed, including QSAR, in vitro models for hASBT assay, and the current progress in utilizing hASBT as a drug delivery target." @default.
- W2078128477 created "2016-06-24" @default.
- W2078128477 creator A5044356220 @default.
- W2078128477 creator A5073615016 @default.
- W2078128477 date "2006-05-11" @default.
- W2078128477 modified "2023-10-14" @default.
- W2078128477 title "Apical Sodium Dependent Bile Acid Transporter (ASBT, SLC10A2): A Potential Prodrug Target" @default.
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- W2078128477 doi "https://doi.org/10.1021/mp060022d" @default.
- W2078128477 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2796132" @default.
- W2078128477 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/16749855" @default.
- W2078128477 hasPublicationYear "2006" @default.
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