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- W2029142438 abstract "Three half-ester derivatives 10-12 of 5'-O-2',3'-dideoxydidanosine (DDI, 1) have been synthesized. The compounds exhibited excellent correlation between partition coefficients LogP and relative in vitro bovine serum albumin binding. Using high-performance liquid chromatography-mass spectrometry (LC-MS), DDI (1) was quantitatively determined in rat plasma after intravenous injection of the azelaic acid monoester derivative (11) of DDI. The pharmacokinetic data obtained for DDI were consistent with literature. The pharmacokinetic profile of 11 showed no significant difference in AUC(0-360) or curve shape compared to the parent drug DDI (1). The data indicate that the prodrug was converted to DDI within minutes after administration. High relative protein binding in vitro holds a promise for validity of the concept using more stable linker bonds." @default.
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- W2029142438 date "2009-10-01" @default.
- W2029142438 modified "2023-09-28" @default.
- W2029142438 title "Didanosine ester prodrugs: Synthesis, albumin binding properties and pharmacokinetic studies in rats" @default.
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- W2029142438 doi "https://doi.org/10.1016/j.ejmech.2009.04.008" @default.
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