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- W2023908498 endingPage "15917" @default.
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- W2023908498 abstract "Low bioavailability severely hinders exploitation of the biomedical potential of resveratrol. Extensive phase-II metabolism and poor water solubility contribute to lowering the concentrations of resveratrol in the bloodstream after oral administration. Prodrugs may provide a solution-protection of the phenolic functions hinders conjugative metabolism and can be exploited to modulate the physicochemical properties of the compound. We report here the synthesis and characterization of carbamate ester derivatives of resveratrol bearing on each nitrogen atom a methyl group and either a methoxy-poly(ethylene glycol)-350 (mPEG-350) or a butyl-glucosyl promoiety conferring high water solubility. Ex vivo absorption studies revealed that the butyl-glucosyl conjugate, unlike the mPEG-350 one, is able to permeate the intestinal wall. In vivo pharmacokinetics confirmed absorption after oral administration and showed that no hydrolysis of the carbamate groups takes place. Thus, sugar groups can be attached to resveratrol to obtain soluble derivatives maintaining to some degree the ability to permeate biomembranes, perhaps by facilitated or active transport." @default.
- W2023908498 created "2016-06-24" @default.
- W2023908498 creator A5001169698 @default.
- W2023908498 creator A5026035111 @default.
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- W2023908498 creator A5053578537 @default.
- W2023908498 creator A5065244580 @default.
- W2023908498 creator A5081232383 @default.
- W2023908498 date "2014-10-01" @default.
- W2023908498 modified "2023-10-14" @default.
- W2023908498 title "New Water-Soluble Carbamate Ester Derivatives of Resveratrol" @default.
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