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- W2892564394 endingPage "371" @default.
- W2892564394 startingPage "361" @default.
- W2892564394 abstract "Quercetin is the main flavonoid in the diet. Found in large amounts in capers, red onion, wine, and apple's skin as glycoside, it is rapidly transformed into the corresponding aglycone after digestion. Although it has numerous healthy and therapeutic properties, quercetin finds few applications due to its low bioavailability. Among the five-hydroxyl groups, 3-OH seems to be the most susceptible to autoxidation, in addition to the 2,3-double bond. Furthermore, the C3′–C4′ positions are the most glucuronidated. Therefore, to be able to use quercetin as a nutraceutical or drug, it is mandatory to optimize its chemical structure. A chemical modification overcoming this phenomenon is the esterification. The ester derivatives of quercetin secure the structure during storage/use and after its systemic introduction, improving the shelf life. In this chapter the metabolic limit of quercetin use is outlined by a concise description of its metabolic fate and some chemical modifications performed to ameliorate the therapeutic profile." @default.
- W2892564394 created "2018-10-05" @default.
- W2892564394 creator A5009428493 @default.
- W2892564394 creator A5081901402 @default.
- W2892564394 creator A5082275152 @default.
- W2892564394 date "2018-01-01" @default.
- W2892564394 modified "2023-10-14" @default.
- W2892564394 title "Bioavailability and Biochemistry of Quercetin and Applications to Health and Diseases" @default.
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