Dried Fruits 2013
DOI: 10.1002/9781118464663.ch12
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Phytochemicals and Health Benefits of Dried Apricots

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Cited by 5 publications
(4 citation statements)
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“…The enzymatic oxidation is followed by non-enzymatic polymerization of the resulted quinones into dark/brown polymers called melanins [43]. Apricot PPO remains active at drying temperature below 55 °C [44], and since TSD was performed at temperatures ~ 40 ° C, enzymatic browning is mostly the main cause of phenolic compounds decrease in TSD apricots. This was also visually confirmed, where the dried apricots had dark colors.…”
Section: Discussionmentioning
confidence: 99%
“…The enzymatic oxidation is followed by non-enzymatic polymerization of the resulted quinones into dark/brown polymers called melanins [43]. Apricot PPO remains active at drying temperature below 55 °C [44], and since TSD was performed at temperatures ~ 40 ° C, enzymatic browning is mostly the main cause of phenolic compounds decrease in TSD apricots. This was also visually confirmed, where the dried apricots had dark colors.…”
Section: Discussionmentioning
confidence: 99%
“…Studies [30,34,35] continue to support the beneficial effects of TDF specifically in traditional fruit juice beverages in enhancing perceived satiety, regulating energy intake, modulating gastric emptying, and reducing weight gain. Previous studies [36][37][38][39][40][41][42] have also supported the potential activity of some traditional Egyptian beverages as functional foods with antioxidative, antihypertensive, hypolipidemic, and anti-carcinogenic properties particularly in hibiscus tea, tamarind juice, dried apricot juice, and carob juice. In addition, the potential benefits of guava, strawberries, and pomegranate for the prevention of obesity and obesity-related diseases have been previously demonstrated [43][44][45][46][47][48].…”
Section: Discussionmentioning
confidence: 76%
“…Classical medicinal approaches rely on orthosteric and allosteric inhibitors for direct target inhibition. Approaches such as (a) preferential protein subtype selectivity [180,181], or species-specific selectivity [182,183], (b) cyclization or rigidification in inhibitor design [184][185][186][187][188][189], (c) targeting heterodimeric proteins or receptors [12,190,191]), (d) identification of toxicophore to pharmacophore [192][193][194][195], (e) repurposing of drugs of clinical agents [196], (f) inverse screening [197,198]), and (g) exploration of natural phytochemicals [199][200][201] have gained interest in the recent decade. As these approaches focus on small molecule inhibitors (SMIs) and their related modes of action; therefore, often have issues that are typical with occupancy-driven pharmacology (shown in Figure 1A), such as (a) frequent occurrence of resistance after prolonged use and, (b) require a higher degree of potency to achieve full inhibition of protein of interest (POI).…”
Section: Discussionmentioning
confidence: 99%