2013
DOI: 10.1002/chin.201329266
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ChemInform Abstract: Biological Properties of Hydroxytyrosol and Its Derivatives

Abstract: Review: 93 refs.

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Cited by 6 publications
(9 citation statements)
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“…31 Thus, HT and its derivatives inhibit chain propagation by donating a hydrogen to the alkylperoxyl radicals formed in the initiation step, and the resulting phenoxy radical is stabilized by an intramolecular Hbond with the −OH group. 32 The application of the pseudophase kinetic model to determining AO distributions and interfacial AO concentrations has already been published elsewhere and is briefly described in the Supporting Information (section S1). The results obtained here with HT and its esters confirm the relationships between the AO efficiency and the percentage of AO in the interfacial region previously demonstrated for the gallic 11 and caffeic 10 acid ester series.…”
Section: ■ Introductionsupporting
confidence: 89%
“…31 Thus, HT and its derivatives inhibit chain propagation by donating a hydrogen to the alkylperoxyl radicals formed in the initiation step, and the resulting phenoxy radical is stabilized by an intramolecular Hbond with the −OH group. 32 The application of the pseudophase kinetic model to determining AO distributions and interfacial AO concentrations has already been published elsewhere and is briefly described in the Supporting Information (section S1). The results obtained here with HT and its esters confirm the relationships between the AO efficiency and the percentage of AO in the interfacial region previously demonstrated for the gallic 11 and caffeic 10 acid ester series.…”
Section: ■ Introductionsupporting
confidence: 89%
“…The results were reported as mg AAE/g. The methodology outlined by Patel [65] and Ali et al [62] was slightly modified in order to determine the ferrous ion chelating activity using 562nm absorbance. Using this approach, 15μL of extract was combined with 50μL of ferrous chloride (2 mM), 85μL of water and 50μL of ferrozine (5mM), as well as the mixture was incubated at 25°C for 10 minutes.…”
Section: Antioxidant Potentialmentioning
confidence: 99%
“…In the past few years, a large number of HTyr-derived compounds have been synthesized, and several of them have been described in recent reviews. In particular, many experiments have been performed to synthesize HTyr derivatives and analogues with a better hydrophilic/lipophilic balance (HLB) to increase their availability and to join HTyr to other biologically active compounds to enhance its biological functions. The biological activities of HTyr-derived compounds have been evaluated in cell-free and cell-based models, and, as reported by Manna et al, the results obtained from the use of the two different experimental models were not always comparable.…”
Section: Introductionmentioning
confidence: 99%