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Synthesis and Antioxidant Activity of Alkyl Nitroderivatives of Hydroxytyrosol

 

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Opened Access Synthesis and Antioxidant Activity of Alkyl Nitroderivatives of Hydroxytyrosol
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Author: Gallardo Morillo, Elena
Palma Valdés, Rocío
Sarriá, Beatriz
Gallardo, Irene
Cruz, José P. de la
Bravo, Laura
Mateos, Raquel
Espartero Sánchez, José Luis
Department: Universidad de Sevilla. Departamento de Bioquímica y Biología Molecular
Date: 2016
Published in: Molecules, 21 (5), 656-.
Document type: Article
Abstract: A series of alkyl nitrohydroxytyrosyl ether derivatives has been synthesized from free hydroxytyrosol (HT), the natural olive oil phenol, in order to increase the assortment of compounds with potential neuroprotective activity in Parkinson’s disease. In this work, the antioxidant activity of these novel compounds has been evaluated using Ferric Reducing Antioxidant Power (FRAP), 2,2′-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS), and Oxygen Radical Scavenging Capacity (ORAC) assays compared to that of nitrohydroxytyrosol (NO2HT) and free HT. New compounds showed variable antioxidant activity depending on the alkyl side chain length; compounds with short chains (2–4 carbon atoms) maintained or even improved the antioxidant activity compared to NO2HT and/or HT, whereas those with longer side chains (6–8 carbon atoms) showed lower activity than NO2HT but higher than HT.
Cite: Gallardo Morillo, E., Palma Valdés, R., Sarriá, B., Gallardo, I., Cruz, J.P.d.l., Bravo, L.,...,Espartero Sánchez, J.L. (2016). Synthesis and Antioxidant Activity of Alkyl Nitroderivatives of Hydroxytyrosol. Molecules, 21 (5), 656-.
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URI: http://hdl.handle.net/11441/47098

DOI: http://dx.doi.org/10.3390/molecules21050656

This work is under a Creative Commons License: 
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