Academic Journal

Synthesis and Antioxidant Activity of Alkyl Nitroderivatives of Hydroxytyrosol.

التفاصيل البيبلوغرافية
العنوان: Synthesis and Antioxidant Activity of Alkyl Nitroderivatives of Hydroxytyrosol.
المؤلفون: Gallardo, Elena, Palma-Valdés, Rocío, Sarriá, Beatriz, Gallardo, Irene, de la Cruz, José P, Bravo, Laura, Mateos, Raquel, Espartero, José L
سنة النشر: 2016
المجموعة: Sistema Sanitario Público de Andalucía (SSPA): Repositorio
مصطلحات موضوعية: Parkinson’s disease, alkyl nitrohydroxytyrosyl derivatives, antioxidant activity, hydroxytyrosol, nitrocatechol, Antioxidants, Benzothiazoles, Carbon, Fluorescence Recovery After Photobleaching, Free Radical Scavengers, Humans, Nitrogen Dioxide, Oxidation-Reduction, Oxygen, Phenol, Phenols, Phenylethyl Alcohol, Reactive Oxygen Species, Sesame Oil, Sulfonic Acids
الوصف: 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.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
تدمد: 1420-3049
Relation: http://hdl.handle.net/10668/10117; PMC6272824; https://www.mdpi.com/1420-3049/21/5/656/pdf?version=1463570852; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272824/pdf
DOI: 10.3390/molecules21050656
الاتاحة: http://hdl.handle.net/10668/10117
https://doi.org/10.3390/molecules21050656
https://www.mdpi.com/1420-3049/21/5/656/pdf?version=1463570852
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272824/pdf
Rights: Attribution 4.0 International ; http://creativecommons.org/licenses/by/4.0/ ; open access
رقم الانضمام: edsbas.4AD210E7
قاعدة البيانات: BASE
الوصف
تدمد:14203049
DOI:10.3390/molecules21050656