Electrochemical behavior and antioxidant and prooxidant activity of natural phenolics.Molecules. 2007 Oct 24; 12(10):2327-40.M
Abstract
We have investigated the electrochemical oxidation of a number natural phenolics (salicylic acid, m-hydroxybenzoic acid, p-hydroxybenzoic acid, protocatechuic acid, o-coumaric acid, m-coumaric acid, p-coumaric acid, caffeic acid, quercetin and rutin) using cyclic voltammetry. The antioxidant properties of these compounds were also studied. A structural analysis of the tested phenolics suggests that multiple OH substitution and conjugation are important determinants of the free radical scavenging activity and electrochemical behavior. Compounds with low oxidation potentials (Epa lower than 0.45) showed antioxidant activity, whereas compounds with high Epa values (>0.45) act as prooxidants.
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MeSH
Pub Type(s)
Journal Article
Language
eng
PubMed ID
17978760
Citation
Simić, Aleksandra, et al. "Electrochemical Behavior and Antioxidant and Prooxidant Activity of Natural Phenolics." Molecules (Basel, Switzerland), vol. 12, no. 10, 2007, pp. 2327-40.
Simić A, Manojlović D, Segan D, et al. Electrochemical behavior and antioxidant and prooxidant activity of natural phenolics. Molecules. 2007;12(10):2327-40.
Simić, A., Manojlović, D., Segan, D., & Todorović, M. (2007). Electrochemical behavior and antioxidant and prooxidant activity of natural phenolics. Molecules (Basel, Switzerland), 12(10), 2327-40.
Simić A, et al. Electrochemical Behavior and Antioxidant and Prooxidant Activity of Natural Phenolics. Molecules. 2007 Oct 24;12(10):2327-40. PubMed PMID: 17978760.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Electrochemical behavior and antioxidant and prooxidant activity of natural phenolics.
AU - Simić,Aleksandra,
AU - Manojlović,Dragan,
AU - Segan,Dejan,
AU - Todorović,Marija,
Y1 - 2007/10/24/
PY - 2007/06/15/received
PY - 2007/10/04/revised
PY - 2007/10/04/accepted
PY - 2007/11/6/pubmed
PY - 2007/12/19/medline
PY - 2007/11/6/entrez
SP - 2327
EP - 40
JF - Molecules (Basel, Switzerland)
JO - Molecules
VL - 12
IS - 10
N2 - We have investigated the electrochemical oxidation of a number natural phenolics (salicylic acid, m-hydroxybenzoic acid, p-hydroxybenzoic acid, protocatechuic acid, o-coumaric acid, m-coumaric acid, p-coumaric acid, caffeic acid, quercetin and rutin) using cyclic voltammetry. The antioxidant properties of these compounds were also studied. A structural analysis of the tested phenolics suggests that multiple OH substitution and conjugation are important determinants of the free radical scavenging activity and electrochemical behavior. Compounds with low oxidation potentials (Epa lower than 0.45) showed antioxidant activity, whereas compounds with high Epa values (>0.45) act as prooxidants.
SN - 1420-3049
UR - https://www.unboundmedicine.com/medline/citation/17978760/Electrochemical_behavior_and_antioxidant_and_prooxidant_activity_of_natural_phenolics_
L2 - https://www.mdpi.com/resolver?pii=12102327
DB - PRIME
DP - Unbound Medicine
ER -