1996
DOI: 10.1016/0891-5849(95)02014-4
|View full text |Cite
|
Sign up to set email alerts
|

Antioxidant properties of hydroxy-flavones

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

11
260
1
6

Year Published

1998
1998
2020
2020

Publication Types

Select...
6
2

Relationship

0
8

Authors

Journals

citations
Cited by 624 publications
(278 citation statements)
references
References 12 publications
11
260
1
6
Order By: Relevance
“…Another important matter is that ABTS + can be dissolved in aqueous and organic media, in which the antioxidant activity can be measured, due to the hydrophilic and lipophilic nature of the compounds, those existed in the plant cells. In contrast, DPPH has been used extensively as a free radical to evaluate reducing substances (Cotelle et al 1996) and is a useful reagent for investigating the free radical scavenging activities of polyphenol compounds (Duan et al 2006). Many researchers have reported positive correlation between free radical scavenging activity.…”
Section: Introductionmentioning
confidence: 99%
“…Another important matter is that ABTS + can be dissolved in aqueous and organic media, in which the antioxidant activity can be measured, due to the hydrophilic and lipophilic nature of the compounds, those existed in the plant cells. In contrast, DPPH has been used extensively as a free radical to evaluate reducing substances (Cotelle et al 1996) and is a useful reagent for investigating the free radical scavenging activities of polyphenol compounds (Duan et al 2006). Many researchers have reported positive correlation between free radical scavenging activity.…”
Section: Introductionmentioning
confidence: 99%
“…It's known that antiradical activity of phenolic compounds depends on their molecular structure which is related to availability of phenolic hydrogens and the possibility of stabilization of the resulting phenoxyl radicals formed by hydrogen donation (Pannala et al, 2001). Ferulic acid, due to its phenolic nucleus and an extended side chain conjugation, quickly forms a resonance stabilized phenox radical which accounts for its potent antioxidant potencial, but ferulic acid can not form a metal chelate (Cotelle et al, 1996). The esterification of the carboxyl group seems to affect the antiradical activity of phenolic acids in a different way.…”
Section: Phytochemistry Of Ananas Bracteatusmentioning
confidence: 99%
“…The authors suggest that when the carboxyl group of coplanar conformation compounds was esterified, the rotation of the phenyl moiety may have been restrained, leading to conformational modification that enhances antiradical activity. Ferulic acid derivatives are expected to be more effective than p-coumaric acid derivates because the electron-donating methoxy group allows increased stabilization of the resulting aryloxyl radical through electron delocalization after hydrogen donation by the hydroxyl group (Cotelle et al, 1996).…”
Section: Phytochemistry Of Ananas Bracteatusmentioning
confidence: 99%
See 1 more Smart Citation
“…The antioxidant capacity (AC) or activity of the extract was measured by DPPH + (2,2-diphenyl-1-picrylhydrazyl), according to the method of Cottele et al (1996). Results were expressed in µg of ascorbic acid equivalent per mL (AAE µg/mL).…”
Section: Determination Of Antioxidant Capacitymentioning
confidence: 99%