2020
DOI: 10.1016/j.molstruc.2020.128749
|View full text |Cite
|
Sign up to set email alerts
|

Syringic and cinnamic acids antiradical/antioxidant activities as R. ferruginea extract components and membrane physico-chemical influence

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2021
2021
2024
2024

Publication Types

Select...
5
2

Relationship

0
7

Authors

Journals

citations
Cited by 8 publications
(2 citation statements)
references
References 52 publications
0
2
0
Order By: Relevance
“…Cinnamic acid derivatives may also be very potent antioxidants due to their ability to act via the HAT mechanism, forming a stable phenoxyl radical [48,49]. The high-DPPH activity of the liquor may have resulted from the presence of cinnamic acid, as the content of this compound was significantly higher that in the brandy (Table 3).…”
Section: Resultsmentioning
confidence: 99%
“…Cinnamic acid derivatives may also be very potent antioxidants due to their ability to act via the HAT mechanism, forming a stable phenoxyl radical [48,49]. The high-DPPH activity of the liquor may have resulted from the presence of cinnamic acid, as the content of this compound was significantly higher that in the brandy (Table 3).…”
Section: Resultsmentioning
confidence: 99%
“…Although there are few studies that evaluate the antioxidant potential in vitro of extracts from this species, there are studies where the majority of its SMs have been determined in DPPH inhibition as syringic acid (IC 50 = 1.5 µg/mL, [25]), vanillic acid (20 µm inhibits almost 30%, [26]), ferulic acid (IC 50 = 1 µm, [27]), phlorizin (IC 50 = 10 mM, [28]), phloretin (IC 50 = 0.6 mmol/L, [29]) and α-amyrin (IC 50 = 10 mM, [30]). Hence, the notorious value of IC 50 shown by the MECP on the radical DPPH is due to the majority presence of these SMs identified in MECP using the HPLC technique.…”
Section: Discussionmentioning
confidence: 99%