2022
DOI: 10.1590/s2175-97902020000118747
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New and potential properties, characteristics, and analytical methods of ferulic acid: A review

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Cited by 16 publications
(7 citation statements)
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“…From the eight phenolic compounds found in our phenolic fraction of the P. arabica extract, the highest component concentration was ferulic acid (3.992 mg/gm) with a retention time of 3.22 min, which may contribute to the high efficacy of the phenolic extract as a cytotoxic biological chemical on different cancer cell lines. 29 Research has indicated that ferulic acid induces cell death by decreasing the Bcl-2 and increasing the BAX gene expression or by upregulation of caspase-3 and cleaved caspase-9. 30 The highest component of the terpene fraction was campesterol (4.358 mg/gm), with a retention time of 11.5 min.…”
Section: Discussionmentioning
confidence: 99%
“…From the eight phenolic compounds found in our phenolic fraction of the P. arabica extract, the highest component concentration was ferulic acid (3.992 mg/gm) with a retention time of 3.22 min, which may contribute to the high efficacy of the phenolic extract as a cytotoxic biological chemical on different cancer cell lines. 29 Research has indicated that ferulic acid induces cell death by decreasing the Bcl-2 and increasing the BAX gene expression or by upregulation of caspase-3 and cleaved caspase-9. 30 The highest component of the terpene fraction was campesterol (4.358 mg/gm), with a retention time of 11.5 min.…”
Section: Discussionmentioning
confidence: 99%
“…In addition, high levels of FA were found in the shoot after HVED treatment. Marcato et al [ 76 ] observed that FA can absorb UV radiation through the creation of phenoxy radicals, resulting in cis-trans isomerization. Based on this, it is possible that FA might have a role in UV protection.…”
Section: Discussionmentioning
confidence: 99%
“…Furthermore, ferulic acid can be obtained by organic synthesis to improve yield and reduce preparation times. One method of ferulic acid synthesis is the condensation reaction of Knoevenagel-Doebner vanillin with malonic acid using piperidine [18] or proline [19] as a catalyst and microwave-assisted reaction [19][20][21] Ferulic acid has a relative molecular weight of 194 g/mol, a melting point of 174 o C, poor stability in an aqueous solution, and is soluble in hot water, methanol, ethanol, and acetone [22]. Ferulic acid is relatively hydrophilic, with an apparent partition coefficient of 0.3753 at pH 3 and 0.489 at pH 10.…”
Section: Refmentioning
confidence: 99%
“…Combining the phenolic ring and unsaturated side chain causes a resonance-stabilized phenoxy radical. The resonance stabilization explains how ferulic acid has an effective antioxidant capacity [22]. It might provide more sites for free radicals to attack and prevent them from destroying the cell membrane [27].…”
Section: Refmentioning
confidence: 99%