2018
DOI: 10.31788/rjc.2018.1143051
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Synthesis and Antioxidant Activity of Prenylated Resveratrol

Abstract: Resveratrol derivatives have been reported to have important bioactivities. Synthesis of monomeric resveratrol derivatives has been a challenging topic in both organic and medicinal chemistry. A Synthesis of prenylated resveratrol was developed through prenylation between resveratrol (3,5,4'-trihydroxystilbene) and prenyl bromide (3,3-dimethyl allyl bromide) using heterogeneous superbase catalyst γ-Al2O3/NaOH/Na. The aim of this research is to obtain prenylated resveratrol compound that has important bioactivi… Show more

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Cited by 3 publications
(2 citation statements)
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“…The antioxidant activities of synthesized compounds (2a-e) and vanillic acid evaluated spectrophotometrically following the procedure of free-radical DPPH scavenger and Ferric ion Reducing Activity Potential (FRAP) as reported previously, with slight modification. 5,[17][18] Quercetin was used as a standard.…”
Section: In Vitro Antioxidant Assaymentioning
confidence: 99%
“…The antioxidant activities of synthesized compounds (2a-e) and vanillic acid evaluated spectrophotometrically following the procedure of free-radical DPPH scavenger and Ferric ion Reducing Activity Potential (FRAP) as reported previously, with slight modification. 5,[17][18] Quercetin was used as a standard.…”
Section: In Vitro Antioxidant Assaymentioning
confidence: 99%
“…Polyphenols are commonly divided into flavonoids and the hydroxyl cinnamic acids [3][4][5] . Vanillic acid is a naturally occurring active compound having antimicrobial, anti-inflammatory and antioxidant / anticancer properties, we thought of synthesizing compounds with a novel ether, ester and hybrid derivatives of vanillic acid wherein vanillic acid would be etherified, esterified and hybridized with various other compounds and to check whether these compounds possess above biological activities [6][7][8][9][10][11][12][13][14][15][16][17][18] . The objective of this study is to condense two molecules of the same disease domain to produce more potent candidate in the same disease domain or to condense two molecules of different disease domain to produce a mixed variety of those disease domain or to have drug candidate with entirely different biological activity.…”
Section: Introductionmentioning
confidence: 99%