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Title: Antioxidant properties of 3-hydroxycoumarin derivatives. Author: Bailly F, Maurin C, Teissier E, Vezin H, Cotelle P. Journal: Bioorg Med Chem; 2004 Nov 01; 12(21):5611-8. PubMed ID: 15465339. Abstract: A series of hydroxylated 3-hydroxycoumarins was synthesised by the reaction of 3-aryl-2-hydroxypropenoic derivatives with boron tribromide. They were evaluated for their ability to scavenge the 2,2-diphenyl-1-picrylhydrazyl radical, the superoxide anion radical, the hydroxyl radical and the peroxynitrite anion and to inhibit copper-induced human LDL peroxidation. The physicochemical results were in accordance to establish the compounds hydroxylated on C-6 and C-7 positions as the most active of the series with antioxidant potencies comparable to those of quercetin and vitamin C. These compounds form o- and p-quinonoid derivatives upon radical scavenging and may serve as new lead compounds for pharmacological investigations.[Abstract] [Full Text] [Related] [New Search]