Journal of Enzyme Inhibition and Medicinal Chemistry · 2007 · 98 citations · 68 references
AgriculturePharmacologyBioisosterismFood ChemistryStructure-activity RelationshipsAntioxidant DefensePhenolic Compound AnalysisAntioxidant Activity AssaysAntioxidant Capacity AssaysAntioxidant PropertiesFree Radical ScavengingNatural AntioxidantsPhenolic Compound Antioxidant CapacityScavengingSynthetic Antioxidants
In this study, di(2,6-dimethylphenol) (Di-DMP), di(2,6-diisopropylphenol) (Di-DIP, dipropofol) and di(2,6-di-t-butylphenol) (Di-DTP) were synthesized by the reaction of monomeric phenol derivatives with catalytic CuCl(OH). TMEDA and Na2S2O4. Their antioxidant capacity and radical scavenging activity were examined using different in vitro methodologies such as 1,1-diphenyl-2-picryl-hydrazyl (DPPH*) free radical scavenging, 2,2'-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) radical scavenging activity, total antioxidant activity by ferric thiocyanate, total reducing power by potassium ferricyanide reduction method, superoxide anion radical scavenging, hydrogen peroxide scavenging and ferrous ions chelating activities.
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Free radicals in biology and medicine
General Pharmacology The Vascular System · 1991 · 17.2K citations
Antioxidant Determinations by the Use of a Stable Free Radical
Marsden S. Blois · Nature · 1958 · 12.8K citations