Biological and Pharmaceutical Bulletin · 2005 · 124 citations · 12 references
MedicineBiochemistryAntimicrobial PharmacologyBiochemical PharmacologyStructure-activity RelationshipsAntiviral AgentsAntiviral PharmacologyAbsolute Configuration AssignmentAbsolute Configuration DeterminationAntiviral Marine CompoundsCytomegalovirus DiseaseFree Radical ScavengingMarine-derived Antiviral CompoundsPlastoquinone Chemistry
Two plastoquinones were isolated from the methanolic extract of the brown alga Sargassum micracanthum, and these were identified as a known 2-geranylgeranyl-6-methylbenzoquinone and its hydroquinone, respectively, based on spectroscopic analysis. The absolute configuration of the secondary hydroxyl group was determined by the modified Mosher's method using the new chromene derivative converted from plastoquinones. One of the plastoquinones and the chromene exhibited significant antioxidant activities, such as an inhibitory effect on lipid peroxidation and a radical scavenging effect on 1,1-diphenyl-2-picrylhydrazyl (DPPH). The benzoquinone-type compound and the chromene derivative were found to have potent antiviral activity against human cytomegalovirus (HCMV).
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Antioxidant Determinations by the Use of a Stable Free Radical
Marsden S. Blois · Nature · 1958 · 12.8K citations
Thomas C. Pederson, John A. Buege, Steven D. Aust · Journal of Biological Chemistry · 1973 · 327 citations · Full text