A comparison of the hydroxyl radical scavenging properties of the shark bile steroid 5β‐scymnol and plant pycnogenols

The hydroxyl radical (OH·) quenching abilities of the following compounds were compared in the deoxyribose degradation system (initiated by the ferrous‐ascorbate Fenton reaction): (a) 5β‐scymnol, the hepatoprotective shark bile sterol, and its mono‐ and di‐sulfate esters; (b) three marketed pycnogen...

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Veröffentlicht in:	Biochemistry and molecular biology international 1997-09, Vol.42 (6), p.1249-1260
Hauptverfasser:	Macrides, Theodore A., Shihata, Amal, Kalafatis, Nicolette, Wright, Paul F. A.
Format:	Artikel
Sprache:	eng
Schlagworte:	Animals Antioxidants - pharmacology Ascorbic Acid - metabolism Bile - chemistry Bile Acids and Salts - isolation & purification Bile Acids and Salts - pharmacology Cholestanols - chemistry Cholestanols - pharmacology Chromatography, High Pressure Liquid Deoxyribose - metabolism Ferrous Compounds - metabolism Flavonoids - pharmacology Free Radical Scavengers - chemistry Free Radical Scavengers - pharmacology Hydroxyl Radical Plants - chemistry Sharks Sulfates
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