An essential difference in the reactivity of the glutathione adducts of the structurally closely related flavonoids monoHER and quercetin

Free Radical Biology and Medicine

Volumn 51, Issue 11, 2011, Pages 2118-2123

  Jacobs, Hilde ^a   Moalin, Mohamed ^a,b   Van Gisbergen, Marike W ^a   Bast, Aalt ^a   Van Der Vijgh, Wim J F ^a   Haenen, Guido R M M ^a  

^a MAASTRICHT UNIVERSITY MEDICAL CENTER   (Netherlands)

^b ZUYD UNIVERSITY OF APPLIED SCIENCES   (Netherlands)

Author keywords

7 Mono O ( hydroxyethyl)rutoside; Antioxidant; Flavonoid; Free radicals; Glutathione; MonoHER; Quercetin; Thiols

Indexed keywords

ACETYLCYSTEINE; DISULFIDE; DITHIOL DERIVATIVE; DITHIOTHREITOL; GLUTATHIONE; MONOXERUTIN; QUERCETIN; QUINONE DERIVATIVE;

ARTICLE; CONJUGATE; CONTROLLED STUDY; PRIORITY JOURNAL; QUANTUM CHEMISTRY;

GLUTATHIONE; HYDROXYETHYLRUTOSIDE; MOLECULAR STRUCTURE; QUERCETIN; SULFHYDRYL COMPOUNDS;

EID: 80255136353     PISSN: 08915849     EISSN: 18734596     Source Type: Journal    
DOI: 10.1016/j.freeradbiomed.2011.09.013     Document Type: Article

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