Antioxidant, prooxidant and cytotoxic activity of hydroxylated resveratrol analogues: Structure-activity relationship

Biochemical Pharmacology

Volumn 69, Issue 6, 2005, Pages 903-912

  Murias, Marek ^a   Jäger, Walter ^a   Handler, Norbert ^a   Erker, Thomas ^a   Horvath, Zsuzsanna ^a   Szekeres, Thomas ^a   Nohl, Hans ^b   Gille, Lars ^b  

^a UNIVERSITY OF VIENNA   (Austria)

^b UNIVERSITY OF VETERINARY MEDICINE   (Austria)

Author keywords

Antioxidants; Cytotoxicity; HL 60 cells; Hydroxystilbenes; Prooxidants; Resveratrol

Indexed keywords

1,1 DIPHENYL 2 PICRYLHYDRAZYL; 2 SEMIQUINONE; 3,3',4',5 TETRAHYDROXYSTILBENE; 3,3',4,4',5,5' HEXAHYDROXYSTILBENE; 3,4,4',5 TETRAHYDROXYSTILBENE; 5,5 DIMETHYL 1 PYRROLINE 1 OXIDE; OXIDIZING AGENT; OXYGEN RADICAL; RESVERATROL; SCAVENGER; SEMIQUINONE; UNCLASSIFIED DRUG;

ANIMAL TISSUE; ANTIOXIDANT ACTIVITY; ARTICLE; CELL STRAIN HL 60; CONTROLLED STUDY; DRUG HYDROXYLATION; DRUG SYNTHESIS; ELECTRON SPIN RESONANCE; HUMAN; HUMAN CELL; IC 50; LEUKEMIA CELL; MALE; MICROSOME; NONHUMAN; OXIDATION; OXIDATION REDUCTION REACTION; OXYGEN CONSUMPTION; PHOTOMETRY; PRIORITY JOURNAL; PROMYELOCYTIC LEUKEMIA; RAT; STRUCTURE ACTIVITY RELATION; SUBSTITUTION REACTION;

EID: 14644442917     PISSN: 00062952     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bcp.2004.12.001     Document Type: Article

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