Oxidation of dopamine by peroxyl radicals-A commentary on the site of radical attack

Free Radical Biology and Medicine

Volumn 42, Issue 5, 2007, Pages 730-

  Litwinienko, Grzegorz ^a   Ingold, Keith U ^b  

^a UNIVERSITY OF WARSAW   (Poland)

^b NATIONAL RESEARCH COUNCIL CANADA   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

DOPAMINE; PEROXY RADICAL;

BRAIN; CHEMICAL REACTION; DEGENERATIVE DISEASE; LETTER; MOLECULAR BIOLOGY; MOLECULAR MECHANICS; NEUROCHEMISTRY; OXIDATION; OXIDATIVE STRESS; PARKINSON DISEASE; PEROXIDATION; PRIORITY JOURNAL;

DOPAMINE; FREE RADICALS; MODELS, BIOLOGICAL; OXIDATION-REDUCTION; PEROXIDES;

EID: 33846798048     PISSN: 08915849     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.freeradbiomed.2006.09.029     Document Type: Letter

References (7)

1. Spiteller G. Peroxyl radicals: inductors of neurodegenerative and other inflammatory diseases. Their origin and how they transform cholesterol, phospholipids, plasmalogens, polyunsaturated fatty acids, sugars, and proteins into deleterious products. Free Radic. Biol. Med. 41 (2006) 362-387
2. Spiteller G. Linoleic acid peroxidation-The dominant lipid peroxidation process in low density lipoprotein-And its relationship to chronic diseases. Chem. Phys. Lipids 95 (1998) 105-162
3. Bielski B. H. J., Reaction rates of superoxide radicals with the essential amino acids. Oxygen free radicals and tissue damage. Ciba Foundation Symposium 65, N. S. Amsterdam: Excerpta Medica; 1979: 43-56.
4. Griller D., Howard J.A., Marriott P.R., and Scaiano J.C. Absolute rate constants for the reactions of tert-butoxyl, tert-butylperoxyl, and benzophenone triplet with amines: the importance of a stereoelectronic effect. J. Am. Chem. Soc. 103 (1981) 619-623
5. Tavadyan L.A., Musaelyan M.V., and Mardoyan V.A. Tertiary butyl peroxyl radical reactivity towards aliphatic amines in a liquid phase. Sov. J. Chem. Phys. (English translation) 8 (1991) 1358-1366
6. Foti M.C., Johnson E.R., Vinqvist M.R., Wright J.S., Barclay L.R.C., and Ingold K.U. Naphthalene diols: a new class of antioxidants. intramolecular hydrogen bonding in catechols, naphthalene diols, and their aryloxyl radicals. J. Org. Chem. 67 (2002) 5190-5196
7. Burton G.W., Doba T., Gabe E.J., Hughes L., Lee F.L., Prasad L., and Ingold K.U. Autoxidation of biological molecules. 4. Maximizing the antioxidant activity of phenols. J. Am. Chem. Soc. 107 (1985) 7053-7065