Carnosine is a quencher of 4-hydroxy-nonenal: through what mechanism of reaction?
- 1 November 2002
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 298 (5) , 699-706
- https://doi.org/10.1016/s0006-291x(02)02545-7
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Detoxification of cytotoxic α,β‐unsaturated aldehydes by carnosine: characterization of conjugated adducts by electrospray ionization tandem mass spectrometry and detection by liquid chromatography/mass spectrometry in rat skeletal muscleJournal of Mass Spectrometry, 2002
- Could carnosine be a naturally-occurring scavenger for acrolein and other reactive aldehydes in the brain?Neurobiology of Aging, 2002
- Formation of Cyclic Deoxyguanosine Adducts from ω-3 and ω-6 Polyunsaturated Fatty Acids under Oxidative ConditionsChemical Research in Toxicology, 2002
- 4-Hydroxynonenal in the Pathomechanisms of Oxidative StressIUBMB Life, 2000
- UVB-induced hemolysis of rat erythrocytes:Life Sciences, 2000
- Pluripotent Protective Effects of Carnosine, a Naturally Occurring DipeptideaAnnals of the New York Academy of Sciences, 1998
- Lipid peroxidation products and antioxidants in human disease.Environmental Health Perspectives, 1998
- The reaction of 4-hydroxy-2-nonenal with Nα-acetyl-l-histidineFree Radical Biology & Medicine, 1995
- Chemistry and biochemistry of 4-hydroxynonenal, malonaldehyde and related aldehydesFree Radical Biology & Medicine, 1991
- Ueber das Carnosin, eine neue organische Base des FleischextractesEuropean Journal of Inorganic Chemistry, 1900