JOURNAL ARTICLE

Antioxidant properties of the decarboxylated dimer of aminoethylcysteine ketimine: Assessment of its ability to scavenge peroxynitrite

Mario FontanaLaura PecciAlberto MaconeDoriàno Cavallini

Year: 1998 Journal:   Free Radical Research Vol: 29 (5)Pages: 435-440   Publisher: Taylor & Francis

Abstract

The natural sulfur compound aminoethylcysteine ketimine decarboxylated dimer (AECK dimer) has been investigated for its ability to act as peroxynitrite scavenger. It has been found that the product efficiently protects against the nitration of tyrosine and the inactivation of alpha1-antiproteinase by peroxynitrite. The tyrosine nitration can be completely prevented by 100 microM AECK dimer which appears as effective as the antioxidants glutathione and N-acetylcysteine. The AECK dimer was also found to limit surface charge alteration of low density lipoprotein induced by peroxynitrite. These findings indicate that the AECK dimer is a strong protective agent against peroxynitrite damage and that it could play an important role in the defence against oxidative stress in human diseases.

Keywords:
Peroxynitrite Chemistry Dimer Nitration Antioxidant Tyrosine Biochemistry Glutathione Peroxynitrous acid Oxidative stress Photochemistry Superoxide Enzyme Organic chemistry

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23
Cited By
1.30
FWCI (Field Weighted Citation Impact)
34
Refs
0.76
Citation Normalized Percentile
Is in top 1%
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Citation History

Topics

Free Radicals and Antioxidants
Physical Sciences →  Chemistry →  Organic Chemistry
Nitric Oxide and Endothelin Effects
Health Sciences →  Medicine →  Physiology
Eicosanoids and Hypertension Pharmacology
Life Sciences →  Biochemistry, Genetics and Molecular Biology →  Biochemistry
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