The melatonin metaboliteN1-acetyl-5-methoxykynuramine is a potent singlet oxygen scavenger
Author:
Publisher
Wiley
Subject
Endocrinology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-079X.2008.00614.x/fullpdf
Reference20 articles.
1. Antioxidant properties of the melatonin metabolite N1-acetyl-5-methoxykynuramine (AMK): scavenging of free radicals and prevention of protein destruction;Ressmeyer;Redox Rep,2003
2. Photocatalytic actions of the pesticide metabolite 2-hydroxyquinoxaline: destruction of antioxidant vitamins and biogenic amines - implications of organic redox cycling;Behrends;Redox Rep,2004
3. Reactions of the melatonin metabolite AMK (N1-acetyl-5-methoxykynuramine) with reactive nitrogen species: formation of novel compounds, 3-acetamidomethyl-6-methoxycinnolinone and 3-nitro-AMK;Guenther;J Pineal Res,2005
4. N1-acetyl-5-methoxykynuramine contrasts with other tryptophan metabolites by a peculiar type of NO scavenging: cyclization to a cinnolinone prevents formation of unstable nitrosamines;Hardeland;J Pineal Res,2007
5. Reactions of the NO redox forms NO+, ·NO and HNO (protonated NO-) with the melatonin metabolite N1-acetyl-5-methoxykynuramine (AMK);Hardeland;J Pineal Res,2007
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