Isoprenylhydroquinone glucoside: a new non-antioxidant inhibitor of peroxynitrite-mediated tyrosine nitration.
Nitric Oxide
; 12(1): 54-60, 2005 Feb.
Article
em En
| MEDLINE
| ID: mdl-15631948
ABSTRACT
Three hydroquinone glucosides and four caffeoylquinic esters were examined for their effect on tyrosine nitration, as well as on the oxidation of dihydrorhodamine (DHR) 123 and cytochrome c(2+) induced by peroxynitrite. All these phenolics, which had previously been characterized as the active principles of the plant Phagnalon rupestre, were fairly active in preventing the oxidation of DHR 123, though inefficient in the cytochrome c test. While their antioxidant potency is associated with the presence of a caffeoyl moiety, not so an obvious chemical character was correlated to a greater activity against nitration of tyrosine. Here, the highest potency corresponded to 2-isoprenylhydroquinone-1-glucoside. On the basis of the fact that the susceptibility to nitration of given aromatic compound confers to it inhibitory activity of tyrosine nitration, the analysis of ultraviolet and nuclear magnetic resonance spectral shifts provides valuable information for explaining the ability of natural phenolics to interfere with that reaction.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Tirosina
/
Ácido Peroxinitroso
/
Glucosídeos
/
Hidroquinonas
/
Nitratos
Idioma:
En
Ano de publicação:
2005
Tipo de documento:
Article