Literature DB >> 3967336

Identification of the N-acetylcysteine conjugate of benzidine formed in the peroxidase activation system.

P D Josephy, D C Iwaniw.   

Abstract

Benzidine is oxidized by the peroxidase/H2O2 system, yielding reactive intermediates. In the presence of thiols, covalent adducts are formed. We used h.p.l.c. to separate the products of the reaction of benzidine with N-acetylcysteine. The major product was identified by n.m.r. spectroscopy (1H-n.m.r.) as 3-(N-acetylcystein-S-yl)-benzidine.

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Year:  1985        PMID: 3967336     DOI: 10.1093/carcin/6.1.155

Source DB:  PubMed          Journal:  Carcinogenesis        ISSN: 0143-3334            Impact factor:   4.944


  4 in total

1.  Oxidation of 4-chlorobiphenyl metabolites to electrophilic species by prostaglandin H synthase.

Authors:  Orarat Wangpradit; Lynn M Teesch; S V Santhana Mariappan; Michael W Duffel; Karin Norstrom; Larry W Robertson; Gregor Luthe
Journal:  Chem Res Toxicol       Date:  2009-01       Impact factor: 3.739

Review 2.  Prostaglandin synthase-mediated metabolism of carcinogens and a potential role for peroxyl radicals as reactive intermediates.

Authors:  L J Marnett
Journal:  Environ Health Perspect       Date:  1990-08       Impact factor: 9.031

3.  Free-radical-mediated DNA binding.

Authors:  P J O'Brien
Journal:  Environ Health Perspect       Date:  1985-12       Impact factor: 9.031

4.  Oxidative activation of benzidine and its derivatives by peroxidases.

Authors:  P D Josephy
Journal:  Environ Health Perspect       Date:  1985-12       Impact factor: 9.031

  4 in total

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