| Literature DB >> 3967336 |
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.Entities:
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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