Release Time:2019-03-09  Hits:

Indexed by: Journal Article

Date of Publication: 2010-11-01

Journal: CHEMICAL RESEARCH IN CHINESE UNIVERSITIES

Included Journals: Scopus、CSCD、ISTIC、SCIE

Volume: 26

Issue: 6

Page Number: 981-985

ISSN: 1005-9040

Key Words: Liver microsome; Reduction; Nitroaromatic compound; Aromatic hydroxylamine

Abstract: Nitroaromatic compounds were reductively metabolized to the corresponding amine compounds via the intermediate hydroxylamines by liver microsomes from pig, rat, chook, cattle, sheep, paralichthys olivaceus and cyprinoid in varied reactivity. Similar with baker's yeast, the pig, rat and sheep liver microsomes exhibited high reactivity toward 4-nitro-1,2-dicyanbenzen(1a), while the cyprinoid liver microsomes were inefficient. Contrasted to compound la, monocyannitrobenzene(2a) was difficult to reduce by pig liver microsomes. In opposition to grape cells, pig liver microsomes exhibited activities toward some aromatic hydroxylamine compounds.