Xenobiotica 1998-10-01

Intermediary metabolism of pentachloronitrobenzene in the control and germ-free rat and rat with cannulated bile ducts.

G L Larsen, J K Huwe, J E Bakke

Index: Xenobiotica 28(10) , 973-84, (1998)

Full Text: HTML

Abstract

1. Nearly 70% of single oral doses of 14C-labelled pentachloronitrobenzene (PCNB) was excreted in bile within 24 h. 2. The characterized biliary metabolites of PCNB were either mercapturic acid pathway metabolites or catabolites thereof (thiols, methylthiols, S-glucuronides). 3. A major biliary metabolite was S-(aminotetrachlorophenyl)glutathione. 4. Conjugation with glutathione with subsequent catabolism to bis-methylthiotetrachlorobenzene was the major pathway in the control rat. 5. Germ-free experiments showed that only nitro- group displacement occurred, and no nitro- group reduction was detected.

Related Compounds

Structure Name/CAS No. Articles
Pentachloronitrobenzene Structure Pentachloronitrobenzene
CAS:82-68-8
Pentachloroaniline Structure Pentachloroaniline
CAS:527-20-8