Literature DB >> 3439889

The metabolic origin of the sulfur atom in the sulfhydryl group of 2-thiobenzothiazole metabolites derived from benzothiazyl sulfenamide in the rat.

M Fukuoka1, A Tanaka.   

Abstract

After administration of benzothiazyl sulfenamide to rats, over 90% of the S atom in the sulfhydryl group was retained in 2-thiobenzothiazole metabolites. The S atom in 2-benzothiazyl mercapturic acid, a major metabolite, was mostly replaced by the endogenous S from the L-cysteine pool.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 3439889     DOI: 10.1007/BF00661376

Source DB:  PubMed          Journal:  Arch Toxicol        ISSN: 0340-5761            Impact factor:   5.153


  2 in total

1.  THE BIOTRANSFORMATION OF A SULFONAMIDE TO A MERCAPTAN AND TO MERCAPTURIC ACID AND GLUCURONIDE CONJUGATES.

Authors:  D F COLUCCI; D A BUYSKE
Journal:  Biochem Pharmacol       Date:  1965-04       Impact factor: 5.858

2.  Acquirement of fetal properties in hepatoma on glutathione metabolism.

Authors:  N Taniguchi; Y Tsukada; H Hirai
Journal:  Biochim Biophys Acta       Date:  1974-07-04
  2 in total
  1 in total

1.  Metabolism of 2-thiobenzothiazoles in the rat. Urinary, fecal and biliary metabolites of 2-benzothiazyl sulfenamides.

Authors:  M Fukuoka; M Satoh; A Tanaka
Journal:  Arch Toxicol       Date:  1995       Impact factor: 5.153

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.