Skip to main content
NCBI home page
Biochemical Journal logoLink to Biochemical Journal
. 1958 Sep;70(1):111–119. doi: 10.1042/bj0700111

Biochemical studies of toxic agents. 11. The occurrence of premercapturic acids*

R H Knight 1, L Young 1
PMCID: PMC1196634  PMID: 13584310

Full text

PDF
111

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. AZOUZ W. M., PARKE D. V., WILLIAMS R. T. Studies in detoxication. 62. The metabolism of halogenobenzenes; ortho- and para-dichlorobenzenes. Biochem J. 1955 Mar;59(3):410–415. doi: 10.1042/bj0590410. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. BOYLAND E., SIMS P. Metabolism of polycyclic compounds. 12. An acid-labile precursor of 1-naphthylmercapturic acid and naphthol: an N-acetyl-S-(1:2-dihydrohydroxy-naphthyl)-L-cysteine. Biochem J. 1958 Mar;68(3):440–447. doi: 10.1042/bj0680440. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. BOYLAND E., SOLOMON J. B. Metabolism of polycyclic compounds. X. Estimation of metabolites of naphthalene by paper chromatography. Biochem J. 1956 Aug;63(4):679–683. doi: 10.1042/bj0630679. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. BOYLAND E., SOLOMON J. B. Metabolism of polycylic compounds. 8. Acid-labile precursors of naphthalene produced as metabolites of naphthalene. Biochem J. 1955 Mar;59(3):518–522. doi: 10.1042/bj0590518. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. BRAY H. G., JAMES S. P., THORPE W. V. The metabolism of the monochloronitrobenzenes in the rabbit. Biochem J. 1956 Sep;64(1):38–44. doi: 10.1042/bj0640038. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Booth J., Boyland E. Metabolism of polycyclic compounds. 5. Formation of 1:2-dihydroxy-1:2-dihydronaphthalenes. Biochem J. 1949;44(3):361–365. [PMC free article] [PubMed] [Google Scholar]
  7. Bourne M. C., Young L. The metabolism of naphthalene in rabbits. Biochem J. 1934;28(3):803–808. doi: 10.1042/bj0280803. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Boyland E., Levi A. A. Metabolism of polycyclic compounds: Anthrylmercapturic acid. Biochem J. 1936 Jul;30(7):1225–1227. doi: 10.1042/bj0301225. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. CORNER E. D., BILLETT F. S., YOUNG L. Biochemical studies of toxic agents. 6. The conversion of naphthalene into 1:2-dihydro-2-hydroxy-1-naphthyl glucosiduronic acid in the rabbit. Biochem J. 1954 Feb;56(2):270–274. doi: 10.1042/bj0560270. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. CORNER E. D., YOUNG L. Biochemical studies of toxic agents. 8. 1:2-Dihydronaphthalene-1:2-diol and its role in the metabolism of naphthalene. Biochem J. 1955 Sep;61(1):132–141. doi: 10.1042/bj0610132. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Elson L. A., Goulden F., Warren F. L. The urinary partition of sulphur in rats treated with aromatic hydrocarbons, with special reference to growth retardation. Biochem J. 1945;39(4):301–308. doi: 10.1042/bj0390301. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. FEWSTER M. E., HALL D. A. Application of buffered solvent systems to the detection of aromatic acids by paper partition chromatography. Nature. 1951 Jul 14;168(4263):78–79. doi: 10.1038/168078a0. [DOI] [PubMed] [Google Scholar]
  13. HAWKINS J. B., YOUNG L. Biochemical studies of toxic agents. V. Observations on the fate of 35S-labelled arylsulphuric acids following their administration of the rat. Biochem J. 1954 Jan;56(1):166–170. doi: 10.1042/bj0560166. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. MARSDEN C. M., YOUNG L. Biochemical studies of toxic agents. 10. Observations on the metabolism of 35S-labelled mercapturic acids. Biochem J. 1958 Jun;69(2):257–265. doi: 10.1042/bj0690257. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Young L. The metabolic conversion of naphthalene to 1:2-dihydronaphthalene-1:2-diol. Biochem J. 1947;41(3):417–422. doi: 10.1042/bj0410417. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Biochemical Journal are provided here courtesy of The Biochemical Society

RESOURCES