The fate ofS-propylcysteine in the rat
- 1 January 1980
- journal article
- research article
- Published by Taylor & Francis in Xenobiotica
- Vol. 10 (11) , 827-834
- https://doi.org/10.3109/00498258009033813
Abstract
1. The metabolism of S-propylcysteine in the rat has been re-investigated. The previously known major metabolite has been isolated and identified as the mercapturic acid, N-acetyl-S-propylcysteine. 2. Several further metabolites have been isolated from the urine of rats treated with S-propyl[35S]cysteine. These have been identified as S-propylcysteine-S-oxide, N-acetyl-S-(2-hydroxypropyl)cysteine, S-(propylthio)lactate, S-(2,3-dihydroxypropyl)cysteine and N-acetyl-S-(2-carboxyethyl)cysteine. 3. The metabolism of S-(2-hydroxypropyl)-, S-(3-hydroxypropyl)- and S-(2,3-dihydroxypropyl)[35S]cysteine have been investigated in the rat. The results, integrated with those from the metabolism of S-propyl[35S]cysteine, have enabled the pathways of S-propylcysteine to be deduced. 4. The oxidative metabolism of a number of S-alkyl cysteines is discussed.This publication has 22 references indexed in Scilit:
- The Oxidative Metabolism of 1-Bromopropane in the RatXenobiotica, 1979
- Mercapturic Acid Formation in the Developing RatXenobiotica, 1977
- The Metabolism of 3-Chloro-, 3-Bromo- and 3-Iodopropan-1,2-diol in Rats and MiceXenobiotica, 1975
- Some Metabolites ofS-Pentyl-L-cysteine in the Rabbit and Other SpeciesXenobiotica, 1973
- Studies with alkylating esters—IV: The metabolism of propane-1,3-dimethanesulphonate and its relevance to the mode of action of myleranBiochemical Pharmacology, 1971
- The acetylation of S-alkylcysteines by the ratBiochemical Pharmacology, 1969
- α-Hydroxy acids as metabolites of sulfur amino acids in yeastArchives of Biochemistry and Biophysics, 1966
- The metabolism of S-methyl-l-cysteine in the ratBiochimica et Biophysica Acta (BBA) - General Subjects, 1964
- Techniques and Reagents for Paper ChromatographyAnalytical Chemistry, 1951
- Die Synthese des natürlichen Alliins und seiner drei optisch aktiven Isomeren. 5. Mitteilung über Allium‐SubstanzenHelvetica Chimica Acta, 1951