Glutathione Conjugation of 4-Hydroxy-trans-2,3-nonenal in the Rat in Vivo, the Isolated Perfused Liver and Erythrocytes
- 15 September 1999
- journal article
- Published by Elsevier in Toxicology and Applied Pharmacology
- Vol. 159 (3), 214-223
- https://doi.org/10.1006/taap.1999.8742
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Identification of Novel Urinary Metabolites of the Lipid Peroxidation Product 4-Hydroxy-2-nonenal in RatsChemical Research in Toxicology, 1998
- Lipid peroxidation as a potential endogenous source for the formation of exocyclic DNA adductsCarcinogenesis: Integrative Cancer Research, 1996
- Disposition in rat of [2-3H]-trans-4-hydroxy-2,3-nonenal, a product of lipid peroxidationXenobiotica, 1996
- Synthesis of 4‐hydroxy[4‐3H]‐2(E)‐nonen‐1‐al‐diethylacetalJournal of Labelled Compounds and Radiopharmaceuticals, 1995
- Mercapturic Acid Conjugates as Urinary End Metabolites of the Lipid Peroxidation Product 4-Hydroxy-2-nonenal in the RatChemical Research in Toxicology, 1995
- Toxic aldehydes formed by lipid peroxidation I. Sensitive, gas chromatography-based stereoanalysis of 4-hydroxyalkenals, toxic products of lipid peroxidationJournal of Chromatography A, 1994
- Glutathione S‐Transferases: Structure and Mechanism of an Archetypical Detoxication EnzymePublished by Wiley ,1994
- Chemistry and biochemistry of 4-hydroxynonenal, malonaldehyde and related aldehydesFree Radical Biology & Medicine, 1991
- 4‐Hydroxyalk‐2‐enals are substrates for glutathione transferaseFEBS Letters, 1985
- Amberlyst-15, A Superior Acid Catalyst for the Cleavage of AcetalsSynthesis, 1984