(Q28373001)

2

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J Alary

3

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L Debrauwer

4

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J P Cravedi

Mercapturic acid conjugates as urinary end metabolites of the lipid peroxidation product 4-hydroxy-2-nonenal in the rat

5

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language of work or name

English

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publication date

3 April 2000

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published in

Toxicology Letters

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volume

114

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issue

1-3

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page(s)

203-14

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cites work

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Identification of novel urinary metabolites of the lipid peroxidation product 4-hydroxy-2-nonenal in rats

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Inhibition of medium-chain fatty acid beta-oxidation in vitro by valproic acid and its unsaturated metabolite, 2-n-propyl-4-pentenoic acid

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Physiological substrates for rat alcohol dehydrogenase classes: aldehydes of lipid peroxidation, omega-hydroxyfatty acids, and retinoids

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2,3-epoxy-4-hydroxynonanal as a potential tumor-initiating agent of lipid peroxidation.

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Past, present, and future applications of precision-cut liver slices for in vitro xenobiotic metabolism

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Metabolism of the lipid peroxidation product 4-hydroxynonenal by isolated hepatocytes and by liver cytosolic fractions

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Chemistry and biochemistry of 4-hydroxynonenal, malonaldehyde and related aldehydes

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The hepatocellular metabolism of 4-hydroxynonenal by alcohol dehydrogenase, aldehyde dehydrogenase, and glutathione S-transferase

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Rat glutathione transferase 8-8, an enzyme efficiently detoxifying 4-hydroxyalk-2-enals

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Comparison of the inactivation of microsomal glucose-6-phosphatase by in situ lipid peroxidation-derived 4-hydroxynonenal and exogenous 4-hydroxynonenal

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In vitro effects of trans-4-hydroxy-2-alkenals on mouse liver cytochrome P-450

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The oxidation of alpha-beta unsaturated aldehydic products of lipid peroxidation by rat liver aldehyde dehydrogenases

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Separation and characterization of the aldehydic products of lipid peroxidation stimulated by carbon tetrachloride or ADP-iron in isolated rat hepatocytes and rat liver microsomal suspensions

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Lipid peroxidation product, 4-hydroxynonenal and its conjugate with GSH are excellent substrates of bovine lens aldose reductase

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