Valpromide is a poor inhibitor of the cytosolic epoxide hydrolase
Author:
Publisher
Springer Science and Business Media LLC
Subject
Health, Toxicology and Mutagenesis,Toxicology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/BF00316440.pdf
Reference18 articles.
1. Gill SS, Hammock BD (1980) Distribution and properties of a mammalian soluble epoxide hydrase. Biochem Pharmacol 29: 389?395
2. Guenthner TM, Hammock BD, Vogel U, Oesch F (1981) Cytosolic and microsomal epoxide hydrase are immunologically distinguishable from each other in the rat and mouse. J Biol Chem 256: 3163?3165
3. Hammock BD, Ota K (1983) Differential induction of cytosolic epoxide hydrolase, microsomal epoxide hydrolase and glutathione S-trans-ferase activities. Toxicol Appl Pharmacol 71: 254?256
4. Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with Folin phenol reagent. J Biol Chem 193: 265?275
5. Mertes I, Fleischmann R, Glatt HR, Oesch F (1985) Interindividual variations in the activities of cytosolic and microsomal epoxide hydrolase in human liver. Carcinogenesis 6: 219?223
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