Enantioselective disposition of rabeprazole in relation to CYP2C19 genotypes
Author:
Publisher
Wiley
Subject
Pharmacology (medical),Pharmacology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2125.2005.02566.x/fullpdf
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1. Rabeprazole
2. The potency of substituted benzimidazoles such as E3810, omeprazole, RO 18-5364 to inhibit gastric H+,K+-ATPase is correlated with the rate of acid-activation of the inhibitor
3. Inhibitions of acid secretion by E3810 and omeprazole, and their reversal by glutathione
4. Review article: cytochrome P450 and the metabolism of proton pump inhibitors - emphasis on rabeprazole
5. Comparison of the kinetic disposition and metabolism of E3810, a new proton pump inhibitor, and omeprazole in relation to S-mephenytoin 4′-hydroxylation status
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