Substituted thieno[3,4-d]imidazoles, a novel group of H+/K+-ATPase inhibitors. Differentiation of their inhibition characteristics from those of omeprazole

Author:

Beil Winfried,Staar Ute,Sewing Karl-Friedrich

Publisher

Elsevier BV

Subject

Pharmacology

Reference22 articles.

1. Omeprazole, SCH 28080 and doxepin differ in their characteristics to inhibit H+/K+-ATPase driven proton accumulation by parietal cell membrane vesicles;Beil;Biochem. Pharmacol.,1988

2. Inorganic phosphate assay with malachite green: an improvement and evaluation;Carter;J. Biochem. Biophys. Meth.,1982

3. Omeprazole. A preliminary review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in peptic ulcer disease and Zollinge r-Ellison syndrome;Clissold;Drugs,1986

4. Coupling of H+-K+-ATPase activity and glucose oxidation in gastric glands;Fryklund;Am. J. Physiol.,1990

5. Substituted thieno [3.4-d] imidazoles as H+, K+-ATPase inhibitors with a different inhibitory profile compared with omeprazole;Herling;Gastroenterology,1989

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