Omeprazole, SCH 28080 and doxepin differ in their characteristics to inhibit H+/K+-ATPase driven proton accumulation by parietal cell membrane vesicles-Reference-Cited by-同舟云学术

Omeprazole, SCH 28080 and doxepin differ in their characteristics to inhibit H+/K+-ATPase driven proton accumulation by parietal cell membrane vesicles

Published:1988-12 Issue:23 Volume:37 Page:4487-4493
ISSN:0006-2952
Container-title:Biochemical Pharmacology
language:en
Short-container-title:Biochemical Pharmacology

Author:

Beil Winfried,Staar Ute,Schünemann Petra,Sewing K.-FR.

Publisher

Elsevier BV

Subject

Pharmacology,Biochemistry

Reference20 articles.

1. Inhibition of gastric acid secretion by omeprazole, cimetidine and SCN. Differentiation of their inhibition characteristics in vitro;Wallmark;Am J Physiol,1983

2. Mechanism of gastric antisecretory effect of SCH 28080;Beil;Br J Pharmacol,1986

3. Inhibition of gastric H+,K+-ATPase and acid secretion by SCH 28080, a substituted pyridyl (1,2a) imidazole;Wallmark;J Biol Chem,1987

4. Studies on the mechanism of action of the gastric microsomal (H+ + K+)-ATPase inhibitors SCH 32651 and SCH 28080;Scott;Biochem Pharmacol,1987

5. Inhibition of (H+ + K+)-ATPase and H+ accumulation in hog gastric membranes by trifluoperazine, verapamil and 8-(N, N-diethy(amino)octyl-3,4,5-trimethoxy-benzoate;Im;Biochim Biophys Acta,1984

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1. Inhibition of gastric H+,K+-ATPase by 4-(2-butyl-6,7-dichloro-2-cyclopentylindan-1-on-5-yl)oxybutyric acid (DCPIB), an inhibitor of volume-regulated anion channel;European Journal of Pharmacology;2015-10

2. Helicobacter pylori augments the acid inhibitory effect of omeprazole on parietal cells and gastric H+/K+-ATPase;Gut;2001-02-01

3. Interaction of Helicobacter pylori and its fatty acids with parietal cells and gastric H+/K(+)-ATPase.;Gut;1994-09-01

4. Imidazole derivatives, part IX selective reactions of functionalized imidazo[1,2-a]pyridines: stereospecific synthesis of 5,6-dihydroimidazo[1,2-a]pyridines;Tetrahedron Letters;1994-04

5. 4 Gastric H+/K+-ATPase Inhibitors;Progress in Medicinal Chemistry;1994