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omeprazole sulfide

Known as: omeprazole sulphide 
 
National Institutes of Health

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Broader (1)

Omeprazole
analogs & derivatives

Papers overview

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2017
2017
Disposition of the anti-ulcer medications ranitidine, cimetidine, and omeprazole following administration of multiple doses to exercised Thoroughbred horses.
The use of anti-ulcer medications, such as cimetidine, ranitidine, and omeprazole, is common in performance horses. The use of… Expand
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2016
2016
Regioselective C-H hydroxylation of omeprazole sulfide by Bacillus megaterium CYP102A1 to produce a human metabolite
ObjectivesTo find a simple enzymatic strategy for the efficient synthesis of the expensive 5′-hydroxyomeprazole sulfide, a… Expand
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2014
2014
Simultaneous determination of omeprazole and their main metabolites in human urine samples by capillary electrophoresis using electrospray ionization-mass spectrometry detection.
We report a novel method for the simultaneous determination of omeprazole and their main metabolites (omeprazole sulphide… Expand
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2013
2013
Investigating the presence of omeprazole in waters by liquid chromatography coupled to low and high resolution mass spectrometry: degradation experiments.
Omeprazole is one of the most consumed pharmaceuticals around the world. However, this compound is scarcely detected in urban… Expand
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2013
2013
Solubility of Omeprazole Sulfide in Different Solvents at the Range of 280.35–319.65 K
Solubility data were measured for omeprazole sulfide in ethanol, 95 mass-% ethanol, ethyl acetate, isopropanol, methanol, acetone… Expand
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2011
2011
Whole-cell oxidation of omeprazole sulfide to enantiopure esomeprazole with Lysinibacillus sp. B71.
Production of enantiopure esomeprazole by biocatalysis is of great demand by pharmaceutical industry. A Gram-positive bacterium… Expand
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Highly Cited
2006
Highly Cited
2006
Role of CYP3A4 in the regulation of the aryl hydrocarbon receptor by omeprazole sulphide.
Cross-talk between nuclear receptors involved in the control of drug metabolism is being increasingly recognised as a source of… Expand
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1987
1987
Inhibition of gastric K+/H+-ATPase by acid-activated 2-((2-pyridylmethyl)sulphinyl)benzimidazole products.
The inhibitory effects of timoprazole- and omeprazole-derived metabolites were studied in different in vitro test systems in… Expand
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Highly Cited
1985
Highly Cited
1985
Omeprazole, a specific inhibitor of gastric (H+-K+)-ATPase, is a H+-activated oxidizing agent of sulfhydryl groups.
Omeprazole (5-methoxy-2-[[(4-methoxy-3,5- dimethylpyridinyl)methyl]sulfinyl]-1H-benzimidazole) appeared to inhibit gastric (H+-K… Expand
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1983
1983
Simultaneous high-performance liquid chromatographic analysis of omeprazole and its sulphone and sulphide metabolites in human plasma and urine.
Omeprazole, a substituted benzimidazole which suppresses gastric acid secretion, and its sulphone and sulphide metabolites were… Expand
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