Catalog No.S1354 Synonyms: A-65006, AG-1749
Molecular Weight(MW): 369.36
Lansoprazole is a proton-pump inhibitor (PPI) which prevents the stomach from producing gastric acid.
Purity & Quality Control
Choose Selective Proton Pump Inhibitors
|Description||Lansoprazole is a proton-pump inhibitor (PPI) which prevents the stomach from producing gastric acid.|
Lansoprazole inhibits gastric acid secretion via inhibition of gastric hydrogen/potassium adenosine triphosphatase (H+,K(+)-ATPase), an enzyme of the gastric parietal cell membrane that forms part of the proton pump that performs the final step in the acid secretory process. Lansoprazole binds covalently to parietal cell H+,K(+)-ATPase, rendering it nonfunctional and inhibiting the secretion of gastric acid.  Lansoprazole is a strong anti-secretory agent that acts on gastric H+/K+-adenosine triphosphatase (H+/K+ ATPase) of parietal cells. Lansoprazole inhibits the increased expression of vascular adhesion molecules, the activation of neutrophils, and the production of pro-inflammatory cytokines from activated endothelial cells. Lansoprazole induces several genes, including phase II detoxifying enzyme (NADPH-ubiquinone oxidoreductase, glutathione S-transferase) and antioxidant stress proteins (HO-1, thioredoxin reductase, and superoxide dismutase) in gastric epithelial cells. Lansoprazole significantly inhibits the production of CINC-1 from stimulated RGM-1 cells with IL-1β. Lansoprazole up-regulates HO-1 expression throughout Nrf2 in rat gastric epithelial cells, and the up-regulated HO-1 has anti-inflammatory effects. 
|In vivo||Lansoprazole inhibits acute inflammatory reactions as well as intestinal mucosal injuries induced by ischemia-reperfusion or indomethacin administration in rats. Lansoprazole significantly inhibits intestinal injuries induced by ischemia-reperfusion or indomethacin. lansoprazole administered exogenously prevents the small intestine against ischemia-reperfusion or indomethacin-induced damage, the action being dependent on its anti-inflammatory and anti-oxidative responses. |
|In vitro||DMSO||74 mg/mL (200.34 mM)|
|Ethanol||14 mg/mL (37.9 mM)|
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.
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* When preparing stock solutions always use the batch-specific molecular weight of the product found on the vial label and MSDS / COA (available online).
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Clinical Trial Information
|NCT Number||Recruitment||interventions||Conditions||Sponsor/Collaborators||Start Date||Phases|
|NCT02442752||Suspended||Drug: Dexlansoprazole||Pediatric Gastroesophageal Reflux Disease||Takeda||June 15 2025||Phase 1|
|NCT03316976||Completed||Drug: Dexlansoprazole||Healthy Volunteers||Takeda||November 22 2017||Phase 1|
|NCT03079050||Completed||Drug: Dexlansoprazole 60 MG||GERD|Proton Pump Inhibitor||American University of Beirut Medical Center|Takeda||February 27 2017||Phase 4|
Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.
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