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Lansoprazole

Catalog No. T0674Cas No. 103577-45-3
Alias AG-1749, A-65006

Lansoprazole (A-65006) is a 2, 2, 2-trifluoroethoxypyridyl derivative of timoprazole that is used in the therapy of STOMACH ULCERS and ZOLLINGER-ELLISON SYNDROME. The drug inhibits H(+)-K(+)-EXCHANGING ATPASE which is found in GASTRIC PARIETAL CELLS. Lansoprazole is a potent brain penetrant neutral sphingomyelinase (N-SMase) inhibitor (exosome inhibitor)

Lansoprazole

Lansoprazole

Purity: 99.84%
Catalog No. T0674Alias AG-1749, A-65006Cas No. 103577-45-3
Lansoprazole (A-65006) is a 2, 2, 2-trifluoroethoxypyridyl derivative of timoprazole that is used in the therapy of STOMACH ULCERS and ZOLLINGER-ELLISON SYNDROME. The drug inhibits H(+)-K(+)-EXCHANGING ATPASE which is found in GASTRIC PARIETAL CELLS. Lansoprazole is a potent brain penetrant neutral sphingomyelinase (N-SMase) inhibitor (exosome inhibitor)
Pack SizePriceAvailabilityQuantity
500 mg$45In Stock
1 g$62In Stock
1 mL x 10 mM (in DMSO)$50In Stock
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Purity:99.84%
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Product Introduction

Bioactivity
Description
Lansoprazole (A-65006) is a 2, 2, 2-trifluoroethoxypyridyl derivative of timoprazole that is used in the therapy of STOMACH ULCERS and ZOLLINGER-ELLISON SYNDROME. The drug inhibits H(+)-K(+)-EXCHANGING ATPASE which is found in GASTRIC PARIETAL CELLS. Lansoprazole is a potent brain penetrant neutral sphingomyelinase (N-SMase) inhibitor (exosome inhibitor)
In vitro
Lansoprazole significantly attenuates intestinal damage induced by ischemia-reperfusion or indomethacin. Exogenous administration of Lansoprazole can prevent injury to the small intestine caused by ischemia-reperfusion or indomethacin. Lansoprazole inhibits acute inflammatory responses and mucosal injury in rats subjected to ischemia-reperfusion or indomethacin-induced damage.
In vivo
Lansoprazole is a potent antisecretory agent that inhibits gastric acid secretion by blocking the stomach's hydrogen/potassium adenosine triphosphatase (H+, K+-ATPase). It suppresses the upregulation of adhesion molecules in blood vessels, neutrophil activation, and the production of pro-inflammatory cytokines from activated endothelial cells. Furthermore, Lansoprazole induces the expression of various genes in gastric epithelial cells, including Phase II detoxifying enzymes (NADPH-quinone oxidoreductase, glutathione S-transferase) and antioxidative stress proteins (HO-1, thioredoxin reductase, and superoxide dismutase). In rat gastric epithelial cells, Lansoprazole upregulates HO-1 expression and exerts anti-inflammatory effects.
AliasAG-1749, A-65006
Chemical Properties
Molecular Weight369.36
FormulaC16H14F3N3O2S
Cas No.103577-45-3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
1eq. HCl: 18.5 mg/mL (50 mM)
DMSO: 50 mg/mL (135.37 mM)
Solution Preparation Table
1eq. HCl/DMSO
1mg5mg10mg50mg
1 mM2.7074 mL13.5369 mL27.0739 mL135.3693 mL
5 mM0.5415 mL2.7074 mL5.4148 mL27.0739 mL
10 mM0.2707 mL1.3537 mL2.7074 mL13.5369 mL
20 mM0.1354 mL0.6768 mL1.3537 mL6.7685 mL
50 mM0.0541 mL0.2707 mL0.5415 mL2.7074 mL
DMSO
1mg5mg10mg50mg
100 mM0.0271 mL0.1354 mL0.2707 mL1.3537 mL

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