Home Transmembrane Transporters Proton Pump inhibitor - ATPase inhibitor Pantoprazole sodium For research use only.

Pantoprazole sodium

Synonyms: SKF96022 sodium, BY-1023 sodium

Pantoprazole (SKF96022, BY-1023) is a proton pump inhibitor drug that inhibits gastric acid secretion. It works on gastric parietal cells to irreversibly inhibit (H+/K+)-ATPase function and suppress the production of gastric acid.

Pantoprazole sodium Chemical Structure

Pantoprazole sodium Chemical Structure

CAS: 138786-67-1

Selleck's Pantoprazole sodium has been cited by 2 publications

Purity & Quality Control

Batch: Purity: 99.85%
99.85

Pantoprazole sodium Related Products

Signaling Pathway

Proton Pump Signaling Pathways

Proton Pump Signaling Pathway

Choose Selective Proton Pump Inhibitors

Biological Activity

Description Pantoprazole (SKF96022, BY-1023) is a proton pump inhibitor drug that inhibits gastric acid secretion. It works on gastric parietal cells to irreversibly inhibit (H+/K+)-ATPase function and suppress the production of gastric acid.
Targets
Proton pump [4] HIF-1α [2] (H+/K+)-ATPase [4]
In vitro
In vitro pantoprazole (PPZ) inhibits tumor cells proliferation, inducs apoptosis and decreases the expression of HIF-1α protein[2]. Pantoprazole affects the intracellular distribution of HIF-1α in SGC-7901 cells, which might be one of the mechanisms of its chemosensitizing effect on cancer cells[3].
Cell Research Cell lines SGC-7901 cell line
Concentrations 20 μg/ml
Incubation Time 24 h
Method

Pantoprazole sodium salts are resuspended in normal saline (0.85%) at 5 mg/ml immediately prior to use. When the SGC-7901 cells have reached 60–70% confluence, PPZ is added at a final concentration of 20 µg/ml, and the cells are cultured for additional experiments. For example, The SGC-7901 cells are seeded in 100 µl of medium per well, at a density of 1×104/well, in 96-well plates and treated with PPZ for 24 h.
In Vivo
In vivo After PPZ treatment, apoptotic cell death is seen selectively in cancer cells and is accompanied with extracellular signal-regulated kinase deactivation. By contrast, normal gastric mucosal cells show the resistance to PPZ-induced apoptosis through the overexpression of antiapoptotic regulators including HSP70 and HSP27. In a xenograft model of nude mice, administration of PPZ significantly inhibits tumorigenesis and induces large-scale apoptosis of tumor cells[4].
Animal Research Animal Models Mice inoculated with MKN-45 cells (Xenograft Model of Nude Mice)
Dosages 0.4 mg/kg 
Administration intratumor injection 

Chemical Information & Solubility

Molecular Weight 405.35 Formula

C16H14F2N3NaO4S
CAS No. 138786-67-1 SDF Download Pantoprazole sodium SDF
Smiles COC1=C(C(=NC=C1)CS(=O)C2=NC3=C([N-]2)C=CC(=C3)OC(F)F)OC.[Na+]
Storage (From the date of receipt)

In vitro
Batch:

DMSO : 81 mg/mL ( (199.82 mM)； Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Water : 81 mg/mL

Ethanol : 81 mg/mL


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In vivo
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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
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Tech Support

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.

Handling Instructions

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