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SCH28080

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Catalog No. T16865Cas No. 76081-98-6

SCH28080 is a reversible and K+-competitive inhibitor of gastric H+/K+-ATPase with an IC50 value of 20 nM (rabbit microsomal membrane).SCH28080 is a potent inhibitor of acid secretion in vivo with anti-ulcer activity, anti-secretory and cytoprotective activity.

SCH28080

SCH28080

🥰Excellent
Purity: 97.12%
Catalog No. T16865Cas No. 76081-98-6
SCH28080 is a reversible and K+-competitive inhibitor of gastric H+/K+-ATPase with an IC50 value of 20 nM (rabbit microsomal membrane).SCH28080 is a potent inhibitor of acid secretion in vivo with anti-ulcer activity, anti-secretory and cytoprotective activity.
Pack SizePriceAvailabilityQuantity
1 mg$31In Stock
5 mg$81In Stock
10 mg$139In Stock
25 mg$279In Stock
50 mg$416In Stock
100 mg$593In Stock
1 mL x 10 mM (in DMSO)$79In Stock
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Purity:97.12%
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Product Introduction

Bioactivity
Description
SCH28080 is a reversible and K+-competitive inhibitor of gastric H+/K+-ATPase with an IC50 value of 20 nM (rabbit microsomal membrane).SCH28080 is a potent inhibitor of acid secretion in vivo with anti-ulcer activity, anti-secretory and cytoprotective activity.
Targets&IC50
H+, K+-ATPase:0.12 μM(Ki), Aminopyrine:0.029 μM, INS-1E cells:22.9 µM, INS-1E cells:15.3 µM, H+, K+-ATPase, rabbit microsomal membranes:20 nM
In vitro
SCH28080 competitively hinders ATP hydrolysis stimulated by K+, with a Ki value of 0.12 μM.[1]
SCH28080 effectively suppresses histamine-induced uptake of [14C]aminopyrine in isolated rabbit parietal cells, demonstrating an IC50 of 0.029 μM.[1]
SCH28080 elicits a dose-dependent decrease in cell viability, with IC50 values of 22.9 µM and 15.3 µM following 2-hour and 24-hour treatments, respectively. And at concentration of 100 µM, cell viability drops below 10% as early as 2 hours.[2]
SCH28080 induces apoptosis and exhibits cytotoxicity at higher doses.[2].
SCH28080 also impedes insulin secretion by activating IK ATP and inhibiting L-type voltage-gated Ca2+ channels, ultimately reducing cell viability and induces apoptosis/necrosis in a dose-dependent manner.[2]
In vivo
SCH28080 (20 mg/kg; i.p.) effectively reduces gastric ulcers induced by pylorus ligation in rats.[3]
Chemical Properties
Molecular Weight277.32
FormulaC17H15N3O
Cas No.76081-98-6
SmilesCc1nc2c(OCc3ccccc3)cccn2c1CC#N
Relative Density.1.16g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 90.0 mg/mL (324.5 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.6059 mL18.0297 mL36.0594 mL180.2971 mL
5 mM0.7212 mL3.6059 mL7.2119 mL36.0594 mL
10 mM0.3606 mL1.8030 mL3.6059 mL18.0297 mL
20 mM0.1803 mL0.9015 mL1.8030 mL9.0149 mL
50 mM0.0721 mL0.3606 mL0.7212 mL3.6059 mL
100 mM0.0361 mL0.1803 mL0.3606 mL1.8030 mL

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Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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