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Tegoprazan

Chemical Structure : Tegoprazan

CAS No.: 942195-55-3

Tegoprazan (CJ 12420, RQ-00000004, RQ-4)

Catalog No.: PC-60811Not For Human Use, Lab Use Only.

Tegoprazan (CJ 12420, RQ-00000004, RQ-4) is a novel potent, highly selective, competitive and orally active inhibitor of gastric H+/K+-ATPase with IC50 of ranging 0.29-0.52 uM porcine, canine and human H+/K+-ATPases in vitro.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

Tegoprazan (CJ 12420, RQ-00000004, RQ-4) is a novel potent, highly selective, competitive and orally active inhibitor of gastric H+/K+-ATPase with IC50 of ranging 0.29-0.52 uM porcine, canine and human H+/K+-ATPases in vitro.
Tegoprazan displays no activity against canine kidney Na+/K+-ATPase (IC50>100 uM).
Tegoprazan potently inhibits histamine-induced gastric acid secretion in dogs and a complete inhibition at 1.0 mg/kg starting from 1 hr after administration, reverses the pentagastrin-induced acidified gastric pH to the neutral range at 1-3 mg/kg, immediately evoks a gastric phase III contraction of migrating motor complex (MMC) in pentagastrin-treated dogs.

Physicochemical Properties

M.Wt 387.387
Formula C20H19F2N3O3
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

(S)-4-((5,7-difluorochroman-4-yl)oxy)-N,N,2-trimethyl-1H-benzo[d]imidazole-6-carboxamide

References

1. Takahashi N, et al. J Pharmacol Exp Ther. 2017 Nov 27. pii: jpet.117.244202.

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