ChemicalBook--->CAS DataBase List--->1902954-87-3

1902954-87-3

1902954-87-3 Structure

1902954-87-3 Structure
IdentificationBack Directory
[Name]

DWP14012 hydrochloride
[CAS]

1902954-87-3
[Synonyms]

DWP14012 hydrochloride
Abeprazan hydrochloride
[Molecular Formula]

C19H18ClF3N2O3S
[MDL Number]

MFCD34469942
[MOL File]

1902954-87-3.mol
[Molecular Weight]

446.87
Chemical PropertiesBack Directory
[storage temp. ]

-20°C, away from moisture
[form ]

Solid
[color ]

White to light yellow
Hazard InformationBack Directory
[Uses]

Abeprazan hydrochloride (DWP14012 hydrochloride) is a potassium-competitive acid blocker. Abeprazan hydrochloride inhibits H+, K+- ATPase by reversible potassium-competitive ionic binding with no acid activation required. Abeprazan hydrochloride is developed as a potential alternative to proton pump inhibitor for the treatment of acid-related diseases[1].
[Biological Activity]

Abeprazan hydrochloride (DWP14012 hydrochloride) is a potassium-competitive acid blocker. Abeprazan hydrochloride inhibits H+, K+- ATPase by reversible potassium-competitive ionic binding with no acid activation required. Abeprazan hydrochloride is developed as a potential alternative to proton pump inhibitor for the treatment of acid-related diseases[1]. The mechanism of action of Abeprazan hydrochloride is reversibly binding to H+, K+‐ATPase, and, unlike that of PPIs, does not require acidic environment for drug activation[1]. Abeprazan hydrochloride (DWP14012 hydrochloride) inhibits acid secretion in a dose-dependent manner and the inhibition of gastric acid secretion is equal to or greater than that of vonoprazan, a previously approved P-CAB, in various in vivo studies using pylorus-ligated rats, lumen-perfused rat models and heidenhain pouch dog models[1].
[in vivo]

Abeprazan hydrochloride (DWP14012 hydrochloride) inhibits acid secretion in a dose-dependent manner and the inhibition of gastric acid secretion is equal to or greater than that of vonoprazan, a previously approved P-CAB, in various in vivo studies using pylorus-ligated rats, lumen-perfused rat models and heidenhain pouch dog models[1].

[storage]

-20°C, away from moisture
[References]

[1]. Sunwoo J, et al. Safety, tolerability, pharmacodynamics and pharmacokinetics of DWP14012, a novel potassium-competitive acid blocker, in healthy male subjects. Aliment Pharmacol Ther. 2018 Jul;48(2):206-218.
Spectrum DetailBack Directory
[Spectrum Detail]

DWP14012 hydrochloride(1902954-87-3)1HNMR
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