Tegoprazan
Tegoprazan
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Tegoprazan

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Catalog Number PR942195553
CAS 942195-55-3
Synonyms CJ-12420; RQ-00000004
Molecular Weight 387.38
Molecular Formula C20H19F2N3O3
Purity >99%
Color Off-white to light yellow
Drug Categories Alimentary Tract and Metabolism; Drugs for Acid Related Disorders; Drugs for Peptic Ulcer and Gastro-Oesophageal Reflux Disease (Gord); Gastric Acid Lowering Agents; Proton Pump Inhibitors
Drug Interactions Alendronic acid-The therapeutic efficacy of Alendronic acid can be decreased when used in combination with Tegoprazan.
Amphetamine-Tegoprazan can cause an increase in the absorption of Amphetamine resulting in an increased serum concentration and potentially a worsening of adverse effects.
Amprenavir-Tegoprazan can cause a decrease in the absorption of Amprenavir resulting in a reduced serum concentration and potentially a decrease in efficacy.
Asunaprevir-Tegoprazan can cause a decrease in the absorption of Asunaprevir resulting in a reduced serum concentration and potentially a decrease in efficacy.
Atazanavir-Tegoprazan can cause a decrease in the absorption of Atazanavir resulting in a reduced serum concentration and potentially a decrease in efficacy.
Physical State Solid
Type Small Molecule
Pharmacology

Mechanism of Action

Tegoprazan operates as a highly selective and potent potassium-competitive acid blocker, distinguishing itself from traditional proton-pump inhibitors through its unique mechanism of action. Unlike proton-pump inhibitors, Tegoprazan does not necessitate conversion into an active form. It directly targets and reversibly inhibits the H+/K+-ATPase enzyme in a potassium-competitive manner. This efficacy is attributed to Tegoprazan's properties as an acid-resistant weak base, which allows it to persist effectively in the highly acidic environment of gastric parietal cell canaliculi.

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