化学
降级(电信)
水解
强制降级
碱性水解
色谱法
气相色谱-质谱法
ATP酶
钾
质谱法
核化学
酶
有机化学
计算机科学
电信
甲酸铵
作者
Kaijing Guo,Xiao He,Hóngyi Zhào,Chen Ma
标识
DOI:10.1016/j.jpba.2023.115323
摘要
Tegoprazan is a novel orally active potassium-competitive acid blocker (P-CAB), capable of binding to the K+ binding site of H+/K+-ATPase in a reversible way to inhibit gastric acid secretion. Tegoprazan has been approved for treating acid-related diseases. In this study, stress testings of tegoprazan were performed under various conditions, including hydrolysis (acidic, alkaline, and neutral), oxidation, photolysis, and thermal stress. Tegoprazan showed instability in acidic, alkaline, and oxidative conditions. Eight degradation products (DPs) were identified. The DPs were characterized by LC-HRMS, LC-MSn, or GC-Q-TOF-MS. Meanwhile, DP-1, DP-2 and DP-3 were successfully synthesized and confirmed by NMR. The degradation pathway of tegoprazan was summarized. To the best of our knowledge, this is the first study on the forced degradation of tegoprazan.
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