Linaprazan (AZD0865) inhibits gastric H+,K+-ATPase by K+-competitive binding. (IC50: 1.0 ± 0.2 μM)
It is a acid-suppressing agents with rapid onset of action and potent acid inhibition.
In vitro: Linaprazan can inhibit the final step in acid secretion. Linaprazanreduced porcine renal Na+,K+-ATPase activity by 9 ± 2%, demonstrating a high selectivity for H+,K+-ATPase.
In vivo: The reference for animal administration is 0.5-1.0 mg/kg. The greater degree of acid suppression with the 75-mg dose of Linaprazan would translate to a healing rate of 89% at 4 weeks.
分子式
C21H26N4O2
分子量
366.46
CAS号
248919-64-4
中文名称
利那拉生
运输条件
Room temperature in continental US; may vary elsewhere.