兰索拉唑
药代动力学
化学
药理学
口服
CYP3A4型
代谢物
活性代谢物
尿
细胞色素P450
曲线下面积
医学
酶
生物化学
奥美拉唑
作者
B. Delhotal Landes,J P Petite,B Flouvat
标识
DOI:10.2165/00003088-199528060-00004
摘要
Lansoprazole, a benzimidazole derivative with antisecretory and antiulcer activities, inhibits the acid pump activity at the final stage of the enzyme process and therefore reduces the acid secretion of parietal cells. Lansoprazole is converted to active metabolites in the acid environment of these cells. It is rapidly absorbed from a gastric acid-resistant formulation and is approximately 97% bound in human plasma.
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