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Famotidine(MK-208)是新的高效的组织胺H_2受体拮抗剂,是一种脒噻唑(guanylt-hiazole)的衍生物,其化学结构与含咪唑环(imidazole)的甲氰咪胍以及含呋喃环(furane)的雷尼替丁不同.药理特性动物实验及临床实验研究表明其有如下药理特性:1.Famotidine经口服吸收后能很好地抑制基础胃酸分泌、夜间胃酸分泌、五肽胃泌素及试验餐引起的胃酸分泌.对胃酸的抑制作
Famotidine (MK-208) is a new and highly effective histamine H 2 receptor antagonist. It is a derivative of guanylt-hiazole with chemical structure similar to that of imidazole with cimetidine and Furan ranitidine pharmacological properties of animal experiments and clinical studies have shown that the following pharmacological properties: 1.Famotidine oral absorption can be a good basis to inhibit basal gastric acid secretion, gastric acid secretion at night, pentapeptide stomach Gastrin and test meal caused by gastric acid secretion. Inhibition of gastric acid