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H~+/K~+-ATP酶抑制剂苯并咪唑类衍生物的研究
Studies on H\++/K\++ATPase Inhibitors Benzimidazole Derivatives
【摘要】 H+/K+ATP酶是胃酸分泌的最后环节,在合成H+/K+ATP酶抑制剂泮托拉唑的基础上,设计合成了12个未见文献报道的苯并咪唑类衍生物,经红外光谱、核磁共振氢谱和元素分析确定了结构.初步药理筛选实验表明:化合物(5b),(6b),(6d)具有抑制胃酸分泌的作用,其中化合物(6d)作用最强.
【Abstract】 H\++/K\++ATPase is the last passageway of gastric acid secretion.On the basis of synthesis of the H\++/K\++ATPase inhibitor pantoprazole,twelve benzimidazole derivatives were synthesized for the first time,and their structures were proved by IR,\+1HNMR and elementary analysis.Their antisecretory activities were evaluated in vivo,the compounds (5b),(6b) and (6d) have antisecretory activities and compound (6d) was the most potent.
【关键词】 H~+/K~+-ATP酶抑制剂;
苯并咪唑类衍生物;
抑制胃酸分泌;
【Key words】 H\++/K\++ATPase inhibitors; benzimidazole derivatives; inhibiting gastric acid secretion;
【Key words】 H\++/K\++ATPase inhibitors; benzimidazole derivatives; inhibiting gastric acid secretion;
- 【文献出处】 中国药物化学杂志 ,CHINESE JOURNAL OF MEDICINAL CHEMISTRY , 编辑部邮箱 ,1999年02期
- 【分类号】R914
- 【被引频次】16
- 【下载频次】167