目的设计合成新型苯胺类苯并咪唑衍生物，并评价其对大白鼠胃液分泌和胃酸分泌的作用。
Aim to design and synthesize the novel aniline-type derivatives of benzimidazole, and to assay their activities of inhibiting secretion of gastric juice and gastric acids.
苯胺类硝基衍生物和苯酚的硝基衍生物分子中存在分子内氢键。
For nitro derivatives of aminobenzenes and phenols, there is intermolecular Hydrogen bond in the molecule.
在结构与活性的关系资讯中显示， 7-苯基-6-氮基吲哚-1-磺胺类衍生物的活性比7-苯胺基-6-氮基吲哚-1-磺胺类衍 生物的活性好。
Structure- activity relationship information revealed that 7-aryl-6- azaindole-1- sulfonamide derivatives was more potent than 7-anilino-6-azaindole-1- sulfonamide derivatives.
在结构与活性的关系资讯中显示， 7-苯基-6-氮基吲哚-1-磺胺类衍生物的活性比7-苯胺基-6-氮基吲哚-1-磺胺类衍 生物的活性好。
Structure- activity relationship information revealed that 7-aryl-6- azaindole-1- sulfonamide derivatives was more potent than 7-anilino-6-azaindole-1- sulfonamide derivatives.
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