Synthesis and hypoglycemic activity of some substituted 2-arylthiazolo[3.2-a]pyridinium salts
作者:Benjamin Blank、Nicholas W. DiTullio、Arnold J. Krog、Harry J. Saunders
DOI:10.1021/jm00203a019
日期:1978.5
A series of substituted 2-arylthiazolo[3,2-a]pyridinium salts (1a-q) was prepared by known methods and tested for hypoglycemic activity in 48-h fasted rats. Two compounds, 2-phenylthiazolo- and 8-methyl-2-phenythiazolo[3,2-a]pyridinium perchlorate (1a and 1q), showed consistent hypoglycemic activity in this screen, demonstrating that a high degree of structural specificity was required for hypoglycemic
通过已知方法制备一系列取代的2-芳基噻唑并[3,2-a]吡啶鎓盐(1a-q),并在禁食48小时的大鼠中测试其降血糖活性。两种化合物,即2-苯基噻唑-和8-甲基-2-吩噻唑[3,2-a]吡啶鎓高氯酸(1a和1q)在此筛选中显示出一致的降血糖活性,表明降血糖需要高度的结构特异性活动。在较高剂量下,1a和1q的降血糖活性与肝甘油三酸酯水平升高有关。