6-Aryl-4H-s-triazolo[4,3-a][1,4]benzodiazepines. Influence of 1-substitution on pharmacological activity
作者:Jackson B. Hester、Philip Von Voigtlander
DOI:10.1021/jm00197a021
日期:1979.11
series of 1-substituted 6-aryl-4H-s-triazolo[4,3-a][1,4]benzodiazepines was prepared and evaluated for central nervous system activity. It was found that electronegative substituents, such as trifluoromethyl, were detrimental to activity in this series. On the other hand, many compounds with electron-donating substituents at C-1 had interesting activity. In addition to showing anxiolytic potential
制备一系列1-取代的6-芳基-4H-s-三唑并[4,3-a] [1,4]苯并二氮杂并评估中枢神经系统活性。发现负电取代基,例如三氟甲基,对该系列的活性有害。另一方面,许多在C-1上带有给电子取代基的化合物具有令人感兴趣的活性。除了表现出抗焦虑的潜力外,有些还活跃于检测抗抑郁和抗精神病活性的试验中。在C-1具有4-甲基-1-哌嗪基和4-吗啉基取代基的几种类似物是特别令人感兴趣的。