Synthesis and pharmacological activity of imidazo[4,5-c]pyridine derivatives
作者:O. M. Glozman、É. K. Orlova、L. M. Meshcheryakova、T. A. Voronina、T. L. Garibova、N. V. Markina、L. D. Smirnov
DOI:10.1007/bf00766375
日期:1989.8
Derivatives of imidazo[4,5-c]pyridlne (IP) show a variety of pharmacological activities [3, 9]. In particular, there are IP derivatives active as GABAergir agonists and selective anxiolytic antagonists [2, 8]. To investigate the neurotropic activity of IP derivatives, four compounds (la-d) were prepared with adamantyl, dipropylmethyl, 4-chlorophenoxymethyl, and pyridyl-3-oxymethyl moieties as the pharmacophore
咪唑并 [4,5-c] 吡啶 (IP) 的衍生物显示出多种药理活性 [3, 9]。特别是,有作为 GABAergir 激动剂和选择性抗焦虑拮抗剂的 IP 衍生物 [2, 8]。为了研究 IP 衍生物的神经活性,制备了四种化合物 (la-d),其中金刚烷基、二丙基甲基、4-氯苯氧基甲基和吡啶基-3-氧基甲基部分作为 IP 位置 2 的药效基团。