Green Synthesis, Characterization and Antidiabetic Activity of 2-Substituted Aryl/Alkyl-N-Aryl/Alkyl Imidazo[1,2-a]pyridin-3-amine Derivatives
作者:Tata Veereswara Rao Kota、Hima Bindu Gandham、Paul Douglas Sanasi
DOI:10.14233/ajchem.2018.21220
日期:——
appealing benefits they offer. Imidazole fused polyheterocycles containing ring junction nitrogen have attracted considerable interest in medicinal chemistry in view of their uses as anti-inflammatory [2], anticancer [3], antibacterial [4] and antituberculosis [5] agents. The importance of imidazo[1,2-a]pyridine is evident from the fact that it is prevalent in several marketed drugs such as olprinone
在氮衍生物中,咪唑稠合杂环在药物和有机化学中变得越来越重要,因为它们表现出广泛的药理和生物活性,如抗病毒、抗菌、抗真菌和抗炎特性[1]。咪唑并吡啶支架在药物发现领域的重要性因其提供的吸引人的好处而广为人知。鉴于其作为抗炎剂 [2]、抗癌剂 [3]、抗菌剂 [4] 和抗结核剂 [5] 的用途,含有环连接氮的咪唑稠合多杂环化合物在药物化学中引起了相当大的兴趣。咪唑并[1,2-a]吡啶的重要性显而易见,因为它在几种市售药物中普遍存在,例如olprinone(强心剂,一种磷酸二酯酶-PDE 3 抑制剂)[6,7]、唑吡坦(催眠药)[8]、左旋咪唑(抗癌药)[9,10]、阿吡坦(一种非镇静抗焦虑药)[11-13]、唑利胺(抗炎药)[ 14,15]。由于它们的结构特征 [16-18]、镇静剂(saripidem 和 necopidem)[19,20],它们也用于分子识别和生物成像探针。衍生自咪唑并[1