Design, synthesis, and characterization of oxadiazolopyrazine analogs with application as anticancer agents
作者:Wei‐Chia Chen、Chia‐Ling Chen、Tzu‐Ting Chang、Feng‐Chun Hsieh、Wei‐Sheng Chen、Wen‐Shan Li
DOI:10.1002/jccs.202100438
日期:2022.2
Here, we describe the synthesis and evaluation of a class of cell-permeable indeno-oxadiazolopyrazine analogs as the anticancer agents. A new and facile approach to the synthesis of substituted analogs of indeno-oxadiazolopyrazine is illustrated. We find that the designed indeno-oxadiazolopyrazines, 3, 4, 10, 11, 15, and 16, act as potent anticancer agents compared to camptothecin, topoisomerase I
在这里,我们描述了一类可渗透细胞的茚并恶二唑并吡嗪类似物作为抗癌剂的合成和评价。说明了合成茚并恶二唑并吡嗪的取代类似物的一种新的简便方法。我们发现设计的茚并恶二唑并吡嗪3、4、10、11、15和16,与拓扑异构酶 I 抑制剂喜树碱相比,可作为有效的抗癌剂。这些观察结果表明,在 A 环的 C-5、C-6 和 C-8 位置上的给电子基团(甲氧基)或在 C-6 和 C-7 位置上的吸电子基团(氟)对 MDA-MB-231、BT549 和 MCF7 细胞系的抗增殖活性需要茚并恶二唑并吡嗪。