Synthesis and Anticancer Activity Evaluation of Azepinobisindoles; the Isomeric Iheyamine A Derivatives
作者:Weerachai Phutdhawong、Sopita Rattanopas、Jitnapa Sirirak、Thongchai Taechowisan、Waya S. Phutdhawong
DOI:10.13005/ojc/350231
日期:2019.4.25
Azepinobisindole derivatives, the isomeric Iheyamine skeleton, were prepared and their anticancer activity evaluation were investigated against two human cancer cell lines, Hepatocellular carcinoma (HepG2) and human cervical cancer line (HeLa) as well as the normal cell line (Vero cell line) using MTT assay. The anticancer activity results indicated that 2-methoxy-5-methyl5H-azepino[2,3-b:4,5-b]diindole
制备了异戊二烯异构体骨架-Azepinobisindole衍生物,并使用它们对两种人类癌细胞系,肝细胞癌(HepG2)和人宫颈癌系(HeLa)以及正常细胞系(Vero细胞系)进行了抗癌活性评估MTT测定。抗癌活性结果表明,2-甲氧基-5-甲基5H-氮杂环庚烷[2,3-b:4,5-b]二吲哚是针对所测试细胞系最具活性的衍生物。另外,在计算机上进行的分子对接研究在计算机上对氮杂环庚烷吲哚对细胞周期蛋白依赖性激酶2(CDK2)的抑制作用表明,所有合成的化合物都很好地适合CDK2的结合腔。关键词:阿斯皮诺双吲哚异美托体胺抗癌活性CDK2分子对接。