首页> 美国卫生研究院文献>Molecules >Design and Synthesis of Molecular Hybrids of Sophora Alkaloids and Cinnamic Acids as Potential Antitumor Agents
【2h】

Design and Synthesis of Molecular Hybrids of Sophora Alkaloids and Cinnamic Acids as Potential Antitumor Agents

机译:槐花生物碱和肉桂酸分子杂合物作为潜在抗肿瘤药物的设计与合成

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Twenty-five sophora alkaloids-cinnamic acid hybrids (including matrine-cinnamic acid hybrids, sophoridine-cinnamic acid hybrids, and sophocarpine-cinnamic acid hybrids) were designed, synthesized, and evaluated in vitro against three human tumor cell lines (HeLa, HepG2 and A549) with cisplatin as a positive control. Some matrine-cinnamic acid and sophoridine-cinnamic acid compounds exhibited potent effect against all three cancer cell lines, such as compounds , , , and . The structure-activity relationship study of the synthesized compounds was also performed. Preliminary mechanistic studies indicated that compounds and could induce apoptosis in HepG2 cell line. Further, compounds and altered mitochondrial membrane potential and produced ROS leading to cell apoptosis of HepG2 cells. Overall, our findings suggested that these compounds may provide promising lead compounds for further development as antitumor agents by structural modification.
机译:设计,合成了二十五个槐属生物碱-肉桂酸杂种(包括苦参碱-肉桂酸杂种,槐定啶-肉桂酸杂种和槐果皮-肉桂酸杂种),并在体外针对三种人类肿瘤细胞系(HeLa,HepG2和A549),以顺铂为阳性对照。某些苦参碱肉桂酸和槐定啶肉桂酸化合物对所有三种癌细胞系均显示出强效作用,例如化合物,,和。还进行了合成化合物的构效关系研究。初步的机理研究表明该化合物可诱导HepG2细胞凋亡。此外,化合物和线粒体膜电位改变并产生ROS,导致HepG2细胞凋亡。总体而言,我们的发现表明这些化合物可能通过结构修饰为抗肿瘤剂的进一步开发提供有前途的先导化合物。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号