首页> 外文期刊>Pharmacological reports: PR >Natural and synthetic acridines/acridones as antitumor agents: their biological activities and methods of synthesis.
【24h】

Natural and synthetic acridines/acridones as antitumor agents: their biological activities and methods of synthesis.

机译:天然和合成a啶/ ac啶酮作为抗肿瘤剂:它们的生物学活性和合成方法。

获取原文
           

摘要

Acridine derivatives constitute a class of compounds that are being intensively studied as potential anticancer drugs. Acridines are well-known for their high cytotoxic activity; however, their clinical application is limited or even excluded because of side effects. Numerous synthetic methods are focused on the preparation of target acridine skeletons or modifications of naturally occurring compounds, such as acridone alkaloids, that exhibit promising anticancer activities. They have been examined in vitro and in vivo to test their importance for cancer treatment and to establish the mechanism of action at both the molecular and cellular level, which is necessary for the optimization of their properties so that they are suitable in chemotherapy. In this article, we review natural and synthetic acridine/acridone analogs, their application as anticancer drugs and methods for their preparation
机译:cr啶衍生物构成一类化合物,正在作为潜在的抗癌药物进行深入研究。 cr啶因其高细胞毒性活性而闻名。然而,由于副作用,它们的临床应用受到限制甚至被排除在外。许多合成方法集中于目标target啶骨架的制备或天然化合物(如a啶酮生物碱)的修饰,这些化合物显示出有希望的抗癌活性。已在体外和体内对它们进行了检查,以测试它们在癌症治疗中的重要性,并在分子和细胞水平上建立作用机制,这对于优化其性能至关重要,因此它们适用于化学疗法。在本文中,我们综述了天然和合成的cr啶/ ac啶酮类似物,其作为抗癌药的应用及其制备方法

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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