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一种新型[1,2,4]三唑并[1,5-a]嘧啶基苯连接甾体二聚体:合成及其细胞毒性活性。

A novel [1,2,4] triazolo [1,5-a] pyrimidine-based phenyl-linked steroid dimer: synthesis and its cytotoxic activity.

机构信息

School of Pharmaceutical Sciences and New Drug Research & Development Center, Zhengzhou University, Zhengzhou 450001, PR China.

出版信息

Eur J Med Chem. 2013 Nov;69:323-30. doi: 10.1016/j.ejmech.2013.08.029. Epub 2013 Sep 4.

Abstract

A novel [1,2,4] triazolo [1,5-a] pyrimidine-based phenyl-linked steroid dimer was designed, synthesized and evaluated for its cytotoxic activity against five human cancer cell lines and the cytotoxicity against human normal liver cell L-02. Compound 3 showed excellent cytotoxic activity and good selectivity between cancer and normal cells. Further mechanistic studies revealed that treatment of EC109 cells with compound 3 caused an obvious G2/M arrest in a concentration- and time-dependent manner and induced apoptosis probably through the mitochondrial pathway accompanied with the decrease of mitochondrial membrane potential, activations of caspase-9/-3, cleavage of MDM2 as well as up-regulation of the expressions of p53 and Bax.

摘要

设计、合成了一种新型[1,2,4]三唑并[1,5-a]嘧啶基苯连接甾体二聚体,并评价了其对五种人癌细胞系的细胞毒性活性以及对人正常肝细胞 L-02 的细胞毒性。化合物 3 表现出优异的细胞毒性活性和良好的癌细胞与正常细胞之间的选择性。进一步的机制研究表明,化合物 3 处理 EC109 细胞会导致明显的 G2/M 期阻滞,呈浓度和时间依赖性,并通过线粒体途径诱导细胞凋亡,伴随着线粒体膜电位的降低、caspase-9/-3 的激活、MDM2 的切割以及 p53 和 Bax 的表达上调。

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