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苯并噻唑连接的苯并嘧啶并二酮及其二酮的合成及抗癌潜力作为线粒体凋亡诱导剂。

Synthesis and anticancer potential of benzothiazole linked phenylpyridopyrimidinones and their diones as mitochondrial apoptotic inducers.

机构信息

Medicinal Chemistry and Pharmacology, CSIR-Indian Institute of Chemical Technology, Tarnaka, Hyderabad 500 007, India.

Medicinal Chemistry and Pharmacology, CSIR-Indian Institute of Chemical Technology, Tarnaka, Hyderabad 500 007, India.

出版信息

Bioorg Med Chem Lett. 2014 Jan 1;24(1):147-51. doi: 10.1016/j.bmcl.2013.11.057. Epub 2013 Dec 1.

Abstract

A series of benzothiazole linked phenylpyridopyrimidinones (8a-g) and their diones (9a-g) have been designed, synthesized and evaluated for their anticancer activity. Among the series one of the conjugate 8b showed significant cytotoxicity against human cervical cancer cell line ME-180 with IC50 value of 4.01μM. This compound was tested on the cell cycle perturbations and DNA damage. Flow cytometry analysis revealed that the compound 8b showed drastic cell cycle perturbations due to concentration dependent increase in the sub-G0 phase in ME-180 cell line. DNA fragmentation and Hoechst staining reveals that this compound induced cell death by apoptosis. Further caspase-3 and loss of mitochondrial membrane potential suggested that the compound induces cell death by apoptosis.

摘要

一系列苯并噻唑连接的苯基吡啶并嘧啶酮(8a-g)及其二酮(9a-g)已经被设计、合成并评估了它们的抗癌活性。在该系列中,一种共轭物 8b 对人宫颈癌 ME-180 细胞系表现出显著的细胞毒性,IC50 值为 4.01μM。该化合物在细胞周期扰动和 DNA 损伤方面进行了测试。流式细胞术分析显示,该化合物 8b 由于在 ME-180 细胞系中浓度依赖性地增加亚 G0 期而导致明显的细胞周期扰动。DNA 片段化和 Hoechst 染色显示,该化合物通过细胞凋亡诱导细胞死亡。进一步的 caspase-3 和线粒体膜电位丧失表明,该化合物通过细胞凋亡诱导细胞死亡。

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