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含苯基的氨基脲衍生物:合成、抗癌活性、细胞周期、诱导凋亡及代谢稳定性研究

Semicarbazone Derivatives Bearing Phenyl Moiety: Synthesis, Anticancer Activity, Cell Cycle, Apoptosis-Inducing and Metabolic Stability Study.

作者信息

Ma Junjie, Ni Xin, Gao Yali, Huang Kun, Wang Yu, Liu Jiaan, Gong Guowei

机构信息

Medical College, Huaqiao University.

Pharmacy Department, the Second Affiliated Hospital of Fujian Medical University.

出版信息

Chem Pharm Bull (Tokyo). 2019 Apr 1;67(4):351-360. doi: 10.1248/cpb.c18-00738. Epub 2019 Jan 24.

Abstract

A series of semicarbazone derivatives bearing phenyl moiety were synthesized and evaluated for the vitro anticancer activities in four human cancer cell lines (human colon cancer (HT29), human neuro-blastoma (SK-N-SH), human breast cancer (MDA-MB-231), and human gastric cancer (MKN45)). Biological evaluation led to the identification of 11q and 11s, which showed excellent anticancer activities against tested cancer cell lines with IC values ranging from 0.32 to 1.57 µM, respectively, while exhibiting weak cytotoxicity on the normal cells (human umbilical vein endothelial cell (HUVEC)). Flow cytometric assay for cell cycle and apoptosis revealed that 11q and 11s caused an arrest in the Sub-G1 cell cycle and inhibited proliferation of cancer cells by inducing apoptosis in a dose-dependent manner. Further enzymatic assay suggested that 11q and 11s could significantly activated procaspase-3 to caspase-3. Metabolic stability study indicated that 11q and 11s showed moderate stability in vitro in human and rat liver microsomes. In view of promising pharmacological activities of 11q and 11s, which had emerged as the valuable lead for further development in the treatment for cancer.

摘要

合成了一系列带有苯基部分的氨基脲衍生物,并在四种人类癌细胞系(人结肠癌(HT29)、人神经母细胞瘤(SK-N-SH)、人乳腺癌(MDA-MB-231)和人胃癌(MKN45))中评估了它们的体外抗癌活性。生物学评估鉴定出了11q和11s,它们对测试的癌细胞系显示出优异的抗癌活性,IC值分别为0.32至1.57 μM,同时对正常细胞(人脐静脉内皮细胞(HUVEC))表现出较弱的细胞毒性。细胞周期和凋亡的流式细胞术分析表明,11q和11s导致亚G1期细胞周期停滞,并通过以剂量依赖性方式诱导凋亡来抑制癌细胞的增殖。进一步的酶活性测定表明,11q和11s可将procaspase-3显著激活为caspase-3。代谢稳定性研究表明,11q和11s在人和大鼠肝微粒体中的体外稳定性适中。鉴于11q和11s具有良好的药理活性,它们已成为癌症治疗进一步发展的有价值先导物。

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