张阳, 杨雨, 李家明, 马晓东, 张艳春, 王玉骏, 朱盼虎. 新型川芎嗪类衍生物的设计、合成及其生物活性的研究J. 药学学报, 2017,52(11): 1722-1730. doi: 10.16438/j.0513-4870.2017-0323
引用本文: 张阳, 杨雨, 李家明, 马晓东, 张艳春, 王玉骏, 朱盼虎. 新型川芎嗪类衍生物的设计、合成及其生物活性的研究J. 药学学报, 2017,52(11): 1722-1730. doi: 10.16438/j.0513-4870.2017-0323
ZHANG Yang, YANG Yu, LI Jia-ming, MA Xiao-dong, ZHANG Yan-chun, WANG Yu-jun, ZHU Pan-hu. Design, synthesis and biological evaluation of the novel ligustrazine derivatives J. Acta Pharmaceutica Sinica, 2017,52(11): 1722-1730. doi: 10.16438/j.0513-4870.2017-0323
Citation: ZHANG Yang, YANG Yu, LI Jia-ming, MA Xiao-dong, ZHANG Yan-chun, WANG Yu-jun, ZHU Pan-hu. Design, synthesis and biological evaluation of the novel ligustrazine derivatives J. Acta Pharmaceutica Sinica, 2017,52(11): 1722-1730. doi: 10.16438/j.0513-4870.2017-0323

新型川芎嗪类衍生物的设计、合成及其生物活性的研究

Design, synthesis and biological evaluation of the novel ligustrazine derivatives

  • 摘要: 以川芎嗪为先导化合物,设计合成了10个川芎嗪类衍生物,其结构经1H NMR、13C NMR、ESI-MS确证。采用MTT法考察目标化合物对A549、A549/DDP和HBE细胞株增殖的影响;采用划痕实验,transwell小室法考察目标化合物对A549迁移和侵袭能力的影响;采用Western印迹考察目标化合物对A549细胞迁移和侵袭的作用机制;另外,通过流式细胞仪分析其细胞周期。结果显示,目标化合物Z8Z10有一定的抗增殖活性,其对A549细胞迁移和侵袭的能力有很强的抑制作用;其抑制作用与MMP-2和MMP-9浓度水平下降有关。细胞周期分析显示,目标化合物Z8Z10会增强G2/M期细胞阻滞。

     

    Abstract: Using ligustrazine as the leading compound, we designed and synthesized ten novel ligustrazine derivatives, whose structures were determined by 1H NMR, 13C NMR and MS. Inhibitory effects of the new compounds on the proliferation of A549, A549/DDP and HBE cells were detected by MTT assay. The inhibi-tory activity of the synthesized compounds on migration and invasion of A549 cells were evaluated through scratch assay and transwell assay. Mechanism of the inhibition on migration and invasion was investigated by Western blotting. In addition, the cell cycle was analyzed with flow cytometry. The results showed that, both compounds Z8 and Z10 have an anti-proliferative activity, and the potencies of inhibition of tumor-cell migration and invasion were attributed to the down-regulation of MMP-2 and MMP-9. The compounds Z8 and Z10 could also enhance G2/M arrest in A549 cell as revealed by cell cycle analysis.

     

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