程新越, 唐胜, 孔兰英, 李玉环, 宋丹青. 12-N-苯磺酰苦参醚衍生物的合成及其抗柯萨奇病毒B3活性研究J. 药学学报, 2016,51(4): 606-612. doi: 10.16438/j.0513-4870.2015-1011
引用本文: 程新越, 唐胜, 孔兰英, 李玉环, 宋丹青. 12-N-苯磺酰苦参醚衍生物的合成及其抗柯萨奇病毒B3活性研究J. 药学学报, 2016,51(4): 606-612. doi: 10.16438/j.0513-4870.2015-1011
CHENG Xin-yue, TANG Sheng, KONG Lan-ying, LI Yu-huan, SONG Dan-qing. Synthesis and biological evaluation of 12-N-benzenesulfonyl matrinic ether derivatives as anti-coxsackievirus B3 agentsJ. Acta Pharmaceutica Sinica, 2016,51(4): 606-612. doi: 10.16438/j.0513-4870.2015-1011
Citation: CHENG Xin-yue, TANG Sheng, KONG Lan-ying, LI Yu-huan, SONG Dan-qing. Synthesis and biological evaluation of 12-N-benzenesulfonyl matrinic ether derivatives as anti-coxsackievirus B3 agentsJ. Acta Pharmaceutica Sinica, 2016,51(4): 606-612. doi: 10.16438/j.0513-4870.2015-1011

12-N-苯磺酰苦参醚衍生物的合成及其抗柯萨奇病毒B3活性研究

Synthesis and biological evaluation of 12-N-benzenesulfonyl matrinic ether derivatives as anti-coxsackievirus B3 agents

  • 摘要: 12-N-m-氰基苯磺酰苦参丁甲醚是一个具有良好抗柯萨奇病毒B3(CVB3)活性的全新结构骨架化合物,本研究以其为先导物,共设计合成了15个全新结构的苦参醚衍生物。采用细胞病变效应(CPE)方法评价了其体外抗CVB3活性和细胞毒性。构效关系表明, 11-位碳链长度的缩短不利于活性提高。其中化合物c1显示出良好的抗CVB3活性, IC50值为7.1 μmol·L-1(SI为35.5),与先导物相当。构效关系结果为此类化合物的进一步结构优化提供了有益的信息。

     

    Abstract: 12-N-m-Cyanobenzenesulfonyl matrinic butyl methyl ether is a potent anti-coxsackievirus B3(CVB3) agent bearing a novel structure skeleton. Taking this compound as a lead, totally 15 novel target compounds have been synthesized and evaluated for the anti-CVB3 activities using CPE method. Structureactivity relationship (SAR) demonstrated that the shorten-length of 11-side chain was not helpful for keeping the good anti-virus activity. Among the newly synthesized compounds, compound c1 displayed a good anti-CVB3 activity with the IC50 of 7.1 μmol·L-1 and SI of 35.5, similar to that of the lead. The SAR results provided useful information for further optimization of these compounds in the molecular structure.

     

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