研究论文

新型吡唑酰基脲类化合物的设计合成、杀菌活性与分子对接研究

  • 孙娜波 ,
  • 沈钟华 ,
  • 翟志文 ,
  • 武宏科 ,
  • 翁建全 ,
  • 谭成侠 ,
  • 刘幸海
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  • a 浙江树人大学生物与环境学院 杭州 310015;
    b 浙江工业大学化学工程学院 杭州 310014

收稿日期: 2017-02-03

  修回日期: 2017-03-30

  网络出版日期: 2017-04-18

基金资助

国家自然科学基金(No.31401691)和浙江省自然科学基金(No.LY16C14007)资助项目.

Design, Synthesis, Fungicidal Activity and Docking Study of Acyl Urea Derivatives Containing Pyrazole Moiety

  • Sun Nabo ,
  • Shen Zhonghu ,
  • Zhai Zhiwen ,
  • Wu Hongke ,
  • Weng Jianquan ,
  • Tan Chengxia ,
  • Liu Xinghai
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  • a College of Biology and Environmental Engineering, Zhejiang Shuren University, Hangzhou 310015;
    b College of Chemical Engineering, Zhejiang University of Technology, Hangzhou 310014

Received date: 2017-02-03

  Revised date: 2017-03-30

  Online published: 2017-04-18

Supported by

Project supported by the National Natural Science Foundation of China (No. 31401691) and the Zhejiang Provincial Natural Science Foundation of China (No. LY16C14007).

摘要

以乙酰乙酸乙酯、原甲酸三乙酯、甲基肼等为原料,通过多步反应制备了一系列含吡唑的酰基脲类化合物.产物结构均经过1H NMR和HRMS确证;对所有化合物进行了杀菌活性测试,结果表明部分化合物对花生褐斑病菌、苹果轮纹病菌、水稻纹枯病菌、油菜菌核病菌具有较好的抑制效果,同时将高活性化合物7i与琥珀酸脱氢酶进行了对接,计算结果显示化合物7i能与琥珀酸脱氢酶形成稳定的复合物,化合物中的酰胺键能与酶中Ser39残基形成氢键作用.

本文引用格式

孙娜波 , 沈钟华 , 翟志文 , 武宏科 , 翁建全 , 谭成侠 , 刘幸海 . 新型吡唑酰基脲类化合物的设计合成、杀菌活性与分子对接研究[J]. 有机化学, 2017 , 37(8) : 2044 -2049 . DOI: 10.6023/cjoc201702003

Abstract

A series of novel acyl urea derivatives containing pyrazole moiety were synthesized from ethyl acetoacetate, triethyl orthoformate, methylhydrazine by multi-step reactions. Their structures were characterized by 1H NMR and HRMS spectra. The target compounds were evaluated for their fungicidal activity. The results indicated that some of the title compounds displayed certain fungicidal activities against Cercospora arachidicola, Sclerotinia sclerotiorum, Rhizoctonia solani and Physalopora piricola. The docking results indicated the hydrogen bond formed between the amide group and Ser 39 residue.

参考文献

[1] Russell, P. E. Outlooks Pest Manage. 2009, 20, 122.
[2] Mu, J. X.; Shi, Y. X.; Yang, M. Y.; Sun, Z. H.; Liu, X. H.; Li, B. J.; Sun, N. B. Molecules 2016, 21, 68.
[3] Elebe, H.; Rieck, H.; Dunkel, R. WO 02008195, 2002[Chem. Abstr. 2002, 136, 151162].
[4] Elebe, H.; Rieck, H.; Dunkel, R. WO 03010149, 2003[Chem. Abstr. 2003, 138, 137308].
[5] Du, S.; Tian, Z.; Yang, D.; Li, X.; Li, H.; Jia, C.; Che, C.; Wang, M.; Qin, Z. Molecules 2015, 20, 8395.
[6] Chen, W.; Wei, W.; Wu, C. C.; Li, Y. X.; Li, Y. H.; Yu, S. J.; Li, Z. M. Chin. J. Org. Chem. 2015, 35, 1576(in Chinese) (陈伟, 魏巍, 吴长春, 李玉新, 李永红, 于淑晶, 李正名, 有机化学, 2015, 35, 1576.)
[7] Chen, Y. W.; Wan, Y. Y.; Liu, Q. X.; Liu, J. B.; Xiong, L. X.; Yu, S. J.; Li, Z. M. Chin. J. Org. Chem. 2015, 35, 882(in Chinese) (陈有为, 万莹莹, 刘巧霞, 刘敬波, 熊丽霞, 于淑晶, 李正名, 有机化学, 2015, 35, 882.)
[8] Li, C. K.; Jiang, L.; Wang, Y.; Wan, F. X.; Zhang, P. Z.; Li, Y.; Cui, Z. N. Chin. J. Org. Chem. 2014, 34, 2296(in Chinese) (李成坤, 姜林, 王悦, 万福贤, 张沛之, 李映, 崔紫宁, 有机化学, 2014, 34, 2296.)
[9] Liu, X. H.; Wang, Q.; Sun, Z. H.; Wedge, D. E.; Becnel, J. J.; Estep, A. S.; Tan, C. X.; Weng, J. Q. Pest Manage. Sci. 2017, 73, 953.
[10] Chen, J. N.; Wang, X. F.; Li, T.; Wu, D. W.; Fu, X. B.; Zhang, G. J.; Shen, X. C.; Wang, H. S. Eur. J. Med. Chem. 2016, 107, 12.
[11] Liu, X. H.; Zhao, W.; Shen, Z. H.; Xing, J. H.; Yuan, J.; Yang, G.; Xu, T. M.; Peng, W. L. Bioorg. Med. Chem. Lett. 2016, 26, 3626
[12] Zhao, W.; Xing, J. H.; Xu, T. M.; Peng, W. L.; Liu, X. H. Front. Chem. Sci. Eng. 2017, 11, 363.
[13] Liu, X. H.; Zhai, Z. W.; Xu, X. Y.; Yang, M. Y.; Sun, Z. H.; Weng, J. Q.; Tan, C. X.; Chen, J. Bioorg. Med. Chem. Lett. 2015, 25, 5524.
[14] Zhai, Z. W.; Shi, Y. X.; Yang, M. Y.; Zhao, W.; Sun, Z. H.;Weng, J. Q.; Tan, C. X.; Liu, X. H.; Li, B. J.; Zhang, Y. G. Lett. Drug Des. Discovery 2016, 13, 521.
[15] Liu, X. H.; Tan, C. X.; Weng, J. Q. Phosphorus, Sulfur Silicon Relat. Elem. 2011, 186, 552.
[16] Zhang, L. J.; Yang, M. Y.; Sun, Z. H.; Tan, C. X.; Weng, J. Q.; Wu, H. K.; Liu, X. H. Lett. Drug Des. Discovery 2014, 11, 1107.
[17] Liu, X. H.; Fang, Y. M.; Xie, F.; Zhang, R. R.; Shen, Z. H.; Tan, C. X.; Weng, J. Q.; Xu, T. M.; Huang, H. Y. Pest Manage. Sci. 2017, DOI:10.1002/ps.4556.
[18] Yan, S. L.; Yang, M. Y.; Sun, Z. H.; Min, L. J.; Tan, C. X.; Weng, J. Q.; Wu, H. K.; Liu, X. H. Lett. Drug Des. Discovery 2014, 11, 940.
[19] Zhao, W.; Shen, Z. H.; Xing, J. H.; Yang, G.; Xu, T. M.; Peng, W. L.; Liu, X. H. Chem. Pap. 2017, 71, 921.
[20] Zhao, W.; Shen, Z. H.; Xing, J. H.; Xu, T. M.; Peng, W. L.; Liu, X. H. Chin. J. Struct. Chem. 2017, 36, 423.
[21] Zhao, W.; Shen, Z. H.; Xu, T. M.; Peng, W. L.; Liu, X.-H. J. Heterocycl. Chem. 2017, 54, 1751.
[22] Liu, X. H.; Zhao, W.; Shen, Z. H.; Xing, J. H.; Xu, T. M.; Peng, W. L. Eur. J. Med. Chem. 2017, 125, 881.
[23] Zhao, W.; Shen, Z. H.; Xu, T. M.; Peng, W. L.; Liu, X. H. Lett. Drug Des. Discovery 2017, 14, 323.
[24] Shen, Z. H.; Shi, Y. X.; Yang, M. Y.; Sun, Z. H.; Weng, J. Q.; Tan, C. X.; Liu, X. H.; Li, B. J.; Zhao, W. G. Chin. J. Struct. Chem.2016, 35, 457.
[25] Vasilevskii, S. F.; Shvartsberg, M. S. Bull. Acad. Sci. USSR, Chem. Sci. 1990, 39, 1901.
[26] Liu, X. H.; Tan, C. X.; Weng, J. Q. Phosphorus, Sulfur Silicon Relat. Elem. 2011, 186, 558.
[27] Zhai, Z. W.; Wang, Q.; Shen, Z. H.; Tan, C. X.; Weng, J. Q.; Liu, X. H. Chin. J. Org. Chem. 2017, 37, 232(in Chinese). (翟志文, 汪乔, 沈钟华, 谭成侠, 翁建全, 刘幸海, 有机化学, 2017, 37, 232.)

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