Citation: Wang Yurong, Zheng Dandan, Wang Yang, Ye Hao, Yao Wei, Ding Ying, Gu Haiying, Feng Xia, Li Ling, Dai Hong. Synthesis and Bioactivities of Novel Pyrazole Oxime Ethers Containing 1, 2, 4-Triazole Moiety[J]. Chinese Journal of Organic Chemistry, ;2019, 39(7): 2053-2061. doi: 10.6023/cjoc201902027 shu

Synthesis and Bioactivities of Novel Pyrazole Oxime Ethers Containing 1, 2, 4-Triazole Moiety

  • Corresponding author: Gu Haiying, guhy99@21cn.com Dai Hong, daihong_2015@aliyun.com
  • These authors contributed equally to this work
  • Received Date: 25 February 2019
    Revised Date: 22 March 2019
    Available Online: 2 July 2019

    Fund Project: the National Natural Science Foundation of China 21475070the National Natural Science Foundation of China 21372135Project supported by the National Natural Science Foundation of China (Nos. 21874077, 21475070, 21372135), and the Science and Technology Project Fund of Nantong City (No. MS12017022-4)the Science and Technology Project Fund of Nantong City MS12017022-4the National Natural Science Foundation of China 21874077

Figures(3)

  • Eighteen novel pyrazole oxime ethers containing 1, 2, 4-triazole moiety were designed and synthesized according to the method of active substructure combination. Their structures were characterized by 1H NMR, 13C NMR, and elemental analyses. Preliminary bioassay showed that some target compounds showed good insecticidal activities against Oriental armyworm, Aphis medicaginis and Tetranychus cinnabarinus. At the concentration of 500 μg/mL, target compounds had insecticidal activity against Oriental armyworm with 90%~100%, which were similar to the control of avermectin, four compounds showed 100% insecticidal activity against Aphis medicaginis, which were similar to imidacloprid. The lethal rate of 1- methyl-3-methyl-5-(3, 5-difluorophenoxy)-1H-pyrazole-4-carbaldehyde-O-[4-(1H-1, 2, 4-triazol-1-yl)phenylmethyl]oxime (8p) against Tetranychus cinnabarinus was 100%, which was similar to that of fenpyroximate. When the concentration was reduced to 100 μg/mL, six compounds exhibited insecticidal activity against Oriental armyworm with 90%~100%, three compounds showed insecticidal activity against Aphis medicaginis with 80%~100%, and compound 8p had acaricidal activity against Tetranychus cinnabarinus with 80%. At the concentration of 20 μg/mL, the lethal rates of two compounds against Oriental armyworm were 75% and 70%, respectively. Additionally, some compounds exhibited certain anti-tumor activity against human hepatocellular carcinoma SMMC-7721 cells.
  • 加载中
    1. [1]

      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.  doi: 10.1016/j.bmcl.2016.06.004

    2. [2]

      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).
       

    3. [3]

      Liu, X. H.; Zhao, W.; Shen, Z. H.; Xing, J. H.; Xu, T. M.; Peng, W. L. Eur. J. Med. Chem. 2017, 125, 881.  doi: 10.1016/j.ejmech.2016.10.017

    4. [4]

      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.  doi: 10.1002/ps.4370

    5. [5]

      Shi, J. J.; Ren, G. H.; Wu, N. J.; Weng, J. Q.; Xu, T. M.; Liu, X. H.; Tan, C. X. Chin. Chem. Lett. 2017, 28, 1727.  doi: 10.1016/j.cclet.2017.05.015

    6. [6]

      Li, Q. M.; Pang, K. S.; Zhao, J. P.; Liu, X. H.; Weng, J. Q. Chin. J. Org. Chem. 2017, 37, 1009(in Chinese).
       

    7. [7]

      Dai, X. Q.; Zhu, Y. B.; Wang, Z. Y.; Weng, J. Q. Chin. J. Org. Chem. 2017, 37, 1924(in Chinese).
       

    8. [8]

      Shi, J. J.; Ren, G. H.; Dai, Z. M.; Wu, N, J.; Weng, J. Q.; Xu, T. M.; Liu, X. H.; Tan, C. X. Lett. Drug Des. Discovery 2018, 15, 15.

    9. [9]

      Shen, Z. H.; Sun, Z. H.; Becnel, J. J.; Estep, A.; Wedge, D. E.; Tan, C. X.; Weng, J. Q.; Han, L.; Liu, X. H. Lett. Drug Des. Discovery 2018, 15, 951.  doi: 10.2174/1570180815666180102141640

    10. [10]

      Chen, L.; Shen, Z. H.; Xu, T. M.; Tan, C. X.; Weng, J. Q.; Han, L.; Peng. W. L.; Liu, X. H. J. Heterocycl. Chem. 2018, 55, 946.  doi: 10.1002/jhet.3123

    11. [11]

      Li, Y.; Zhang, H. Q.; Liu, J.; Yang, X. P.; Liu, Z. J. J. Agric. Food Chem. 2006, 54, 3636.  doi: 10.1021/jf060074f

    12. [12]

      Ouyang, G. P.; Cai, X. J.; Chen, Z.; Song, B. A.; Bhadury, P. S.; Yang, S.; Jin, L. H.; Xue, W.; Hu, D. Y.; Zeng, S. J. Agric. Food Chem. 8, 56, 10160.  doi: 10.1021/jf802489e

    13. [13]

      Wang, S. L.; Shi, Y. J.; He, H. B.; Li, Y.; Li, Y.; Dai, H. Chin. Chem. Lett. 2015, 26, 672.  doi: 10.1016/j.cclet.2015.04.017

    14. [14]

      Dai, H.; Ge, S. S.; Guo, J.; Chen, S.; Huang, M. L.; Yang. J. Y.; Sun, S. Y.; Ling, Y.; Shi, Y. J. Eur. J. Med. Chem. 2018, 143, 1066.  doi: 10.1016/j.ejmech.2017.11.098

    15. [15]

      Hamaguchi, H.; Kajihara, O.; Katoh, M. J. Pestic. Sci. 1995, 20, 173.  doi: 10.1584/jpestics.20.173

    16. [16]

      Fu, C. R.; Peng, J.; Ning, Y.; Liu, M.; Shan, P. C.; Liu, J.; Li, Y. Q.; Hu, F. Z.; Zhu, Y. Q.; Yang, H. Z.; Zou, X. M. Pest Manage. Sci. 2014, 70, 1207.  doi: 10.1002/ps.3672

    17. [17]

      Dai, H.; Xiao, Y. S.; Li, Z.; Xu, X. Y.; Qian, X. H. Chin. Chem. Lett. 2014, 25, 1014.  doi: 10.1016/j.cclet.2014.06.011

    18. [18]

      Zhou, Q.; Zheng, D. D.; Shi, Y. J.; Yao, W.; Qian, H. W.; Ding, Y.; Wei, Z. H.; Shen, A. Y.; Feng, X.; Shi, J.; Dai, H. Chin. J. Org. Chem. 2018, 38, 3318(in Chinese).
       

    19. [19]

      Lü, X. H.; Li, Q. S.; Ren, Z. L.; Chu, M. J.; Sun, J.; Zhang, X.; Xing, M.; Zhu, H. L.; Cao, H. Q. Eur. J. Med. Chem. 2015, 108, 586.

    20. [20]

      Dai, H.; Ge, S. S.; Li, G.; Chen, J.; Shi, Y. J.; Ye, L. Y.; Ling, Y. Bioorg. Med. Chem. Lett. 2016, 26, 4504.  doi: 10.1016/j.bmcl.2016.07.068

    21. [21]

      Clark, R. L.; Clements, C. J.; Barrett, M. P.; Mackay, S. P.; Rathnam, R. P.; Owusu-Dapaah, G.; Spencer, J.; Huggan, J. K. Bioorg. Med. Chem. Lett. 2012, 20, 6019.  doi: 10.1016/j.bmc.2012.08.049

    22. [22]

      Jia, C. Q.; Su, W. C.; Xu, Y. J.; Liu, J. P.; Qin, Z. H. Chin. J. Org. Chem. 2016, 36, 830(in Chinese).
       

    23. [23]

      Wang, H. L.; Ruan, L. L.; Chen, Y.; Liu, X. H.; Weng, J. Q. Chin. J. Org. Chem. 2014, 34, 419(in Chinese).
       

    24. [24]

      El-Helby, A. G. A. Bull. Pharm. Sci. 2005, 28, 45.

    25. [25]

      El-Sherief, H. A. M.; Youssif, B. G.; Bukhari, S. N. A.; Abdelazeem, A. H.; Abdel-Aziz, M.; Abdel-Rahman, H. M. Eur. J. Med. Chem. 2018, 156, 774.  doi: 10.1016/j.ejmech.2018.07.024

    26. [26]

      Jia, C. Q.; Yang, D. Y.; Che, C. L.; Ma, Y. Q.; Rui, C. H.; Yan, X. J.; Qin, Z. H. Chem. J. Chin. Univ. 2016, 37, 892(in Chinese).
       

    27. [27]

      Wang, H. L.; Ruan, L. L.; Chen, Y.; Liu, X. H.; Weng, J. Q. Chin. J. Org. Chem. 2018, 38, 2137(in Chinese). 

    28. [28]

      Park, M. S.; Park, H. J.; Park, K. H.; Lee, K. I. Synth. Commun. 2004, 34, 1541.  doi: 10.1081/SCC-120030741

    29. [29]

      Park, H. J.; Lee, K.; Park, S. J.; Ahn, B.; Lee, J. C.; Cho, H. Y.; Lee, K. I. Bioorg. Med. Chem. Lett. 2005, 15, 3307.  doi: 10.1016/j.bmcl.2005.03.082

    30. [30]

      Tanaka, A.; Terasawa, T.; Hagihara, H.; Sakuma, Y.; Ishibe, N.; Sawada, M.; Takasugi, H.; Tanaka, H. J. Med. Chem. 1998, 41, 2390.  doi: 10.1021/jm9800853

    31. [31]

      Liu, J. C.; Liu, Y. J.; He, H. W. Chin. J. Org. Chem. 2015, 35, 462(in Chinese).
       

  • 加载中
    1. [1]

      Lifang HEWenjie TANGYaoze LUOMingsheng LIANGJianxin TANGYuxuan WUFuxing ZHANGXiaoming ZHU . Synthesis, structure, and anticancer activity of two dialkyltin complexes constructed based on 2, 2′-bipyridin-6, 6′-dicarboxylic acid. Chinese Journal of Inorganic Chemistry, 2025, 41(8): 1601-1609. doi: 10.11862/CJIC.20250012

    2. [2]

      Xin MAYa SUNNa SUNQian KANGJiajia ZHANGRuitao ZHUXiaoli GAO . A Tb2 complex based on polydentate Schiff base: Crystal structure, fluorescence properties, and biological activity. Chinese Journal of Inorganic Chemistry, 2024, 40(7): 1347-1356. doi: 10.11862/CJIC.20230357

    3. [3]

      Bin SUNHeyan JIANG . Glucose-modified bis-Schiff bases: Synthesis and bio-activities in Alzheimer′s disease therapy. Chinese Journal of Inorganic Chemistry, 2025, 41(7): 1338-1350. doi: 10.11862/CJIC.20240428

    4. [4]

      Jing WUPuzhen HUIHuilin ZHENGPingchuan YUANChunfei WANGHui WANGXiaoxia GU . Synthesis, crystal structures, and antitumor activities of transition metal complexes incorporating a naphthol-aldehyde Schiff base ligand. Chinese Journal of Inorganic Chemistry, 2024, 40(12): 2422-2428. doi: 10.11862/CJIC.20240278

    5. [5]

      Xinting XIONGZhiqiang XIONGPanlei XIAOXuliang NIEXiuying SONGXiuguang YI . Synthesis, crystal structures, Hirshfeld surface analysis, and antifungal activity of two complexes Na(Ⅰ)/Cd(Ⅱ) assembled by 5-bromo-2-hydroxybenzoic acid ligands. Chinese Journal of Inorganic Chemistry, 2024, 40(9): 1661-1670. doi: 10.11862/CJIC.20240145

    6. [6]

      Haitang WANGYanni LINGXiaqing MAYuxin CHENRui ZHANGKeyi WANGYing ZHANGWenmin WANG . Construction, crystal structures, and biological activities of two Ln3 complexes. Chinese Journal of Inorganic Chemistry, 2024, 40(8): 1474-1482. doi: 10.11862/CJIC.20240188

    7. [7]

      Siran Wang Yinuo Wang Yilong Zhao Dazhen Xu . Advances in the Application and Preparation of Rhodanine and Its Derivatives. University Chemistry, 2025, 40(5): 318-327. doi: 10.12461/PKU.DXHX202407033

    8. [8]

      Jiaming Xu Yu Xiang Weisheng Lin Zhiwei Miao . Research Progress in the Synthesis of Cyclic Organic Compounds Using Bimetallic Relay Catalytic Strategies. University Chemistry, 2024, 39(3): 239-257. doi: 10.3866/PKU.DXHX202309093

    9. [9]

      Xinyi ZhangKai RenYanning LiuZhenyi GuZhixiong HuangShuohang ZhengXiaotong WangJinzhi GuoIgor V. ZatovskyJunming CaoXinglong Wu . Progress on Entropy Production Engineering for Electrochemical Catalysis. Acta Physico-Chimica Sinica, 2024, 40(7): 2307057-0. doi: 10.3866/PKU.WHXB202307057

    10. [10]

      Lei FengZe-Min ZhuYing YangZongbin HeJiafeng ZouMan-Bo LiYan ZhaoZhikun Wu . Long-Pursued Structure of Au23(S-Adm)16 and the Unexpected Doping Effects. Acta Physico-Chimica Sinica, 2024, 40(5): 2305029-0. doi: 10.3866/PKU.WHXB202305029

    11. [11]

      Chunling QinShuang ChenHassanien GomaaMohamed A. ShenashenSherif A. El-SaftyQian LiuCuihua AnXijun LiuQibo DengNing Hu . Regulating HER and OER Performances of 2D Materials by the External Physical Fields. Acta Physico-Chimica Sinica, 2024, 40(9): 2307059-0. doi: 10.3866/PKU.WHXB202307059

    12. [12]

      Liping GUO . Synthesis and crystal structure characterization of yttrium imido complex: The reactivity of 2-substituted-1-amino-o-carborane with yttrium dialkyl complex. Chinese Journal of Inorganic Chemistry, 2025, 41(7): 1409-1415. doi: 10.11862/CJIC.20250065

    13. [13]

      Tianlong Zhang Rongling Zhang Hongsheng Tang Yan Li Hua Li . Online Monitoring and Mechanistic Analysis of 3,5-diamino-1,2,4-triazole (DAT) Synthesis via Raman Spectroscopy: A Recommendation for a Comprehensive Instrumental Analysis Experiment. University Chemistry, 2024, 39(6): 303-311. doi: 10.3866/PKU.DXHX202312006

    14. [14]

      Jingjing QINGFan HEZhihui LIUShuaipeng HOUYa LIUYifan JIANGMengting TANLifang HEFuxing ZHANGXiaoming ZHU . Synthesis, structure, and anticancer activity of two complexes of dimethylglyoxime organotin. Chinese Journal of Inorganic Chemistry, 2024, 40(7): 1301-1308. doi: 10.11862/CJIC.20240003

    15. [15]

      Maitri BhattacharjeeRekha Boruah SmritiR. N. Dutta PurkayasthaWaldemar ManiukiewiczShubhamoy ChowdhuryDebasish MaitiTamanna Akhtar . Synthesis, structural characterization, bio-activity, and density functional theory calculation on Cu(Ⅱ) complexes with hydrazone-based Schiff base ligands. Chinese Journal of Inorganic Chemistry, 2024, 40(7): 1409-1422. doi: 10.11862/CJIC.20240007

    16. [16]

      Yahui HANJinjin ZHAONing RENJianjun ZHANG . Synthesis, crystal structure, thermal decomposition mechanism, and fluorescence properties of benzoic acid and 4-hydroxy-2, 2′: 6′, 2″-terpyridine lanthanide complexes. Chinese Journal of Inorganic Chemistry, 2025, 41(5): 969-982. doi: 10.11862/CJIC.20240395

    17. [17]

      Aidang Lu Yunting Liu Yanjun Jiang . Comprehensive Organic Chemistry Experiment: Synthesis and Characterization of Triazolopyrimidine Compounds. University Chemistry, 2024, 39(8): 241-246. doi: 10.3866/PKU.DXHX202401029

    18. [18]

      Yihui Song Shangshang Qin Kai Wu Chengyun Jin Bin Yu . 生物化学在高水平创新型药学人才培养中的交叉融合应用——以去甲基化酶LSD1抑制剂的活性评价为例. University Chemistry, 2025, 40(6): 341-352. doi: 10.12461/PKU.DXHX202406018

    19. [19]

      Yajin LiHuimin LiuLan MaJiaxiong LiuDehua He . Photothermal Synthesis of Glycerol Carbonate via Glycerol Carbonylation with CO2 over Au/Co3O4-ZnO Catalyst. Acta Physico-Chimica Sinica, 2024, 40(9): 2308005-0. doi: 10.3866/PKU.WHXB202308005

    20. [20]

      Yongqing Kuang Jie Liu Jianjun Feng Wen Yang Shuanglian Cai Ling Shi . Experimental Design for the Two-Step Synthesis of Paracetamol from 4-Hydroxyacetophenone. University Chemistry, 2024, 39(8): 331-337. doi: 10.12461/PKU.DXHX202403012

Metrics
  • PDF Downloads(4)
  • Abstract views(1167)
  • HTML views(130)

通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索
Address:Zhongguancun North First Street 2,100190 Beijing, PR China Tel: +86-010-82449177-888
Powered By info@rhhz.net

/

DownLoad:  Full-Size Img  PowerPoint
Return