Chin. J. Org. Chem. ›› 2019, Vol. 39 ›› Issue (2): 491-499.DOI: 10.6023/cjoc201806042 Previous Articles     Next Articles

ARTICLE

新型含咔唑环酰腙衍生物的合成及Cdc25B/PTP1B抑制活性评价

李英俊a, 王思远a, 靳焜b, 高立信c, 盛丽c, 张楠a, 刘季红d, 李佳c   

  1. a 辽宁师范大学化学化工学院 大连 116029;
    b 大连理工大学精细化工国家重点实验室 大连 116012;
    c 中国科学院上海药物研究所 国家新药筛选中心药物研究国家重点实验室 上海 201203;
    d 大连理工大学 化环生学部分析测试中心 大连 116023
  • 收稿日期:2018-06-27 修回日期:2018-08-22 发布日期:2018-09-10
  • 通讯作者: 李佳 E-mail:chemlab.lnnu@163.com
  • 基金资助:

    辽宁省自然科学基金(No.20102126)资助项目.

Synthesis and Cdc25B/PTP1B Inhibitory Activity Evaluation of Novel Acylhydrazone Derivatives Containing Carbazole Moity

Li Yingjuna, Wang Siyuana, Jin Kunb, Gao Lixinc, Sheng Lic, Zhang Nana, Liu Jihongd, Li Jiac   

  1. a College of Chemistry and Chemical Engineering, Liaoning Normal University, Dalian 116029;
    b State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian 116012;
    c State Key Laboratory of Drug Research, National Center for Drug Screening, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203;
    d Chemistry Analysis & Research Center, Faculty of Chemical, Environmental & Biological Science and Technology, Dalian University of Technology, Dalian 116023
  • Received:2018-06-27 Revised:2018-08-22 Published:2018-09-10
  • Contact: 10.6023/cjoc201806042 E-mail:chemlab.lnnu@163.com
  • Supported by:

    Project supported by the Natural Science Foundation of Liaoning Province (No. 20102126).

A series of novel acylhydrazone derivatives 6 containing carbazole moity were synthesized by carbazole and 4-cyanobenzyl chloride as starting materials via multi-step reactions. Their structures were characterized by IR, 1H NMR, 13C NMR spectra and elemental analysis. All synthesized target compounds were evaluated for the inhibitory activities against Cdc25B and PTP1B. The results show that the target compounds display significant inhibitory activities against Cdc25B/PTP1B. Among them, compound 4-((carbazol-9-yl)methyl)-N'-(2-hydroxy-1-naphthalenylmethylene)benzoyl hydrazide (6g) had the highest inhibitory activities against Cdc25B and PTP1B with IC50 values of (2.16±0.38) and (1.06±0.23) μg/mL, respectively. The molecular docking results indicated that the hydrogen bond and hydrophobic interaction formed between compound 6g and Cdc25B/PTP1B enzyme.

Key words: acylhydrazone, carbazole, synthesis, Cdc25B and PTP1B inhibitor, molecular docking