酰腙氧钒(Ⅴ)配合物的合成、结构及其抑制幽门螺旋杆菌脲酶研究

赵月 韩笑 周晓霞 李海华 由忠录

引用本文: 赵月, 韩笑, 周晓霞, 李海华, 由忠录. 酰腙氧钒(Ⅴ)配合物的合成、结构及其抑制幽门螺旋杆菌脲酶研究[J]. 无机化学学报, 2013, 29(4): 867-874. doi: 10.3969/j.issn.1001-4861.2013.00.140 shu
Citation:  ZHAO Yue, HAN Xiao, ZHOU Xiao-Xia, LI Hai-Hua, YOU Zhong-Lu. Synthesis, Structures, and Helicobacter Pylori Urease Inhibition of Oxovanadium(Ⅴ) Complexes with Hydrazones[J]. Chinese Journal of Inorganic Chemistry, 2013, 29(4): 867-874. doi: 10.3969/j.issn.1001-4861.2013.00.140 shu

酰腙氧钒(Ⅴ)配合物的合成、结构及其抑制幽门螺旋杆菌脲酶研究

  • 基金项目:

    国家自然科学基金(No.20901036) (No.20901036)

    辽宁省高校优秀青年人才支持计划(No.LJQ2011114)资助项目。 (No.LJQ2011114)

摘要: 为了探索新型高效脲酶抑制剂, 本文合成了2个新的酰腙氧钒(Ⅴ)配合物, [VOL1(OCH3)(CH3OH)] (1)和[VOL2(μ-OCH3)]2 (2)(H2L1=N′-(5-氯-2-羟基苯亚甲基)-3-硝基苯甲酰肼;H2L2=N′-(5-氯-2-羟基苯亚甲基)-4-氯苯甲酰肼), 并通过物理化学方法和单晶X-射线衍射表征了它们的结构。化合物1是一个单核配合物, 而化合物2是由两个甲氧基配体桥连的具有中心对称性的双核配合物。在每个配合物中, V原子都采取八面体配位构型。本文还研究了这两个配合物的热稳定性和它们对幽门螺旋杆菌脲酶的抑制活性。在浓度为100 μmol·L-1时, 配合物1和2对脲酶的抑制率分别为71.4%和73.3%, 其IC50值分别为63.6和37.7 μmol·L-1

English

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  • 收稿日期:  2012-12-27
  • 网络出版日期:  2013-01-17
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