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由N'-(3-溴-2-羟基亚苄基)-4-甲氧基苯甲酰肼衍生的乙酰氧肟酸配位的氧钒(V)配合物的合成、晶体结构及脲酶抑制作用

Synthesis, crystal structures, and urease inhibition of an acetohydroxamate-coordinated oxovanadium(V) complex derived from N'-(3-bromo-2-hydroxybenzylidene)-4-methoxybenzohydrazide.

作者信息

Qu Dan, Niu Fang, Zhao Xinlu, Yan Ke-Xiang, Ye Yu-Ting, Wang Jia, Zhang Mei, You Zhonglu

机构信息

Department of Chemistry and Chemical Engineering, Liaoning Normal University, Dalian 116029, PR China.

Department of Dermatology, Huashan Hospital, Shanghai 200040, PR China.

出版信息

Bioorg Med Chem. 2015 May 1;23(9):1944-9. doi: 10.1016/j.bmc.2015.03.036. Epub 2015 Mar 20.

Abstract

A new benzohydrazone compound N'-(3-bromo-2-hydroxybenzylidene)-4-methoxybenzohydrazide (H₂L) was prepared. Reaction of H₂L and acetohydroxamic acid (HAHA) with VO(acac)₂ in methanol gave the complex [VOL(AHA)]. Both H₂L and the oxovanadium complex were characterized by elemental analysis, IR, UV-vis and (1)H NMR spectra, and single crystal X-ray diffraction. H₂L was also characterized by high-resolution mass spectrum. Thermal analysis of the oxovanadium complex was carried out. The benzohydrazone ligand, in its dianionic form, coordinates to V atom through the phenolate oxygen, imino nitrogen and enolate oxygen. The acetohydroxamic acid coordinates to V atom through the carbonyl oxygen and deprotonated hydroxyl oxygen. The V atom is in octahedral coordination. H₂L, HAHA and the oxovanadium complex were tested for their urease inhibitory activities. The percent inhibition at concentration of 100 μmol·L(-1) on Helicobacter pylori urease is 78% for the oxovanadium complex. The IC₅₀ value for the complex is 36.5 μmol·L(-1). Molecular docking study was performed to study the inhibition.

摘要

制备了一种新型苯腙化合物N'-(3-溴-2-羟基亚苄基)-4-甲氧基苯甲酰肼(H₂L)。H₂L和乙酰氧肟酸(HAHA)与VO(acac)₂在甲醇中反应得到配合物[VOL(AHA)]。通过元素分析、红外光谱、紫外可见光谱和¹H NMR光谱以及单晶X射线衍射对H₂L和氧钒配合物进行了表征。H₂L还通过高分辨率质谱进行了表征。对氧钒配合物进行了热分析。苯腙配体以其二阴离子形式通过酚氧、亚氨基氮和烯醇氧与V原子配位。乙酰氧肟酸通过羰基氧和去质子化的羟基氧与V原子配位。V原子呈八面体配位。测试了H₂L、HAHA和氧钒配合物的脲酶抑制活性。对于氧钒配合物,在100 μmol·L⁻¹浓度下对幽门螺杆菌脲酶的抑制率为78%。该配合物的IC₅₀值为36.5 μmol·L⁻¹。进行了分子对接研究以研究抑制作用。

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