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首页> 外文期刊>Bioorganic and medicinal chemistry >Synthesis, crystal structures, and urease inhibition of an acetohydroxamate-coordinated oxovanadium(V) complex derived from N '-(3-bromo-2-hydroxybenzylidene)-4-methoxybenzohydrazide
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Synthesis, crystal structures, and urease inhibition of an acetohydroxamate-coordinated oxovanadium(V) complex derived from N '-(3-bromo-2-hydroxybenzylidene)-4-methoxybenzohydrazide

机译:N'-(3-溴-2-羟基苄叉)-4-甲氧基苯甲酰肼衍生的乙酰氧肟酸酯配位的氧钒(V)配合物的合成,晶体结构和脲酶抑制

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摘要

A new benzohydrazone compound N0-(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 H-1 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 mu mol.L-1 on Helicobacter pylori urease is 78% for the oxovanadium complex. The IC50 value for the complex is 36.5 mu mol.L-1. Molecular docking study was performed to study the inhibition. (C) 2015 Elsevier Ltd. All rights reserved.
机译:制备了新的苯并hydr化合物N0-(3-溴-2-羟基亚苄基)-4-甲氧基苯并肼(H2L)。 H2L和乙酰氧肟酸(HAHA)与VO(acac)(2)在甲醇中的反应生成配合物[VOL(AHA)]。通过元素分析,IR,UV-vis和H-1 NMR光谱以及单晶X射线衍射对H2L和氧钒配合物进行表征。 H2L的特征还在于高分辨率质谱。进行氧钒钒配合物的热分析。苯并hydr配体为二价阴离子形式,通过苯酚氧,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配位至V原子。 V原子处于八面体配位状态。测试了H2L,HAHA和氧钒钠复合物的脲酶抑制活性。对于氧钒络合物,在100μmol.L-1的浓度下,幽门螺杆菌脲酶的抑制百分比为78%。该配合物的IC 50值为36.5μmol.L-1。进行分子对接研究以研究抑制作用。 (C)2015 Elsevier Ltd.保留所有权利。

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