Synthesis, characterization, crystal structures and urease inhibitory activity of new acylhydrazone complex materials.

IF 1.2 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Feng-Qian Zou, De-Wen Dong
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引用次数: 0

Abstract

In this work, four new oxidovanadium(V) complexes with the general formula [VOLL'] were prepared. L is the dianionic form of 2-hydroxy-5-methyl-N'-(3-methylbenzylidene)benzohydrazide (H2L1) for complexes 1 and 2, and 2-hydroxy-4-methoxy-N'-(3-methylbenzylidene)benzohydrazide (H2L2) for complexes 3 and 4. L' is the deprotonated form of methyl maltol (HLa) for complexes 1 and 3, and ethyl maltol (HLb) for complexes 2 and 4. The structural features of the complexes were assigned using the single crystal X-ray diffraction and other physicochemical techniques. The V atoms in the complexes are in octahedral coordination. Inhibitory activities of the acylhydrazones and complexes were evaluated on Helicobacter pylori urease. All the complexes show effective activity with IC50 values of 15.3-27.2 μmol L-1.

新型酰基腙配合物的合成、表征、晶体结构及脲酶抑制活性。
本文制备了四种新的氧化钒配合物,其通式为[VOLL']。L是配合物1和2的2-羟基-5-甲基- n '-(3-甲基苄基)苯并肼(H2L1)和配合物3和4的2-羟基-4-甲氧基- n '-(3-甲基苄基)苯并肼(H2L2)的二阴离子形式。L′是配合物1和3的甲基麦芽糖醇(HLa)的去质子化形式,配合物2和4的乙基麦芽糖醇(HLb)。利用单晶x射线衍射和其他物理化学技术确定了配合物的结构特征。配合物中的V原子呈八面体配位。评价了酰基腙及其配合物对幽门螺杆菌脲酶的抑制活性。所有配合物均显示有效活性,IC50值为15.3 ~ 27.2 μmol L-1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta Chimica Slovenica
Acta Chimica Slovenica 化学-化学综合
CiteScore
2.50
自引率
25.00%
发文量
80
审稿时长
1.0 months
期刊介绍: Is an international, peer-reviewed and Open Access journal. It provides a forum for the publication of original scientific research in all fields of chemistry and closely related areas. Reviews, feature, scientific and technical articles, and short communications are welcome.
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