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首页> 外文期刊>Journal of enzyme inhibition and medicinal chemistry. >Antibacterial Schiff bases of oxalyl-hydrazine/diamide incorporating pyrrolyl and salicylyl moieties and of their zinc(II) complexes.
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Antibacterial Schiff bases of oxalyl-hydrazine/diamide incorporating pyrrolyl and salicylyl moieties and of their zinc(II) complexes.

机译:草酰肼/二酰胺结合了吡咯基和水杨基部分的抗菌席夫碱及其锌(II)配合物。

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摘要

Schiff bases derived from oxaldiamide/oxalylhydrazine and pyrrol-2-carbaldehyde, or salicylaldehyde respectively, as well as their Zn(II) complexes have been prepared and tested as antibacterial agents. These Schiff bases function as tetradentate ligands, forming octahedral Zn(II) complexes. The ketonic form for the diamide derived Schiff base and the enolic form of the hydrazide derived Schiff base were the preferred tautomers for coordination of the metal ions. The title compounds and their Zn(II) derivatives were evaluated for antibacterial activity against several bacterial strains which easily develop resistance to classical antibiotics, such as Escherichia coli, Staphylococcus aureus and Pseudomonas aeruginosa. Some of them showed promising biological activity in inhibiting the growth of such organisms.
机译:已经制备了分别衍生自草二酰胺/草酰肼和吡咯-2-甲醛或水杨醛的席夫碱,以及它们的Zn(II)配合物,并作为抗菌剂进行了测试。这些席夫碱起四齿配体的作用,形成八面体Zn(II)络合物。二酰胺衍生的席夫碱的酮形式和酰肼衍生的席夫碱的烯醇形式是用于金属离子配位的优选互变异构体。评估了标题化合物及其Zn(II)衍生物对几种细菌菌株的抗菌活性,这些细菌菌株容易对经典抗生素(如大肠杆菌,金黄色葡萄球菌和铜绿假单胞菌)产生抗药性。它们中的一些在抑制此类生物的生长方面显示出有希望的生物学活性。

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