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噻二唑衍生的呋喃基、噻吩基和吡咯基席夫碱的抗菌钴(II)、铜(II)、镍(II)和锌(II)配合物

Antibacterial Co(II), Cu(II), Ni(II) and Zn(II) complexes of thiadiazole derived furanyl, thiophenyl and pyrrolyl Schiff bases.

作者信息

Chohan Zahid H, Pervez Humayun, Rauf Abdul, Scozzafava Andrea, Supuran Claudiu T

机构信息

Department of Chemistry, Islamia University, Bahawalpur, Pakistan.

出版信息

J Enzyme Inhib Med Chem. 2002 Apr;17(2):117-22. doi: 10.1080/14756360290024218.

Abstract

2-Amino-1,3,4-thiadiazole undergoes a condensation reaction with furane-, thiophene- and pyrrole-2-carboxaldehyde to form tridentate NNO, NNS and NNN donor Schiff bases. These Schiff bases were further used to obtain complexes of the type [M(L)2]X, where M = Co(II), Cu(II), Ni(II) or Zn(II), L = L1, L2 or L3 and X = Cl2. The new compounds described here have been characterized by their physical, spectral and analytical data, and have been screened for antibacterial activity against several bacterial strains such as Escherichia coli, Staphylococcus aureus, and Pseudomonas aeruginosa. The antibacterial potency of the Schiff bases increased upon chelation/complexation in comparison to the uncomplexed Schiff bases against the tested bacterial species thus, opening new approaches to find new ways in the fight against antibiotic-resistant strains.

摘要

2-氨基-1,3,4-噻二唑与呋喃-2-甲醛、噻吩-2-甲醛和吡咯-2-甲醛发生缩合反应,形成三齿NNO、NNS和NNN供体席夫碱。这些席夫碱进一步用于制备[M(L)2]X型配合物,其中M = Co(II)、Cu(II)、Ni(II)或Zn(II),L = L1、L2或L3,X = Cl2。本文描述的新化合物已通过其物理、光谱和分析数据进行了表征,并针对几种细菌菌株(如大肠杆菌、金黄色葡萄球菌和铜绿假单胞菌)进行了抗菌活性筛选。与未配位的席夫碱相比,席夫碱在螯合/配位后对测试细菌物种的抗菌效力增强,从而为寻找对抗抗生素耐药菌株的新方法开辟了新途径。

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