Cu(II) Complexes of New Sulfa Drug Schiff Base Ligands: Synthesis, Structural Characterization, Antimicrobial Activities, and Time-Killing Kinetics

被引:2
|
作者
Sahal, Hakan [1 ]
Idil, Onder [2 ]
Canpolat, Erdal [3 ]
Ozkan, Mustafa [4 ]
机构
[1] Munzur Univ, Vocat Sch Tunceli, Dept Food Proc, TR-62000 Tunceli, Turkiye
[2] Amasya Univ, Educ Fac, Dept Basic Educ, TR-05100 Amasya, Turkiye
[3] Firat Univ, Fac Educ, Dept Elementary Sci Educ, TR-23200 Elazig, Turkiye
[4] Bursa Uludag Univ, Fac Educ, Dept Elementary Sci Educ, TR-16059 Bursa, Turkiye
关键词
sulfa drug; Schiff base; Cu(II) complex; antimicrobial activity; time killing; ANTICANCER ACTIVITY; CARBONIC-ANHYDRASE; SULFONAMIDES; DERIVATIVES; INHIBITORS; SERIES;
D O I
10.1134/S1068162023030184
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Synthesis of three different new sulfonamide compounds (L-1-L-3) and their Cu(II) complexes were carried out. Their structures were characterized by spectroscopic methods such as Fourier transform infrared, Proton nuclear magnetic resonance and elemental analysis. Cu(II) complexes were screened for Gram-positive, Gram-negative bacteria and against yeast using the microdilution method. In particular, CuL2 was found to have significant antimicrobial effects on Gram (-), Gram (+) and eukaryotic yeast. The results showed that CuL2 exhibited better antimicrobial activity than other complexes. Depending on the antimicrobial activity results, time killing experiments of CuL2, the most effective complex, were performed.
引用
收藏
页码:602 / 609
页数:8
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