Synthesis and characterization of a cobalt(II) complex with 5-amino-1-tosyl-1h-1,2,4-triazole as a sulfonamide ligand: antibacterial and molecular docking studies

被引:0
|
作者
Dehghan, Parisa [1 ]
Tabatabaee, Masoumeh [1 ]
Seifati, Seyed Morteza [2 ]
Dusek, Michal [3 ]
Kucerakova, Monika [3 ]
机构
[1] Islamic Azad Univ, Dept Chem, Yazd Branch, Yazd, Iran
[2] Islamic Azad Univ, Med Biotechnol Res Ctr, Dept Biol, Ashkezar Branch, Yazd, Iran
[3] Inst Phys ASCR, Prague, Czech Republic
关键词
Sulfonamide ligands; cobalt complex; triazole derivatives; biological activity; molecular docking; X-RAY-STRUCTURE; BIOLOGICAL EVALUATION; CRYSTAL-STRUCTURE; ANTIFUNGAL; ACID;
D O I
10.1080/00958972.2024.2426156
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A new cobalt(II) complex, [Co(L)4Cl2]<middle dot>2C9H10N4O2S (1), was prepared by reaction of CoCl2<middle dot>6H2O with a sulfonamide, 5-amino-1-tosyl-1H-1,2,4-triazole (L), in double-distilled water and ethanol (1:1 v/v). The sulfonamide was characterized by elemental analysis, and infrared and 1H-NMR spectroscopy, while the Co(II) complex was characterized by elemental analysis, infrared spectroscopy, and single-crystal X-ray diffraction analysis. The X-ray structure analysis reveals that 1 consists of a mononuclear cobalt(II) complex, [Co(L)4Cl2], and two molecules of the co-crystallized ligand (5-amino-1-tosyl-1H-1,2,4-triazole). The cobalt(II) in 1 is coordinated by four triazole ligands and two chlorides in an octahedral environment. The antimicrobial activity and molecular docking of ligand and 1 were investigated. Antibacterial and antifungal activity studies of L and 1 show that both have moderate-to-significant activity against Gram-negative (Escherichia coli and Pseudomonas aeruginosa) and Gram-positive (Staphylococcus aureus and Bacillus subtilis) bacteria and fungi (Aspergillus niger and Candida albicans). According to molecular docking results, 1 could be a promising compound for developing antibacterial drugs. The docking results provide detailed evidence for the interactions of 1 with dihydropteroate synthase protein (DHPS). The microbial evaluation and molecular docking simulation results may lead to development of new drug candidates against bacterial and fungal strains.
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页数:15
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