Synthesis, Characterization, and Biological Evaluation of New Cyclic Quinazoline Derivatives as Potential Antibacterial and Antifungal Agents

被引:0
作者
Al-Jeilawi, Oday H. R. [1 ]
Tuama, Safaa H. F. [1 ]
Hussein, Iftikhar A. [1 ]
Shamaya, Andy N. S. [1 ]
机构
[1] Univ Baghdad, Coll Sci, Dept Chem, Baghdad 10071, Iraq
基金
英国科研创新办公室;
关键词
novel heterocycle; antibacterial; antifungal; quinazoline; ring closure; HETEROCYCLES; BACTERIAL;
D O I
10.1134/S0012500823600554
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Heterocyclic compounds are crucial for medicinal chemistry and the development of therapeutic agents like broad-spectrum antibiotics. This study devised a facile procedure to synthesize novel antimicrobial bicyclic heterocycles from 2-mercapto-3-phenylquinazolin-4(3H)-one. Advanced analytical techniques including H-1 and C-13 NMR, elemental analysis, and FT-IR spectroscopy characterized the intricate chemical structures of the products. In vitro assays tested the heterocycles against aerobic and anaerobic bacterial strains using fluconazole and ciprofloxacin as antifungal and antibacterial controls. Results demonstrated the formidable broad-spectrum antibacterial and antifungal activities of the synthesized compounds, with growth inhibition approaching that of the positive controls. These findings highlight the immense potential of these novel heterocyclic compounds as antimicrobial agents. Further research can optimize their drug-like properties for eventual clinical use in combating drug-resistant infections.
引用
收藏
页码:27 / 34
页数:8
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