Synthesis and Antimicrobial Activity of Novel Benzoxazoles

被引:17
作者
Arisoy, Mustafa [1 ]
Temiz-Arpaci, Ozlem [1 ]
Kaynak-Onurdag, Fatma [2 ]
Ozgen, Selda [2 ]
机构
[1] Ankara Univ, Fac Pharm, Dept Pharmaceut Chem, TR-06100 Ankara, Turkey
[2] Gazi Univ, Fac Pharm, Dept Pharmaceut Microbiol, TR-06330 Ankara, Turkey
来源
ZEITSCHRIFT FUR NATURFORSCHUNG SECTION C-A JOURNAL OF BIOSCIENCES | 2012年 / 67卷 / 9-10期
关键词
Benzoxazoles; Antibacterial Activity; Antifungal Activity; BIOLOGICAL-ACTIVITY; ANALOGS;
D O I
10.5560/ZNC.2012.67c0466
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
Z. Naturforsch. 67c, 466-472 (2012); received October 17, 2011/August 3, 2012 A series of 2-(p-substituted-benzyl)-5[[4-(p-chloro/fluoro-phenyl)piperazin-1-yl]acetamido]-benzoxazoles were synthesized in need of new compounds for the fight against microbial pathogens. Their structures were elucidated by spectral techniques. These new derivatives, along with previously synthesized 2-(p-substituted-benzyl)-5-substituted-benzoxazoles, were evaluated for their antibacterial and antifungal activities against standard strains and drug-resistant isolates in comparison with ampicillin, gentamicin sulfate, ofloxacin, vancomycin, fluconazole, and amphotericin B trihydrate. The minimum inhibitory concentration (MIC) of each compound was determined by a two-fold serial dilution technique. The compounds were found to possess a broad spectrum of antimicrobial activities with MIC values of 32-256 mu g/ml. Although standard drugs were more active against the pathogenes employed in this study, the activities of the new benzoxazoles and reference drugs against drug-resistant isolates of the microorganisms were largely similar.
引用
收藏
页码:466 / 472
页数:7
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