Design, synthesis and antimicrobial evaluation of novel benzoxazole derivatives

被引:49
|
作者
Zhang, Wei [1 ,2 ]
Liu, Jingbao [1 ]
Macho, Jocelyn M. [2 ]
Jiang, Xizhen [1 ]
Xie, Dongsheng [1 ]
Jiang, Faqin [1 ]
Liu, Wenlu [1 ]
Fu, Lei [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Pharm, 800 Dongchuan Rd, Shanghai 200240, Peoples R China
[2] Univ Florida, Dept Chem, Gainesville, FL 32611 USA
关键词
Antibacterial activity; Minimum inhibitory concentration; Benzoxazole; Propanoic acid; ACID-ESTER DERIVATIVES; TYROSINE-PHOSPHATASE; 1B; MICROBIOLOGICAL ACTIVITY; BENZAZOLE DERIVATIVES; TOPOISOMERASE-II; INHIBITORS; BENZOTHIAZOLES; BENZIMIDAZOLES; ANALOGS; A23187;
D O I
10.1016/j.ejmech.2016.10.010
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The synthesis of (S)-2-(4-tert-butylphenoxy)-3-(benzoxazol-5-yl) propanoic acid derivatives (2a-k) were described and their in vitro antibacterial activities were determined against Gram-negative and -positive bacteria. These compounds were found to exert a broad spectrum of activity against the screened bacteria, but poor MIC values were found for Candida albicans fungi. Compound 2b bearing a hydrophobic aromatic tie was the most active derivative against all bacteria studied with MIC values ranging from 0.098 to 0.78 mu g/mL. The activity of 2b against B. subtilis was 2-fold higher than Penicillin, and 8-to 510-fold higher than other control antibiotics. (C) 2016 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:7 / 14
页数:8
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