Design and synthesis of 1H-1,2,3-triazoles derived from econazole as antitubercular agents

被引:51
作者
Kim, Suhyun [1 ,2 ]
Cho, Sang-Nae [3 ,4 ]
Ohc, Taegwon [3 ,4 ]
Kim, Pilho [1 ]
机构
[1] Korea Res Inst Chem Technol, Canc & Infect Dis Therapeut Res Grp, Taejon 305606, South Korea
[2] Kyung Hee Univ, Coll Pharm, Seoul, South Korea
[3] Yonsei Univ, Coll Med, Dept Microbiol, Seoul 120749, South Korea
[4] Yonsei Univ, Coll Med, Inst Immunol & Immunol Dis, Seoul 120749, South Korea
基金
新加坡国家研究基金会;
关键词
Tuberculosis; Econazole; Triazole; Click chemistry; Microwave-assisted reactions; INHIBITORS; TUBERCULOSIS;
D O I
10.1016/j.bmcl.2012.09.041
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Econazole has been known to be active against Mycobacterium tuberculosis. We have designed and synthesized 1H-1,2,3-triazoles derived from econazole as antitubercular agents. The majority of triazole derivatives have been prepared by microwave-assisted click chemistry. It turned out that all of the prepared triazoles had no antifungal activities. However, most of the hydroxy-triazoles (6a and 10) apparently turned out to have antitubercular activities. Overall, hydroxy-triazoles 10 were more active than their corresponding ether-triazoles 11. While the MIC value of hydroxy-triazole 10d was as good as econazole (16 mu g/mL), the MIC value of 10a was two-fold more active than econazole, suggesting that this 1H-1,2,3-triazole scaffold (3) could be further optimized to develop Mtb specific agents. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6844 / 6847
页数:4
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