Antimycobacterial activities of 5-alkyl (or halo)-3′-substituted pyrimidine nucleoside analogs

被引:14
作者
Srivastav, Naveen C. [1 ]
Shakya, Neeraj [1 ]
Bhavanam, Sudha [1 ]
Agrawal, Amogh [1 ]
Tse, Chris [1 ]
Desroches, Nancy [1 ]
Kunimoto, Dennis Y. [2 ]
Kumar, Rakesh [1 ]
机构
[1] Univ Alberta Hosp, Dept Lab Med & Pathol, Edmonton, AB T6G 2H7, Canada
[2] Univ Alberta, Fac Med & Dent, Dept Med, Edmonton, AB T6G 2H7, Canada
基金
加拿大健康研究院;
关键词
Tuberculosis; Pyrimidine nucleosides; MYCOBACTERIUM-TUBERCULOSIS; ANTIVIRAL ACTIVITY; RESISTANT; BOVIS; DEOXYRIBONUCLEOSIDES; 3'-AZIDO; STRAINS; HIV-1;
D O I
10.1016/j.bmcl.2011.11.114
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Several 5-alkyl (or halo)-3'-azido (amino or halo) analogs of pyrimidine nucleosides have been synthesized and evaluated against Mycobacterium bovis, Mycobacterium tuberculosis and Mycobacterium avium. Among these compounds, 3'-azido-5-ethyl-2',3'-dideoxyuridine (3) was found to have significant antimycobacterial activities against M. bovis (MIC50 = 1 mu g/mL), M. tuberculosis (MIC50 = 10 mu g/mL) and M. avium (MIC50 = 10 mu g/mL). (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1091 / 1094
页数:4
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