Oxazolomycins: Natural product lead structures for novel antibacterials by click fragment conjugation

被引:21
作者
Bagwell, Claire L. [1 ]
Moloney, Mark G. [1 ]
Yaqoob, Muhammad [1 ]
机构
[1] Univ Oxford, Dept Chem, Chem Res Lab, Oxford OX1 3TA, England
基金
英国工程与自然科学研究理事会;
关键词
Antibacterials; Natural products; Click conjugation; DIASTEREOCONTROLLED SYNTHESIS; TETRAMIC ACIDS; DRUGS; CHEMISTRY; DISCOVERY; COMPOUND; PYROGLUTAMATES; BIOSYNTHESIS; CURROMYCIN; INHIBITOR;
D O I
10.1016/j.bmcl.2010.02.066
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Conjugation of amide and lactam subunits by a 'Click' type approach provides access to structural mimics of the oxazolomycin series of natural products, some of which exhibit antibacterial activity. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2090 / 2094
页数:5
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