Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5218166 | Tetrahedron | 2012 | 8 Pages |
Abstract
The glmS riboswitch is a ribozyme found in numerous Gram-positive bacteria and responds to the cellular concentrations of glucosamine 6-phosphate (GlcN6P). Given the importance of GlcN6P for cell wall biosynthesis, the glmS riboswitch has become a new drug target for the development of antibiotics. Herein, we describe the efficient synthesis of three GlcN6P analogues and their evaluation on inducing self-cleavage of the glmS riboswitch from Bacillus subtilis. Our results provide valuable information for further elucidation of the structure-activity relationships and drug design for glmS riboswitch antibiotics.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Guan-Nan Wang, Pui Sai Lau, Yingfu Li, Xin-Shan Ye,