Abstract
Two iminosugars have been designed and synthesized as potential inhibitors of UDP-Galf transferase, an enzyme involved in Mycobacterium tuberculosis cell wall biosynthesis. The design is based on a proposed model of the transition state for the transferase reaction. One of the two racemic compounds is the first reported inhibitor of the target enzyme from M. smegmatis.
Original language | English |
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Pages (from-to) | 2418-2420 |
Number of pages | 3 |
Journal | Organic and Biomolecular Chemistry |
Volume | 2 |
DOIs | |
Publication status | Published - 1 Jan 2004 |