| Literature DB >> 12951115 |
Constantine G Boojamra1, Rémy C Lemoine, Johanne Blais, Nicole G Vernier, Karin A Stein, Angela Magon, Suzanne Chamberland, Scott J Hecker, Ving J Lee.
Abstract
Dihydropacidamycins having an antibacterial spectrum modified from that of the natural product pacidamycins and mureidomycins have been synthesized. Synthetic dihydropacidamycins with noteworthy antibacterial activity against wild-type and resistant Escherichia coli have been identified (MIC=4-8 microg/mL). Some dihydropacidamycins are shown to have activity against multi-resistant clinical strains of Mycobacterium tuberculosis. Compounds of this class are inhibitors of the cell wall biosynthetic enzyme, MraY.Entities:
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Year: 2003 PMID: 12951115 DOI: 10.1016/s0960-894x(03)00682-6
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823