期刊
ACS MEDICINAL CHEMISTRY LETTERS
卷 3, 期 12, 页码 1013-1018出版社
AMER CHEMICAL SOC
DOI: 10.1021/ml300230h
关键词
total synthesis; ketolide antibiotics; antibiotic resistance; telithromycin; molecular modeling; desmethyl analogues
资金
- NIH [AI080968, GM070855]
- University of Maryland Computer-Aided Drug Design Center
There is an urgent need for novel sources of antibiotics to address the incessant and inevitable onset of bacterial resistance. To this end, we have initiated a structure-based drug design program that features a desmethylation strategy (i.e., replacing methyl groups with hydrogens). Herein, we report the total synthesis, molecular modeling, and biological evaluation of 4,8-didesmethyl telithromycin (5), a novel desmethyl analogue of the third-generation ketolide antibiotic telithromycin (2), which is an FDA-approved semisynthetic derivative of erythromycin (1). We found 5 to be eight times more active than previously prepared 4,8,10-tridesmethyl congener (3) and two times more active than 4,10-didesmethyl regioisomer (4) in MIC assays. While less potent than telithromycin (2) and paralleling the observations made in the previous study of 4,10-didesmethyl analogue (4), the inclusion of a single methyl group improves biological activity, thus supporting its role in antibiotic activity.
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