Desmethyl Macrolides: Synthesis and Evaluation of 4,8-Didesmethyl Telithromycin

作者：Wagh Bharat; Paul Tapas; Glassford Ian; DeBrosse Charles; Klepacki Dorota; Small Meagan C; MacKerell Alexander D Jr; Andrade Rodrigo B^*

来源：ACS Medicinal Chemistry Letters, 2012, 3(12): 1013-1018.

DOI：10.1021/ml300230h

• total synthesis
• ketolide antibiotics
• antibiotic resistance
• telithromycin
• molecular modeling
• desmethyl analogues

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.

• 出版日期2012-12