| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1394384 | European Journal of Medicinal Chemistry | 2013 | 10 Pages |
A series of 9-O-(3-aryl-2-propargyl)oxime ketolides 8 was synthesized and evaluated for in vitro antibacterial activity. Among 8, 8b–8d, and 8h–8l displayed dramatically improved potency against inducibly MLSB-resistant and efflux-resistant pathogens as compared to clarithromycin and azithromycin. Especially, 8i (Ar4-isoquinolyl) possessed an MIC of 0.064 μg/mL against constitutively MLSB-resistant Streptococcus pneumoniae, and MICs of 0.032–0.064 μg/mL against methicillin-resistant Staphylococcus aureus and methicillin-resistant Staphylococcus hominis. The analog 10 with a propyl linker was less effective than both the corresponding 8 and 9 containing propynyl and propenyl linkers. A docking study was performed to gain insight into the binding mode of series 8 and 9 and to rationalize the disparity found in the SAR of 8 and 9.
Graphical abstractThe extended aryl groups of 8i (purple), 9k (cyan) and cethromycin (green) interact with different rRNA pockets.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► A series of 9-O-(3-aryl-2-propargyl)oxime ketolides 8 was synthesized and evaluated. ► 8i was the best one with greatly enhanced potency against resistant pathogens. ► The sidechains of 8i and 9k bind to a different pocket from that of cethromycin. ► 10i and 10k were less effective than the corresponding 8i and 9k, respectively.
