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Kapic S.,Glaxosmithkline | Kapic S.,Galagos Research Center Ltd. | Fajdetic A.,Glaxosmithkline | Fajdetic A.,Galagos Research Center Ltd. | And 11 more authors.
Bioorganic and Medicinal Chemistry | Year: 2011

A set of novel macrolones containing the flexible C8 basic linker and quinolone 3-(2′-hydroxyethyl)carboxamido group has been prepared and structurally characterized by NMR and IR spectroscopy, mass spectrometry and molecular modeling. The new compounds were evaluated in vitro against a panel of erythromycin-susceptible and erythromycin-resistant Gram-positive and Gram-negative bacterial strains. Compared to azithromycin, most of the compounds exhibited improved in vitro potency against the key respiratory pathogens. © 2011 Elsevier Ltd. All rights reserved.

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