Piperazinyl-linked fluoroquinolone dimers possessing potent antibacterial activity against drug-resistant strains of Staphylococcus aureus
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Published on: March 2, 2020
Robert J Kerns1, Michael J Rybak, Glenn W Kaatz
1Division of Medicinal and Natural Products Chemistry, The University of Iowa, Iowa City 52242, USA. robert-kerns@uiowa.edu
Abstract:
The synthesis of symmetric and asymmetric piperazinyl-linked dimers of the fluoroquinolone class of antibiotics is described. Specific dimers are shown to possess potent antibacterial activity against drug-resistant strains of Staphylococcus aureus, including strains possessing resistance due to the NorA multidrug efflux pump and a mutation in the quinolone resistance-determining region of topoisomerase IV.
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