Abstract

The introduction of quinolonic antimicrobials on the market caused a revolution in antibacterial therapy. 4-quinolone skeleton became the target of many studies of structure-activity relationship establishing the parameters considered optimal for the development of new quinolonic antibiotics. These parameters limited the development of new compounds, so it is possible finding compounds with changes in the same position with similar substituents. The purpose of this article is to identify quinolonic compounds which do not fit into one or more criteria determined as ideal in the structure-activity relationship studies for quinolonic antibiotics and exemplify that it is possible to develop of even more active compounds making changes in previously unalterable positions.

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