Synthesis and diverse biological activity profile of triethylammonium isatin-3-hydrazones.

A series of biorelevant triethylammonium isatin hydrazones containing various substituents in the aromatic fragment have been synthesized. Their structure and composition were confirmed by NMR- and IR-spectroscopies, mass-spectrometry and elemental analysis. It was found that some representatives show activity against and higher or at the level of norfloxacin, including methicillin-resistant strains.