Journal of Heterocyclic Chemistry p. 1561 - 1568 (1994)
Update date:2022-08-17
Topics:
Ruxer
Lachoux
Ousset
Torregrosa
Mattioda
A few aza analogues of the quinolones have been prepared in the two milies of the 1,4-dihydro-4-oxopyridazino[1,6-a]indole-3-carboxylic acids and the 1,4-dihydro-4-oxopyrido[3',2':4,5]pyrrolo[1,2-b]pyridazine-3-carboxyli c acids to check their antibacterial potential. One compound 6c shows antibacterial activities of the level of nalidixic acid and represents a new lead structure differing from the classical quinolones.
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