Synthesis, Characterization and Biological Evaluation of a Series of Levofloxacin Carboxamide Analogues
In present work an attempt was made to synthesize various analogues of levofloxacin by introducing new functionality at carboxylic group position via nucleophilic substitution reaction. For this purpose the carboxylic group at C-6 was esterified and later subjected to nucleophilic attack at the carb...
Saved in:
Published in | Bulletin of the Korean Chemical Society Vol. 30; no. 10; pp. 2294 - 2298 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
대한화학회
20.10.2009
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | In present work an attempt was made to synthesize various analogues of levofloxacin by introducing new functionality at carboxylic group position via nucleophilic substitution reaction. For this purpose the carboxylic group at C-6 was esterified and later subjected to nucleophilic attack at the carbonyl carbon by various aromatic amines. Structure of the analogues was confirmed by different techniques i.e. IR, 1H NMR and mass spectrometry. The antibacterial activity of the derivatives was also assessed and compared with the parent against a series of Gram-positive and Gramnegative bacteria. A synergistic as well as antagonistic behavior was observed in these derivatives. Additionally unlike levofloxacin, the derivatives were also found to modulate oxidative burst response of phagocytes exhibiting moderate to significant inhibitory activity. KCI Citation Count: 10 |
---|---|
Bibliography: | G704-000067.2009.30.10.017 |
ISSN: | 0253-2964 1229-5949 |
DOI: | 10.5012/bkcs.2009.30.10.2294 |