Abstract
Tuberculosis (TB) is still a major health concern worldwide. The increasing incidences of multi-drug-resistant tuberculosis (MDR-TB) necessitate the development of new anti-TB drugs acting via novel mode of action. The search of newer drugs for TB led to the identification of several quinoline-based antimycobacterial agents against both the drug-sensitive and MDR-TB. These agents have been designed by substituting quinoline scaffold with diverse chemical functionalities as well as by modifying quinoline/quinolone-based antibacterial drugs. Several of quinoline/quinolone derivatives displayed excellent antimycobacterial activity and were found free of cytotoxicity. This review highlights the critical aspects of design and structure–activity relationship of quinoline- and quinolone-based antimycobacterial agents.
Acknowledgements
Authors thank Chairman, ISF College of Pharmacy, Moga (PB), India, for his valuable support and encouragement.
Declaration of interest
The authors have declared no conflict of interest.