摘要

A series of hybrid 4-aminoquinoline-1,3,5-triazine conjugates 7a-g were synthesized and evaluated for their in vitro antibacterial activity against several Gram-positive and Gram-negative micro-organisms. The entire set of target compounds displayed potent to excellent activity against human disease causing pathogens with reference to Levofloxacin as a standard drug.

  • 出版日期2012