A series of pyridine chalcone derivatives were designed and synthesized, the structures were confirmed by 1HNMR, 13 CNMR and HRMS. In vitro biological activity evaluation results showed that compounds 5a, 5i, 5j, 5k, and 5m exhibited good biological activity against gram positive bacteria staphylococcus aureus (ATCC 29213). Further antibiotic activity of these five compounds against 11 clinical
... [Show full abstract] isolated methicillin-resistant staphylococcus aureus (MRSA) were evaluated. The results showed that the compounds 5a, 5j, 5k, and 5m exhibited good antibacterial activity against MRSA. Compound 5k showed the most effective activity
(minimum inhibitory concentration, MIC = 4 μg/mL). In terms of hemolytic activity evaluation, compound 5k
showed virtually no toxicity even in 1000 μg/mL concentration. To sum up, pyridine chalcone 5k was potential
for further antibiotic study as anti-MRSA agent.