化学
抗菌活性
加替沙星
部分
噻二唑类
细胞毒性
咪唑
立体化学
药物化学
组合化学
细菌
抗生素
左氧氟沙星
生物化学
体外
遗传学
生物
作者
Wenbo Xu,Meng Yuan,Jingxin Sun,Yuxuan Yang,Wan‐Xin Li,M.-Z. Wang,Ming‐Guan Piao,Siqi Li,Ji‐Shan Quan,Cheng Hua Jin
标识
DOI:10.1002/cbdv.202300105
摘要
A series of 2-cyclopropyl-5-(5-(6-methylpyridin-2-yl)-2-substituted-1H-imidazol-4-yl)-6-phenylimidazo[2,1-b][1,3,4]thiadiazoles (15a-t and 16a-f) were synthesized and their antibacterial activities were evaluated. More than half of the compounds showed moderate or strong antibacterial activity. Among them, compounds 15t (MIC=1-2 μg/mL) and 16d (MIC=0.5 μg/mL) showed the strongest antibacterial activities. Notably, compound 16d did not exhibit cytotoxicity in HepG2 cells and did not show hemolysis like the positive control compound Gatifloxacin. The results suggest that compound 16d should be further investigated as a candidate antibacterial agent.
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