硫醚
缩醛
利奈唑啉
侧链
抗菌活性
酰胺
立体化学
化学
抗菌剂
细胞毒性
组合化学
有机化学
抗生素
体外
细菌
生物化学
生物
万古霉素
聚合物
金黄色葡萄球菌
遗传学
作者
Tian Zeng,Huahua Ren,Yao Zou,Yewei Sun,Xiaojian Jiang
标识
DOI:10.1002/slct.202401685
摘要
Abstract The modification on the C 5 ‐side chain in Linezolid analogues development is sporadic owing to the fact that trivial alternation on this position always leads to significant loss of antibacterial activity and in many cases to complete inactivity. The present work focused on constructing the potent yet relatively unexplored C 5 ‐side chain of Linezolid, therefore various C 5 ‐thioethers were synthesized and evaluated for their antibacterial activities. The most potent candidates, hydroxyl thioether ( R )‐ 5 a , ( R )‐ 10 a , and ( R )‐ 5 r which featuring a linear N,S ‐acetal amide motif at the C 5 side chain, shown strong antibacterial activities with no observable cytotoxicity.
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