氨基甲酸酯
喹啉
化学
体外
神经保护
铅化合物
组合化学
IC50型
药理学
立体化学
生物化学
有机化学
医学
作者
Hongsong Chen,Jing Mi,Sen Li,Zhengwei Liu,Jing Yang,Rui Chen,Yujie Wang,Yujuan Ban,Yi Zhou,Wu Dong,Zhipei Sang
标识
DOI:10.1080/14756366.2023.2169682
摘要
A series of novel quinoline-O-carbamate derivatives was rationally designed for treating Alzheimer's disease (AD) by multi-target-directed ligands (MTDLs) strategy. The target compounds were synthesised and evaluated by AChE/BuChE inhibition and anti-inflammatory property. The in vitro activities showed that compound 3f was a reversible dual eeAChE/eqBuChE inhibitor with IC50 values of 1.3 µM and 0.81 µM, respectively. Moreover, compound 3f displayed good anti-inflammatory property by decreasing the production of IL-6, IL-1β and NO. In addition, compound 3f presented significant neuroprotective effect on Aβ25-35-induced PC12 cell injury. Furthermore, compound 3f presented good stabilities in artificial gastrointestinal fluids, liver microsomes in vitro and plasma. Furthermore, compound 3f could improve AlCl3-induced zebrafish AD model by increasing the level of ACh. Therefore, compound 3f was a promising multifunctional agent for the treatment of AD.
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