多奈哌齐
竞争对手
神经保护
发病机制
药理学
塔克林
疾病
医学
痴呆
水杨酸
乙酰胆碱酯酶
化学
生物化学
内科学
酶
作者
Yi Zhou,Ying He,Teng Xue,Jing Mi,Jing Yang,Rongrui Wei,Bo Liu,Qinge Ma,Zhenghuai Tan,Zhipei Sang
标识
DOI:10.1080/14756366.2023.2231661
摘要
Alzheimer’s disease (AD) is a chronic, progressive brain degenerative disease that is common in the elderly. So far, there is no effective treatment. The multi-target-directed ligands (MTDLs) strategy has been recognised as the most promising approach due to the complexity of the pathogenesis of AD. Herein, novel salicylic acid–donepezil–rivastigmine hybrids were designed and synthesised. The bioactivity results exhibited that 5a was a reversible and selective eqBChE inhibitor (IC50 = 0.53 μM), and the docking provided the possible mechanism. Compound 5a also displayed potential anti-inflammatory effects and significant neuroprotective effect. Moreover, 5a exhibited favourable stabilities in artificial gastrointestinal solution and plasma. Finally, 5a demonstrated potential cognitive improvement in scopolamine-induced cognitive dysfunction. Hence, 5a was a potential multifunctional lead compound against AD.
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