化学
加兰他明
竞争对手
美金刚
多奈哌齐
神经保护
乙酰胆碱酯酶
痴呆
药理学
NMDA受体
疾病
胆碱酯酶
体内
阿尔茨海默病
人口
神经科学
受体
内科学
生物化学
酶
心理学
生物
医学
生物技术
环境卫生
作者
Chandni Pathak,Uma D. Kabra
标识
DOI:10.1016/j.bioorg.2024.107152
摘要
Alzheimer’s disease (AD) is the most common form of dementia affecting specifically older population. AD is an irreversible neurodegenerative CNS disorder associated with complex pathophysiology. Presently, the USFDA has approved only four drugs viz. Donepezil, Rivastigmine, Memantine, and Galantamine for the treatment of AD. These drugs exhibit their neuroprotective effects either by inhibiting cholinesterase enzyme (ChE) or N-methyl-d-aspartate (NMDA) receptor. However, the conventional therapy “one target, one molecule” has failed to provide promising therapeutic effects due to the multifactorial nature of AD. This triggered the development of a novel strategy called Multi-Target Directed Ligand (MTDL) which involved designing one molecule that acts on multiple targets simultaneously. The present review discusses the detailed pathology involved in AD and the various MTDL design strategies bearing different heterocycles, in vitro and in vivo activities of the compounds, and their corresponding structure–activity relationships. This knowledge will allow us to identify and design more effective MTDLs for the treatment of AD.
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