Biomedical Research Centre, University Hospital Hradec Kralove, Sokolska 581, 500 05 Hradec Kralove, Czech Republic.
National Institute of Mental Health, Topolova 748, 250 67 Klecany, Czech Republic.
Curr Alzheimer Res. 2019;16(9):772-800. doi: 10.2174/1567205016666190228122956.
Alzheimer's Disease (AD) is a neurodegenerative disorder with an increasing impact on society. Because currently available therapy has only a short-term effect, a huge number of novel compounds are developed every year exploiting knowledge of the various aspects of AD pathophysiology. To better address the pathological complexity of AD, one of the most extensively pursued strategies by medicinal chemists is based on Multi-target-directed Ligands (MTDLs). Donepezil is one of the currently approved drugs for AD therapy acting as an acetylcholinesterase inhibitor. In this review, we have made an extensive literature survey focusing on donepezil-derived MTDL hybrids primarily targeting on different levels cholinesterases and amyloid beta (Aβ) peptide. The targeting includes direct interaction of the compounds with Aβ, AChE-induced Aβ aggregation, inhibition of BACE-1 enzyme, and modulation of biometal balance thus impeding Aβ assembly.
阿尔茨海默病(AD)是一种神经退行性疾病,对社会的影响日益增加。由于目前可用的治疗方法只有短期效果,因此每年都会开发大量利用 AD 病理生理学各个方面知识的新型化合物。为了更好地解决 AD 的病理复杂性,药物化学家最广泛追求的策略之一是基于多靶点定向配体(MTDL)。多奈哌齐是目前批准用于 AD 治疗的药物之一,作为乙酰胆碱酯酶抑制剂。在这篇综述中,我们进行了广泛的文献调查,主要集中在多奈哌齐衍生的 MTDL 杂合药物上,这些药物主要针对不同水平的胆碱酯酶和淀粉样β(Aβ)肽。这些靶点包括化合物与 Aβ的直接相互作用、AChE 诱导的 Aβ聚集、BACE-1 酶抑制以及生物金属平衡的调节,从而阻止 Aβ组装。