Gulcan Hayrettin Ozan, Kosar Muberra
Faculty of Pharmacy, Eastern Mediterranean University, Famagusta, T.R. North Cyprus, via Mersin 10 Turkey.
Curr Top Med Chem. 2022 Mar 4;22(5):395-407. doi: 10.2174/1568026621666211111153626.
The strategies to combat Alzheimer's Disease (AD) have been changing with respect to the failures of many drug candidates assessed in clinical studies, the complex pathophysiology of AD, and the limitations of the current drugs employed. So far, none of the targets, either validated or nonvalidated, have been shown to be purely causative in the generation and development of AD. Considering the progressive and the neurodegenerative characteristics of the disease, the main strategy has been based on the design of molecules capable of showing activity on more than one receptor, and it is defined as multi-target ligand design strategy. The hybrid molecule concept is an outcome of this approach. Donepezil, as one of the currently employed drugs for AD therapy, has also been utilized in hybrid drug design studies. This review has aimed to present the promising donepezil-like hybrid molecules introduced in the recent period. Particularly, multi-target ligands with additional activities concomitant to cholinesterase inhibition are preferred.
鉴于在临床研究中评估的许多候选药物的失败、阿尔茨海默病(AD)复杂的病理生理学以及当前所用药物的局限性,对抗AD的策略一直在不断变化。到目前为止,无论是已验证的还是未经验证的靶点,都未被证明在AD的发生和发展中是纯粹的病因。考虑到该疾病的进行性和神经退行性特征,主要策略基于设计能够对多种受体显示活性的分子,这被定义为多靶点配体设计策略。杂合分子概念就是这种方法的产物。多奈哌齐作为目前用于AD治疗的药物之一,也已被用于杂合药物设计研究。本综述旨在介绍近期引入的有前景的多奈哌齐样杂合分子。特别地,优先选择具有伴随胆碱酯酶抑制的额外活性的多靶点配体。