Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research, Raebareli, India.
Curr Drug Targets. 2022;23(9):933-953. doi: 10.2174/1389450123666220328153741.
Alzheimer's disease (AD) is an irreversible, progressive neurodegenerative disorder that may account for approximately 60-70% of cases of dementia worldwide. AD is characterized by impaired behavioural and cognitive functions, including memory, language, conception, attentiveness, judgment, and reasoning problems. The two important hallmarks of AD are the appearance of plaques and tangles of amyloid-beta (Aβ) and tau proteins, respectively, in the brain based on the etiology of the disease, including cholinergic impairment, metal dyshomeostasis, oxidative stress, and degradation of neurotransmitters. Currently, the used medication only provides alleviation of symptoms but is not effective in curing the disease, which creates the need to develop new molecules to treat AD. Heterocyclic compounds have proven their ability to be developed as drugs for the treatment of various diseases. The five-membered heterocyclic compound triazole has received foremost fascination for the discovery of new drugs due to the possibility of structural variation. Moreover, it has proved its significance in various drug categories. This review mainly summarizes the recent advancements in the development of novel 1,2,3-triazole and 1,2,4-triazole-based molecules in the drug discovery process for targeting various AD targets such as phosphodiesterase 1 (PDE1) inhibitors, apoptosis signal-regulating kinase 1 (ASK1) inhibitors, somatostatin receptor subtype-4 (SSTR4) agonist, several other druggable targets, molecular modelling studies, as well as various methodologies for the synthesis of triazoles containing molecules such as click reaction, Pellizzari reaction, and Einhorn- Brunner reaction.
阿尔茨海默病(AD)是一种不可逆转的、进行性的神经退行性疾病,可能占全球痴呆症病例的约 60-70%。AD 的特征是行为和认知功能受损,包括记忆、语言、概念、注意力、判断力和推理问题。AD 的两个重要标志是大脑中淀粉样β(Aβ)和tau 蛋白的斑块和缠结的出现,基于疾病的病因,包括胆碱能损伤、金属动态平衡紊乱、氧化应激和神经递质降解。目前,使用的药物仅能缓解症状,但不能有效治疗疾病,这就需要开发新的分子来治疗 AD。杂环化合物已被证明有能力开发成治疗各种疾病的药物。由于结构变化的可能性,五元杂环化合物三唑受到了开发新药的首要关注。此外,它已被证明在各种药物类别中具有重要意义。本文主要综述了近年来在药物发现过程中开发新型 1,2,3-三唑和 1,2,4-三唑类化合物的最新进展,这些化合物针对各种 AD 靶点,如磷酸二酯酶 1(PDE1)抑制剂、凋亡信号调节激酶 1(ASK1)抑制剂、生长抑素受体亚型-4(SSTR4)激动剂、其他几种可成药靶点、分子模拟研究以及含三唑分子的各种合成方法,如点击反应、Pellizzari 反应和 Einhorn-Brunner 反应。