Exploring Quinazoline as a Scaffold for Developing Novel Therapeutics in Alzheimer's Disease

被引:1
作者
Abualassal, Qais [1 ]
Abudayeh, Zead [1 ]
Sirhan, Ala' [2 ]
Mkia, Abdulrahman [3 ]
机构
[1] Isra Univ, Fac Pharm, Dept Appl Pharmaceut Sci, Clin Pharm, Queen Alia Int Airport St, Amman 11622, Jordan
[2] Amman Arab Univ, Fac Pharm, Dept Pharm, Amman 11953, Jordan
[3] Al Ahliyya Amman Univ, Fac Allied Med Sci, Dept Biotechnol, Amman 19328, Jordan
关键词
quinazoline; Alzheimer's disease; drug discovery; cholinergic hypothesis; beta-amyloid hypothesis; DERIVATIVES; DESIGN; DEHYDROEVODIAMINE; INHIBITORS; DISCOVERY; DOCKING; DRUGS;
D O I
10.3390/molecules30030555
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Quinazoline, a privileged scaffold in medicinal chemistry, offers promising potential in the synthesis of anti-Alzheimer's disease (AD) drugs. This heterocyclic compound, characterized by its fused benzene and pyrimidine rings, enables the design of multifunctional agents targeting AD pathology. The drug-like aspects and pharmaceutical features of quinazoline derivatives have the potential to give rise to various therapeutic drugs. AD is a progressive neurodegenerative condition marked by memory decline, cognitive deterioration, and language disorders. Given its complexity and multifaceted nature, there is a pressing need to discover multi-target drugs to effectively address this debilitating disorder. A comprehensive literature review has demonstrated that quinazoline derivatives exhibit a wide range of therapeutic potential for AD. These compounds function as inhibitors of cholinesterases, beta-amyloid aggregation, oxidative stress, and tau protein, among other protective effects. Here, we highlight the most significant and recent research on quinazoline-based anti-AD agents, aiming to support the development and discovery of novel treatments for AD.
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页数:12
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