Suppr超能文献

喹唑啉衍生物治疗阿尔茨海默病的潜力:全面综述。

Therapeutic potential of quinazoline derivatives for Alzheimer's disease: A comprehensive review.

机构信息

Department of Chemistry, University of Louisiana at Lafayette, Lafayette, LA, 70504, USA.

Worcester Polytechnic Institute, 100 Institute Road, Worcester, MA, 01609, USA.

出版信息

Eur J Med Chem. 2022 Jan 5;227:113949. doi: 10.1016/j.ejmech.2021.113949. Epub 2021 Oct 27.

Abstract

Quinazolines are considered as a promising class of bioactive heterocyclic compounds with broad properties. Particularly, the quinazoline scaffold has an impressive role in the design and synthesis of new CNS-active drugs. The drug-like properties and pharmacological characteristics of quinazoline could lead to different drugs with various targets. Among CNS disorders, Alzheimer's disease (AD) is a progressive neurodegenerative disorder with memory loss, cognitive decline and language dysfunction. AD is a complex and multifactorial disease therefore, the need for finding multi-target drugs against this devastative disease is urgent. A literature survey revealed that quinazoline derivatives have diverse therapeutic potential for AD as modulators/inhibitors of β-amyloid, tau protein, cholinesterases, monoamine oxidases, and phosphodiesterases as well as other protective effects. Thus, we describe here the most relevant and recent studies about anti-AD agents with quinazoline structure which can further aid the development and discovery of new anti-AD agents.

摘要

喹唑啉被认为是一类具有广泛特性的很有前途的生物活性杂环化合物。特别是,喹唑啉支架在设计和合成新型中枢神经系统活性药物方面发挥了重要作用。喹唑啉的类药性和药理学特性可以导致针对不同靶点的不同药物。在中枢神经系统疾病中,阿尔茨海默病(AD)是一种进行性神经退行性疾病,伴有记忆丧失、认知能力下降和语言功能障碍。AD 是一种复杂的多因素疾病,因此,迫切需要寻找针对这种破坏性疾病的多靶标药物。文献调查显示,喹唑啉衍生物作为β-淀粉样蛋白、tau 蛋白、胆碱酯酶、单胺氧化酶和磷酸二酯酶的调节剂/抑制剂以及其他保护作用,具有治疗 AD 的多种潜在作用。因此,我们在这里描述了具有喹唑啉结构的最相关和最新的抗 AD 药物研究,这可以进一步帮助开发和发现新的抗 AD 药物。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验