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β-分泌酶酶 1(BACE1):阿尔茨海默病的生化之谜。

The β-Secretase Enzyme BACE1: A Biochemical Enigma for Alzheimer's Disease.

机构信息

Department of Pharmaceutical Chemistry, Parul Institute of Pharmacy, Parul University, Vadodara, Gujarat 391760, India.

Ramanbhai Patel College of Pharmacy, Charotar University of Science and Technology, Changa, Gujarat 388421, India.

出版信息

CNS Neurol Disord Drug Targets. 2020;19(3):184-194. doi: 10.2174/1871527319666200526144141.

Abstract

Beta site amyloid precursor protein cleaving enzyme 1 (BACE1) is a rational target in Alzheimer's Disease (AD) drug development due to its role in amyloidogenic cleavage of Amyloid Precursor Protein (APP) in generating Amyloid β (Aβ). This β-secretase cleaves not only Amyloid Precursor Protein (APP) and its homologues, but also small series of substrates including neuregulin and β subunit of voltage-gated sodium channel that play a very important role in the development and normal function of the brain. Moreover, BACE1 is modulated at the post-translational level by several factors that are associated with both physiological and pathological functions. Since the discovery of BACE1 over a decade ago, medicinal chemistry and pharmacokinetics of BACE1 small molecule inhibitors have proven challenging for the treatment of Alzheimer's disease.

摘要

β 位淀粉样前体蛋白水解酶 1(BACE1)在阿尔茨海默病(AD)药物开发中是一个合理的靶点,因为它在淀粉样蛋白生成β(Aβ)的淀粉样前体蛋白(APP)的淀粉样蛋白形成裂解中起作用。这种β-分泌酶不仅裂解淀粉样前体蛋白(APP)及其同源物,还裂解小系列的底物,包括神经调节蛋白和电压门控钠离子通道的β亚基,这些在大脑的发育和正常功能中起着非常重要的作用。此外,BACE1 在后翻译水平上受到与生理和病理功能相关的几种因素的调节。自从十多年前发现 BACE1 以来,BACE1 小分子抑制剂的药物化学和药代动力学一直是治疗阿尔茨海默病的挑战。

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