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具有抗氧化活性的 BACE1 抑制剂的设计、合成及生物活性评价。

Design, synthesis, and biological activity evaluation of BACE1 inhibitors with antioxidant activity.

机构信息

Department of Medicinal Chemistry, Nanjing University of Chinese Medicine, Nanjing, China.

出版信息

Drug Dev Res. 2020 Apr;81(2):206-214. doi: 10.1002/ddr.21585. Epub 2019 Aug 9.

Abstract

The proteolytic enzyme β-secretase (BACE1) plays a central role in the synthesis of the pathogenic β-amyloid peptides (Aβ) in Alzheimer's disease (AD), antioxidants could attenuate the AD syndrome and prevent the disease progression. In this study, BACE1 inhibitors (D1-D18) with free radical-scavenging activities were synthesized by molecular hybridization of 2-aminopyridine with natural antioxidants. The biological activity evaluation showed that D1 had obvious inhibitory activity against BACE1, and strong antioxidant activity in 1,1-diphenyl-2-picrylhydrazyl (DPPH) and 2,2'-azinobis-(3-ethylbenzthiazoline-6-sulphonate) (ABTS ) assay, which could be used as a lead compound for further study.

摘要

β-分泌酶(BACE1)是阿尔茨海默病(AD)中致病β-淀粉样肽(Aβ)合成的关键酶,抗氧化剂可以减轻 AD 综合征并阻止疾病进展。在这项研究中,通过将 2-氨基吡啶与天然抗氧化剂进行分子杂交,合成了具有自由基清除活性的 BACE1 抑制剂(D1-D18)。生物活性评价表明,D1 对 BACE1 具有明显的抑制活性,并且在 1,1-二苯基-2-苦基肼(DPPH)和 2,2'-联氮双-(3-乙基苯并噻唑啉-6-磺酸)(ABTS)测定中具有很强的抗氧化活性,可作为进一步研究的先导化合物。

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