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阿尔茨海默病多靶点导向配体的可持续药物发现。

Sustainable Drug Discovery of Multi-Target-Directed Ligands for Alzheimer's Disease.

机构信息

Department of Pharmacy and Biotechnology, Alma Mater Studiorum - University of Bologna, Via Belmeloro 6, 40126 Bologna, Italy.

Department for Life Quality Studies, Alma Mater Studiorum - University of Bologna, Corso d'Augusto 237, 47921 Rimini, Italy.

出版信息

J Med Chem. 2021 Apr 22;64(8):4972-4990. doi: 10.1021/acs.jmedchem.1c00048. Epub 2021 Apr 8.

Abstract

The multifactorial nature of Alzheimer's disease (AD) is a reason for the lack of effective drugs as well as a basis for the development of "multi-target-directed ligands" (MTDLs). As cases increase in developing countries, there is a need of new drugs that are not only effective but also accessible. With this motivation, we report the first sustainable MTDLs, derived from cashew nutshell liquid (CNSL), an inexpensive food waste with anti-inflammatory properties. We applied a framework combination of functionalized CNSL components and well-established acetylcholinesterase (AChE)/butyrylcholinesterase (BChE) tacrine templates. MTDLs were selected based on hepatic, neuronal, and microglial cell toxicity. Enzymatic studies disclosed potent and selective AChE/BChE inhibitors (, , and ), with subnanomolar activities. The X-ray crystal structure of complexed with BChE allowed rationalizing the observed activity (0.0352 nM). Investigation in BV-2 microglial cells revealed antineuroinflammatory and neuroprotective activities for and (already at 0.01 μM), confirming the design rationale.

摘要

阿尔茨海默病(AD)的多因素性质是缺乏有效药物的原因,也是开发“多靶点定向配体”(MTDL)的基础。随着发展中国家病例的增加,人们需要不仅有效而且可及的新药。基于这一动机,我们报告了第一个源自腰果壳液(CNSL)的可持续 MTDL,CNSL 是一种具有抗炎特性的廉价食品废物。我们应用了功能化 CNSL 成分和成熟的乙酰胆碱酯酶(AChE)/丁酰胆碱酯酶(BChE)他克林模板的组合框架。根据肝、神经元和小胶质细胞毒性选择 MTDL。酶研究揭示了具有强大和选择性的 AChE/BChE 抑制剂(、和),其活性达到亚纳摩尔水平。与 BChE 复合的 X 射线晶体结构允许合理化观察到的活性(0.0352 nM)。在 BV-2 小胶质细胞中的研究显示了 和 (在 0.01 μM 时已经如此)的抗神经炎症和神经保护活性,证实了设计原理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17d5/8154578/b7570c5a9d00/jm1c00048_0002.jpg

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