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光致变色假不可逆丁酰胆碱酯酶抑制剂可实现抑制的光学控制,并可在照射后恢复阿尔茨海默病小鼠模型的认知功能。

Photoswitchable Pseudoirreversible Butyrylcholinesterase Inhibitors Allow Optical Control of Inhibition and Enable Restoration of Cognition in an Alzheimer's Disease Mouse Model upon Irradiation.

机构信息

Pharmaceutical and Medicinal Chemistry, Institute of Pharmacy and Food Chemistry, Julius-Maximilian-Universität Würzburg, Am Hubland, 97074, Würzburg, Germany.

MMDN, University of Montpellier, INSERM, EPHE, 34095 Montpellier, France.

出版信息

J Am Chem Soc. 2022 Feb 23;144(7):3279-3284. doi: 10.1021/jacs.1c13492. Epub 2022 Feb 9.

Abstract

To develop tools to investigate the biological functions of butyrylcholinesterase (BChE) and the mechanisms by which BChE affects Alzheimer's disease (AD), we synthesized several selective, nanomolar active, pseudoirreversible photoswitchable BChE inhibitors. The compounds were able to specifically influence different kinetic parameters of the inhibition process by light. For one compound, a 10-fold difference in the IC-values (44.6 nM , 424 nM ) was translated to an "all or nothing" response with complete recovery in a murine cognition-deficit AD model at dosages as low as 0.3 mg/kg.

摘要

为了开发研究丁酰胆碱酯酶(BChE)的生物学功能以及 BChE 影响阿尔茨海默病(AD)的机制的工具,我们合成了几种选择性的、纳摩尔级活性的、假不可逆的光可切换的 BChE 抑制剂。这些化合物能够通过光照特异性地影响抑制过程的不同动力学参数。对于一种化合物,IC 值(44.6 nM ,424 nM)的 10 倍差异转化为一种“全有或全无”的反应,在低至 0.3 毫克/千克剂量的小鼠认知缺陷 AD 模型中完全恢复。

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