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A novel hybrid of 6-chlorotacrine and metal-amyloid-beta modulator for inhibition of acetylcholinesterase and metal-induced amyloid-beta aggregation

Author(s)
Kochi, AkikoEckroat, Todd J.Green, Keith D.Mayhoub, Abdelrahman S.Lim, Mi HeeGarneau-Tsodikova, Sylvie
Issued Date
2013-11
DOI
10.1039/c3sc51902c
URI
https://scholarworks.unist.ac.kr/handle/201301/8535
Fulltext
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84885085100
Citation
CHEMICAL SCIENCE, v.4, no.11, pp.4137 - 4145
Abstract
The number of people suffering from Alzheimer's disease (AD) is expected to increase dramatically in the coming decades. Currently, acetylcholinesterase inhibitors (AChEis) provide some relief of cognitive symptoms, while newer approaches, such as amyloid-β (Aβ)-targeted metal chelation, offer potential hope for slowing and/or reversing disease progression. This work details the synthesis and biochemical evaluation of a novel hybrid of 6-chlorotacrine and a metal-Aβ modulator that chemically combines an AChEi and an Aβ-targeted metal chelator into a single molecule. This hybrid shows potent inhibition of AChE under various conditions, interaction with Cu 2+ and Zn2+, control of metal-free and metal-induced Aβ aggregate assembly, and disaggregation of preformed metal-free and metal-associated Aβ aggregates. As such, the hybrid described herein represents a promising, new multifunctional compound for AD studies.
Publisher
ROYAL SOC CHEMISTRY
ISSN
2041-6520

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