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Synthesis and evaluation of oxime derivatives as modulators for amyloid beta-induced mitochondrial dysfunction

Authors
Kim, Young SeubJung, Sun HwaPark, Beoung-GeonKo, Min KyungJang, Hyun-SeoChoi, KihangBaik, Ja-HyunLee, JiyounLee, Jae KyunPae, Ae NimCho, Yong SeoMin, Sun-Joon
Issue Date
Apr-2013
Publisher
Elsevier BV
Keywords
Alzheimer's disease; Mitochondrial permeability transition pore (mPTP); Oxime derivatives; Amyloid beta; Pharmacokinetics
Citation
European Journal of Medicinal Chemistry, v.62, pp 71 - 83
Pages
13
Indexed
SCI
SCIE
SCOPUS
Journal Title
European Journal of Medicinal Chemistry
Volume
62
Start Page
71
End Page
83
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/28459
DOI
10.1016/j.ejmech.2012.12.033
ISSN
0223-5234
1768-3254
Abstract
Starting from quinuclidinyl oxime 1 identified by preliminary screening, a series of azacycles-containing oxime derivatives was synthesized. Their mPTP blocking activities were evaluated by a JC-1 assay, measuring the change of mitochondrial membrane potential. The inhibitory activity of nine compounds against amyloid beta-induced mPTP opening was comparable or even superior to that of piracetam. Among them, 12d effectively maintained mitochondrial function and cell viabilities on the ATP assay, the MTT assay, and the ROS assay. In addition, it exhibited favorable in vitro stability and pharmacokinetic characteristics, which hold a promise for further development of AD therapeutics. (C) 2012 Elsevier Masson SAS. All rights reserved.
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ERICA 공학대학 (ERICA 에너지바이오학과)
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