Discovery of benzimidazole derivatives as modulators of mitochondrial function: A potential treatment for Alzheimer's disease

Authors
Kim, TaeHunYang, Ha YunPark, Beoung GunJung, Seo YunPark, Jong-HyunPark, Ki DukMin, Sun-JoonTae, JinsungYang, HyejinCho, SuengmokCho, Sung JinSong, HyundongMook-Jung, InheeLee, JiyounPae, Ae Nim
Issue Date
2017-01-05
Publisher
ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
Citation
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, v.125, pp.1172 - 1192
Abstract
In this study, we designed a library of compounds based on the structures of well-known ligands of the 18 kDa translocator protein (TSPO), one of the putative components of the mPTP. We performed diverse mitochondrial functional assays to assess their ability to restore cells from A beta-induced toxicity in vitro and in vivo. Among tested compounds, compound 25 effectively improved cognitive function in animal models of AD. Given the excellent in vitro and in vivo activity and a favorable pharmacokinetic profile of compound 25, we believe that it can serve as a promising lead compound for a potential treatment option for AD. (C) 2016 Elsevier Masson SAS. All rights reserved.
Keywords
PERMEABILITY TRANSITION PORE; AMYLOID-BETA; CYCLOPHILIN-D; A-BETA; INHIBITOR; TSPO; REPERFUSION; DYSFUNCTION; HYPOTHESIS; DIAGNOSIS; PERMEABILITY TRANSITION PORE; AMYLOID-BETA; CYCLOPHILIN-D; A-BETA; INHIBITOR; TSPO; REPERFUSION; DYSFUNCTION; HYPOTHESIS; DIAGNOSIS; Translocator protein; TSPO; Mitochondrial permeability transition pore; Alzheimer' s disease; Mitochondrial dysfunction; A beta
ISSN
0223-5234
URI
https://pubs.kist.re.kr/handle/201004/123219
DOI
10.1016/j.ejmech.2016.11.017
Appears in Collections:
KIST Article > 2017
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