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dc.contributor.author민선준-
dc.date.accessioned2018-05-29T05:19:15Z-
dc.date.available2018-05-29T05:19:15Z-
dc.date.issued2017-01-
dc.identifier.citationEUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, v. 125, Page. 1172-1192en_US
dc.identifier.issn0223-5234-
dc.identifier.issn1768-3254-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0223523416309552-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/71621-
dc.description.abstractIn 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.en_US
dc.description.sponsorshipThis work was supported by the National Research Council of Science & Technology (NST) grant by the Korea government (MSIP) (No. CRC-15-04-KIST) and KIST institutional program (2E26650). J.L. was supported by the Sungshin Women's University Research Grant of 2015-2-21-007.en_US
dc.language.isoen_USen_US
dc.publisherELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIERen_US
dc.subjectTranslocator proteinen_US
dc.subjectTSPOen_US
dc.subjectMitochondrial permeability transition poreen_US
dc.subjectAlzheimer's diseaseen_US
dc.subjectMitochondrial dysfunctionen_US
dc.subjectA betaen_US
dc.subjectPERMEABILITY TRANSITION POREen_US
dc.subjectAMYLOID-BETAen_US
dc.subjectCYCLOSPORINE-Aen_US
dc.subjectCYCLOPHILIN-Den_US
dc.subjectBRAIN-INJURYen_US
dc.subjectMOUSE MODELen_US
dc.subjectDYSFUNCTIONen_US
dc.subjectINHIBITORen_US
dc.subjectTSPOen_US
dc.subjectREPERFUSIONen_US
dc.titleDiscovery of benzimidazole derivatives as modulators of mitochondrial function: A potential treatment for Alzheimer's diseaseen_US
dc.typeArticleen_US
dc.relation.volume125-
dc.identifier.doi10.1016/j.ejmech.2016.11.017-
dc.relation.page1172-1192-
dc.relation.journalEUROPEAN JOURNAL OF MEDICINAL CHEMISTRY-
dc.contributor.googleauthorKim, TaeHun-
dc.contributor.googleauthorYang, Ha Yun-
dc.contributor.googleauthorPark, Beoung Gun-
dc.contributor.googleauthorJung, Seo Yun-
dc.contributor.googleauthorPark, Jong-Hyun-
dc.contributor.googleauthorPark, Ki Duk-
dc.contributor.googleauthorMin, Sun-Joon-
dc.contributor.googleauthorTae, Jinsung-
dc.contributor.googleauthorYang, Hyejin-
dc.contributor.googleauthorCho, Suengmok-
dc.contributor.googleauthorCho, Sung Jin-
dc.contributor.googleauthorSong, Hyundong-
dc.contributor.googleauthorMook-Jung, Inhee-
dc.contributor.googleauthorLee, Jiyoun-
dc.contributor.googleauthorPae, Ae Nim-
dc.relation.code2017000237-
dc.sector.campusE-
dc.sector.daehakCOLLEGE OF SCIENCE AND CONVERGENCE TECHNOLOGY[E]-
dc.sector.departmentDEPARTMENT OF CHEMICAL AND MOLECULAR ENGINEERING-
dc.identifier.pidsjmin-


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