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dc.citation.conferencePlace KO -
dc.citation.title 119회 대한화학회 춘계학술대회 -
dc.contributor.author 이혁진 -
dc.contributor.author 임미희 -
dc.date.accessioned 2023-12-19T19:09:16Z -
dc.date.available 2023-12-19T19:09:16Z -
dc.date.created 2017-04-17 -
dc.date.issued 2017-04-20 -
dc.description.abstract To elucidate the involvement of individual and inter-related pathological factors [i.e., amyloid-β (Aβ), metals, and oxidative stress] in the pathogenesis of Alzheimer’s disease (AD), chemical tools have been developed. Characteristics required for such tool construction, however, have not been clearly identified; thus, the optimization of available tools or new design has been limited. In this presentation, we will present key structural properties and mechanisms that can determine tools’ regulatory reactivities with multiple pathogenic features found in AD. A series of small molecules was built up through rational structural selection and variations onto the framework of a tool useful for in vitro and in vivo metal–Aβ investigation. Variations include: (i) location and number of an Aβ interacting moiety; (ii) metal binding site; and (iii) denticity and structural flexibility. Detailed biochemical, biophysical, and computational studies were able to provide a foundation of how to originate molecular formulas to devise chemical tools capable of controlling the reactivities of various pathological components through distinct mechanisms. Overall, our multidisciplinary investigation illustrates that a structure-mechanism-based strategy can assist in significantly advancing the rational tool invention for such a complicated brain disease. -
dc.identifier.bibliographicCitation 119회 대한화학회 춘계학술대회 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/39775 -
dc.language 영어 -
dc.publisher 119회 대한화학회 춘계학술대회 -
dc.title Structural and Mechanistic Insights into Development of Chemical Tools to Control Individual and Inter-Related Pathological Features in Alzheimer’s Disease -
dc.type Conference Paper -
dc.date.conferenceDate 2017-04-19 -

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