Multiple reactivities of flavonoids towards pathological elements in Alzheimer's disease: Structure-activity relationship
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Geewoo Nam | - |
dc.contributor.author | Mannkyu Hong | - |
dc.contributor.author | Juri Lee | - |
dc.contributor.author | Hyuck Jin Lee | - |
dc.contributor.author | Yonghwan Ji | - |
dc.contributor.author | Juhye Kang | - |
dc.contributor.author | Mu-Hyun Baik | - |
dc.contributor.author | Mi Hee Lim | - |
dc.date.accessioned | 2020-12-22T02:32:30Z | - |
dc.date.accessioned | 2020-12-22T02:32:30Z | - |
dc.date.available | 2020-12-22T02:32:30Z | - |
dc.date.available | 2020-12-22T02:32:30Z | - |
dc.date.created | 2020-11-09 | - |
dc.date.issued | 2020-10 | - |
dc.identifier.issn | 2041-6520 | - |
dc.identifier.uri | https://pr.ibs.re.kr/handle/8788114/7601 | - |
dc.description.abstract | © The Royal Society of Chemistry.Amyloid-β (Aβ) accumulation, metal ion dyshomeostasis, oxidative stress, and cholinergic deficit are four major characteristics of Alzheimer's disease (AD). Herein, we report the reactivities of 12 flavonoids against four pathogenic elements of AD: metal-free and metal-bound Aβ, free radicals, and acetylcholinesterase. A series of 12 flavonoids was selected based on the molecular structures that are responsible for multiple reactivities including hydroxyl substitution and transfer of the B ring from C2 to C3. Our experimental and computational studies reveal that the catechol moiety, the hydroxyl groups at C3 and C7, and the position of the B ring are important for instilling multiple functions in flavonoids. We establish a structure-activity relationship of flavonoids that should be useful for designing chemical reagents with multiple reactivities against the pathological factors of AD. This journal i | - |
dc.description.uri | 1 | - |
dc.language | 영어 | - |
dc.publisher | ROYAL SOC CHEMISTRY | - |
dc.title | Multiple reactivities of flavonoids towards pathological elements in Alzheimer's disease: Structure-activity relationship | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.identifier.wosid | 000573713500023 | - |
dc.identifier.scopusid | 2-s2.0-85092235875 | - |
dc.identifier.rimsid | 73289 | - |
dc.contributor.affiliatedAuthor | Mannkyu Hong | - |
dc.contributor.affiliatedAuthor | Mu-Hyun Baik | - |
dc.identifier.doi | 10.1039/d0sc02046j | - |
dc.identifier.bibliographicCitation | CHEMICAL SCIENCE, v.11, no.37, pp.10243 - 10254 | - |
dc.citation.title | CHEMICAL SCIENCE | - |
dc.citation.volume | 11 | - |
dc.citation.number | 37 | - |
dc.citation.startPage | 10243 | - |
dc.citation.endPage | 10254 | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.subject.keywordPlus | AMYLOID-BETA PEPTIDE | - |
dc.subject.keywordPlus | ANTIOXIDANT ACTIVITY | - |
dc.subject.keywordPlus | CHOLINERGIC HYPOTHESIS | - |
dc.subject.keywordPlus | MOLECULAR-DYNAMICS | - |
dc.subject.keywordPlus | OXIDATIVE STRESS | - |
dc.subject.keywordPlus | AGGREGATION | - |
dc.subject.keywordPlus | MODULATION | - |
dc.subject.keywordPlus | CHEMISTRY | - |
dc.subject.keywordPlus | DESIGN | - |
dc.subject.keywordPlus | TOOL | - |