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NO inhibitory constituents as potential anti-neuroinflammatory agents for AD from Blumea balsamifera

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dc.contributor.authorMa, Jun-
dc.contributor.authorRen, Quanhui-
dc.contributor.authorDong, Bangjian-
dc.contributor.authorShi, Zhaoyu-
dc.contributor.authorZhang, Jie-
dc.contributor.authorJin, Da-Qing-
dc.contributor.authorXu, Jing-
dc.contributor.authorOhizumi, Yasushi-
dc.contributor.authorLee, Dongho-
dc.contributor.authorGuo, Yuanqiang-
dc.date.accessioned2021-09-02T15:08:38Z-
dc.date.available2021-09-02T15:08:38Z-
dc.date.created2021-06-16-
dc.date.issued2018-02-
dc.identifier.issn0045-2068-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/77426-
dc.description.abstractOur continuous search for new nitric oxide (NO) inhibitory substances as anti-neuroinflammatory agents for AD resulted in the isolation of one new labdane diterpenoid and three new guaiane sesquiterpenoids, as well as ten known compounds from Blumea balsamifera. Their structures were elucidated by NMR spectroscopic data analysis and the time-dependent density functional theory (TDDFT) electronic circular dichroism (ECD) calculations. The anti-neuroinflammatory effects were examined by inhibiting NO release in LPS-induced murine microglial BV-2 cells. The possible mechanism of NO inhibition of some bioactive compounds was also investigated using molecular docking, which revealed the interactions of bioactive compounds with the iNOS protein. (C) 2017 Elsevier Inc. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.subjectALZHEIMERS-DISEASE-
dc.subjectANTICANCER ACTIVITIES-
dc.subjectINOS PROTEIN-
dc.subjectTRITERPENOIDS-
dc.subjectDITERPENOIDS-
dc.subjectFLAVONOIDS-
dc.subjectEXTRACTS-
dc.subjectCELLS-
dc.subjectEPIDEMIOLOGY-
dc.subjectMETABOLITES-
dc.titleNO inhibitory constituents as potential anti-neuroinflammatory agents for AD from Blumea balsamifera-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Dongho-
dc.identifier.doi10.1016/j.bioorg.2017.12.008-
dc.identifier.scopusid2-s2.0-85038834506-
dc.identifier.wosid000425897800047-
dc.identifier.bibliographicCitationBIOORGANIC CHEMISTRY, v.76, pp.449 - 457-
dc.relation.isPartOfBIOORGANIC CHEMISTRY-
dc.citation.titleBIOORGANIC CHEMISTRY-
dc.citation.volume76-
dc.citation.startPage449-
dc.citation.endPage457-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusALZHEIMERS-DISEASE-
dc.subject.keywordPlusANTICANCER ACTIVITIES-
dc.subject.keywordPlusINOS PROTEIN-
dc.subject.keywordPlusTRITERPENOIDS-
dc.subject.keywordPlusDITERPENOIDS-
dc.subject.keywordPlusFLAVONOIDS-
dc.subject.keywordPlusEXTRACTS-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusEPIDEMIOLOGY-
dc.subject.keywordPlusMETABOLITES-
dc.subject.keywordAuthorBlumea balsamifera-
dc.subject.keywordAuthorSesquiterpenoids-
dc.subject.keywordAuthorDiterpenoids-
dc.subject.keywordAuthorNO inhibitory activities-
dc.subject.keywordAuthorMolecular docking-
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