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Furanocoumarins from the Roots of Angelica dahurica with Inhibitory Activity against Intracellular Reactive Oxygen Species Accumulation

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dc.contributor.authorKang, Unwoo-
dc.contributor.authorHan, Ah-Reum-
dc.contributor.authorSo, Yangkang-
dc.contributor.authorJin, Chang Hyun-
dc.contributor.authorRyu, Seung Mok-
dc.contributor.authorLee, Dongho-
dc.contributor.authorSeo, Eun Kyoung-
dc.date.accessioned2021-09-01T07:24:38Z-
dc.date.available2021-09-01T07:24:38Z-
dc.date.created2021-06-18-
dc.date.issued2019-09-
dc.identifier.issn0163-3864-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/63022-
dc.description.abstractFive new furanocoumarins, dahuribirin H (1), dahuribirin I (2), (2'S)-(+)-5-(2'-hydroxy-3'-methylbut-3'enyloxy)-8-(3 ''-methylbut-2 ''-enyloxy)psoralen (3), (2'R)(+)-5-(2',3'-epoxy-3'-methylbutoxy)-8-(3"-methylbut-2 ''- enyloxy)psoralen (4), and 5-methoxy-8((Z)-4'-(3 ''-methylbutanoate)-3'-methylbut-2'-enyloxy)psoralen (5), along with 15 known compounds (6-20), were isolated from the roots of Angelica dahurica. The structures of the new compounds were elucidated by spectroscopic analysis, along with electronic circular dichroism calculations and Mosher ester analysis. Compounds 3, 4, 11, 13, and 16 reduced H2O2-induced cell death in HepG2 cells and attenuated reactive oxygen species (ROS) formation without showing cytotoxicity, suggesting that these compounds might have cytoprotective effects against H2O2-induced oxidative damage via ROS scavenging activities.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherAMER CHEMICAL SOC-
dc.subjectLINEAR FURANOCOUMARINS-
dc.subjectOXIDATIVE STRESS-
dc.subjectIMPERATORIN-
dc.subjectCOUMARINS-
dc.subjectCONSTITUENTS-
dc.subjectIDENTIFICATION-
dc.subjectCELLS-
dc.subjectHERB-
dc.titleFuranocoumarins from the Roots of Angelica dahurica with Inhibitory Activity against Intracellular Reactive Oxygen Species Accumulation-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Dongho-
dc.identifier.doi10.1021/acs.patprod.9b00547-
dc.identifier.scopusid2-s2.0-85072584967-
dc.identifier.wosid000488424000028-
dc.identifier.bibliographicCitationJOURNAL OF NATURAL PRODUCTS, v.82, no.9, pp.2601 - 2607-
dc.relation.isPartOfJOURNAL OF NATURAL PRODUCTS-
dc.citation.titleJOURNAL OF NATURAL PRODUCTS-
dc.citation.volume82-
dc.citation.number9-
dc.citation.startPage2601-
dc.citation.endPage2607-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPlant Sciences-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPlant Sciences-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusLINEAR FURANOCOUMARINS-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusIMPERATORIN-
dc.subject.keywordPlusCOUMARINS-
dc.subject.keywordPlusCONSTITUENTS-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusHERB-
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