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Lignans from Saururus chinensis with Inhibitory Effects on Nitric Oxide Production

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dc.contributor.authorJin, Qinghao-
dc.contributor.authorLee, Jin Woo-
dc.contributor.authorKim, Jun Gu-
dc.contributor.authorLee, Dongho-
dc.contributor.authorHong, Jin Tae-
dc.contributor.authorKim, Youngsoo-
dc.contributor.authorLee, Mi Kyeong-
dc.contributor.authorHwang, Bang Yeon-
dc.date.accessioned2021-09-01T01:15:37Z-
dc.date.available2021-09-01T01:15:37Z-
dc.date.created2021-06-19-
dc.date.issued2019-11-
dc.identifier.issn0163-3864-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/62005-
dc.description.abstractThree biogenetically related ent-sauchinone-type lignans (1-3), four 8-O-4'-type neolignans (4-7), a diaryldimethylbutane lignan (8), and a cyclic carbonate (9), along with 12 known compounds, have been isolated from a methanol extract of the aerial parts of Saururus chinensis. The structures of the new compounds (1-9) were determined by analysis of their 1D and 2D NMR spectra, HRESIMS, and ECD data. A putative biosynthetic pathway for the three ents-auchinone-type lignans (1-3) was postulated. Compounds 1, 7, and 10 showed inhibitory effects on LPS-induced NO production in RAW 264.7 cells with IC50 values of 5.6, 8.6, and 9.2 mu M, respectively.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherAMER CHEMICAL SOC-
dc.subjectTRANSACTIVATION ACTIVITY-
dc.subjectANTIOXIDANT ACTIVITIES-
dc.subjectSECONDARY METABOLITES-
dc.subjectSESQUILIGNANS-
dc.subjectSAUCHINONE-
dc.subjectNEOLIGNAN-
dc.subjectROOTS-
dc.titleLignans from Saururus chinensis with Inhibitory Effects on Nitric Oxide Production-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Dongho-
dc.identifier.doi10.1021/acs.jnatprod.9b00520-
dc.identifier.scopusid2-s2.0-85074281653-
dc.identifier.wosid000499741400010-
dc.identifier.bibliographicCitationJOURNAL OF NATURAL PRODUCTS, v.82, no.11, pp.3002 - 3009-
dc.relation.isPartOfJOURNAL OF NATURAL PRODUCTS-
dc.citation.titleJOURNAL OF NATURAL PRODUCTS-
dc.citation.volume82-
dc.citation.number11-
dc.citation.startPage3002-
dc.citation.endPage3009-
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.keywordPlusTRANSACTIVATION ACTIVITY-
dc.subject.keywordPlusANTIOXIDANT ACTIVITIES-
dc.subject.keywordPlusSECONDARY METABOLITES-
dc.subject.keywordPlusSESQUILIGNANS-
dc.subject.keywordPlusSAUCHINONE-
dc.subject.keywordPlusNEOLIGNAN-
dc.subject.keywordPlusROOTS-
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