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Procyanidins and Phlobatannins from the Twigs of Rosa multiflora and Their Neuroprotective Activity

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dc.contributor.authorLee, Tae Hyun-
dc.contributor.authorHong, Seong-Min-
dc.contributor.authorYoon, Da Hye-
dc.contributor.authorKim, Sun Yeou-
dc.contributor.authorKim, Chung Sub-
dc.contributor.authorLee, Kang Ro-
dc.date.accessioned2022-05-18T00:40:07Z-
dc.date.available2022-05-18T00:40:07Z-
dc.date.created2022-03-26-
dc.date.issued2022-04-
dc.identifier.issn0163-3864-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/84352-
dc.description.abstractThree new procyanidins (1-3), two new phlobatannins (6 and 7), a new flavan-3,4-diol glycoside (9), and a new neolignan glycoside (10), along with three previously reported compounds (4, 5, and 8) were isolated from the twigs of Rosa multiflora. The chemical structures of the new compounds (1-3, 6, 7, 9, and 10) were characterized by spectroscopic data interpretation, including NMR (1H and 13C NMR, 1H-1H COSY, HSQC, HMBC, and NOESY) and HRESIMS analysis. Experimental ECD data analysis was conducted to assign the absolute configurations of the new compounds (1-3, 6, 7, 9, and 10). The absolute configuration of the sugar moieties was verified through a chiral derivatization method and LC-MS analysis. All the isolated compounds (1-10) were evaluated for their anti-neuroinflammatory activity based on inhibitory effects on nitric oxide production using a lipopolysaccharide-stimulated murine microglia BV-2 cell line and for their neurotrophic effects on nerve growth factor induction in C6 glioma. © 2022 American Chemical Society and American Society of Pharmacognosy.-
dc.language영어-
dc.language.isoen-
dc.publisherAmerican Chemical Society-
dc.relation.isPartOfJournal of Natural Products-
dc.titleProcyanidins and Phlobatannins from the Twigs of Rosa multiflora and Their Neuroprotective Activity-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000791431400016-
dc.identifier.doi10.1021/acs.jnatprod.1c01033-
dc.identifier.bibliographicCitationJournal of Natural Products, v.85, no.4, pp.917 - 926-
dc.description.isOpenAccessN-
dc.identifier.scopusid2-s2.0-85126574160-
dc.citation.endPage926-
dc.citation.startPage917-
dc.citation.titleJournal of Natural Products-
dc.citation.volume85-
dc.citation.number4-
dc.contributor.affiliatedAuthorHong, Seong-Min-
dc.contributor.affiliatedAuthorYoon, Da Hye-
dc.contributor.affiliatedAuthorKim, Sun Yeou-
dc.type.docTypeArticle-
dc.subject.keywordPlusMAGNETIC-RESONANCE SPECTRA-
dc.subject.keywordPlusCONDENSED TANNINS-
dc.subject.keywordPlusROOTS-
dc.subject.keywordPlusLIGNANS-
dc.relation.journalResearchAreaPlant Sciences-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPlant Sciences-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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