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dc.contributor.authorPark, Jae Sung-
dc.contributor.authorKo, Keebeom-
dc.contributor.authorKim, Seong-Hwan-
dc.contributor.authorLee, Jae Kyun-
dc.contributor.authorPark, Jin-Soo-
dc.contributor.authorPark, Keunwan-
dc.contributor.authorKim, Mi Ri-
dc.contributor.authorKang, Kyungsu-
dc.contributor.authorOh, Dong-Chan-
dc.contributor.authorKim, Sun Yeou-
dc.contributor.authorYumnam, Silvia-
dc.contributor.authorKwon, Hak Cheol-
dc.contributor.authorShin, Jongheon-
dc.date.accessioned2024-01-19T14:03:44Z-
dc.date.available2024-01-19T14:03:44Z-
dc.date.created2021-10-21-
dc.date.issued2021-07-23-
dc.identifier.issn0163-3864-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/116680-
dc.description.abstractThe tropolone-bearing sesquiterpenes juniperone A (1) and norjuniperone A (2) were isolated from the folk medicinal plant Juniperus chinensis, and their structures were determined by a combination of spectroscopic and crystallographic methods. Photojuniperones A1 (3) and A2 (4), bearing bicyclo[3,2,0]heptadienones derived from tropolone, were photochemically produced and structurally identified by spectroscopic methods. Predicted by the machine learning-based assay, 1 significantly inhibited the action of tyrosinase. The new compounds also inhibited lipid accumulation and enhanced the extracellular glycerol excretion.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.subjectPAPER CHROMATOGRAPHY-
dc.subjectPHOTOELECTROCYCLIZATION-
dc.subjectPHOTOCYCLIZATION-
dc.subjectCONFINEMENT-
dc.subjectHINOKITIOL-
dc.subjectINHIBITORS-
dc.subjectINDUCTION-
dc.titleTropolone-Bearing Sesquiterpenes from Juniperus chinensis: Structures, Photochemistry and Bioactivity-
dc.typeArticle-
dc.identifier.doi10.1021/acs.jnatprod.1c00321-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF NATURAL PRODUCTS, v.84, no.7, pp.2020 - 2027-
dc.citation.titleJOURNAL OF NATURAL PRODUCTS-
dc.citation.volume84-
dc.citation.number7-
dc.citation.startPage2020-
dc.citation.endPage2027-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000677582700017-
dc.identifier.scopusid2-s2.0-85110978409-
dc.relation.journalWebOfScienceCategoryPlant Sciences-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalResearchAreaPlant Sciences-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.type.docTypeArticle-
dc.subject.keywordPlusPAPER CHROMATOGRAPHY-
dc.subject.keywordPlusPHOTOELECTROCYCLIZATION-
dc.subject.keywordPlusPHOTOCYCLIZATION-
dc.subject.keywordPlusCONFINEMENT-
dc.subject.keywordPlusHINOKITIOL-
dc.subject.keywordPlusINHIBITORS-
dc.subject.keywordPlusINDUCTION-
dc.subject.keywordAuthorTropolone-
dc.subject.keywordAuthorSesquiterpene-
dc.subject.keywordAuthorJuniperus chinensis-
dc.subject.keywordAuthorPhotochemistry-
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