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Salicinoyl Quinic Acids and Their Prostaglandin E-2 Production Inhibitory Activities from the Fruits of Casearia grewiifolia

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dc.contributor.authorNhoek, Piseth-
dc.contributor.authorAhn, Sungjin-
dc.contributor.authorPark, In Guk-
dc.contributor.authorPel, Pisey-
dc.contributor.authorHuh, Jungmoo-
dc.contributor.authorKim, Hyun Woo-
dc.contributor.authorAhn, Jongmin-
dc.contributor.authorKhiev, Piseth-
dc.contributor.authorChoi, Young Hee-
dc.contributor.authorLee, Kyeong-
dc.contributor.authorNoh, Minsoo-
dc.contributor.authorChin, Young-Won-
dc.date.accessioned2023-04-27T15:41:08Z-
dc.date.available2023-04-27T15:41:08Z-
dc.date.issued2021-09-24-
dc.identifier.issn0163-3864-
dc.identifier.issn1520-6025-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/4424-
dc.description.abstractPhytochemical investigation on the dried fruits of Casearia grewiifolia led to the identification of 10 new salicinoyl quinic acid derivatives (1-10), a new benzoyl quinic acid (11), and two known compounds (12 and 13). The structures of the new compounds were elucidated by interpreting 1D and 2D NMR spectroscopic data including HMBC and EXSIDE along with a chemical method for sugar unit analysis. All isolates were evaluated for their inhibitory activities against prostaglandin E-2 (PGE(2)) production in ultraviolet B (UVB)-irradiated HaCat keratinocytes. Of the isolates tested, compounds 6 and 12 were found to inhibit PGE(2) production with IC50 values of 20.5 and 28.8 mu M, respectively.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherAMER CHEMICAL SOC-
dc.titleSalicinoyl Quinic Acids and Their Prostaglandin E-2 Production Inhibitory Activities from the Fruits of Casearia grewiifolia-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1021/acs.jnatprod.1c00343-
dc.identifier.scopusid2-s2.0-85114857693-
dc.identifier.wosid000702066200004-
dc.identifier.bibliographicCitationJOURNAL OF NATURAL PRODUCTS, v.84, no.9, pp 2437 - 2446-
dc.citation.titleJOURNAL OF NATURAL PRODUCTS-
dc.citation.volume84-
dc.citation.number9-
dc.citation.startPage2437-
dc.citation.endPage2446-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
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.keywordPlusCYTOTOXIC CLERODANE DITERPENOIDS-
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