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Isocoumarins and Benzoquinones with Their Proprotein Convertase Subtilisin/Kexin Type 9 Expression Inhibitory Activities from Dried Roots of Lysimachia vulgaris

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dc.contributor.authorPel, Pisey-
dc.contributor.authorKim, Young-Mi-
dc.contributor.authorKim, Hyun Ji-
dc.contributor.authorNhoek, Piseth-
dc.contributor.authorAn, Chae-Yeong-
dc.contributor.authorSon, Min-Gyung-
dc.contributor.authorWon, Hongic-
dc.contributor.authorLee, Seung Eun-
dc.contributor.authorLee, Jeonghoon-
dc.contributor.authorKim, Hyun Woo-
dc.contributor.authorChoi, Young Hee-
dc.contributor.authorLee, Chang Hoon-
dc.contributor.authorChin, Young-Won-
dc.date.accessioned2024-08-08T11:31:17Z-
dc.date.available2024-08-08T11:31:17Z-
dc.date.issued2022-12-
dc.identifier.issn2470-1343-
dc.identifier.issn2470-1343-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/21712-
dc.description.abstractA phytochemical investigation of the n-hexane-soluble chemical constituents of Lysimachia vulgaris roots allowed for selection using a proprotein convertase subtilisin-kexin type 9 (PCSK9) mRNA expression monitoring assay in HepG2 cells. This led to the isolation of two previously undescribed isocoumarins of natural origin, 8 ' Z,11 ' Z-octadecadienyl-6,8-dihydroxyisocoumarin (1) and 3-pentadecyl-6,8-dihydroxyisocoumarin (2), along with 20 previously reported compounds (3-22). All of the structures were established using NMR spectroscopic data and MS analysis. Of the isolates, 1 and 3 were found to inhibit PCSK9, inducible degrader of the low-density lipoprotein receptor (IDOL), and SREBP2 mRNA expression. Further computational dockings of both 1 and 3 to C-ring of IDOL E3 ubiquitin ligase predicted the mechanism behind the inhibitory effect of these compounds on the enzyme.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherAmerican Chemical Society-
dc.titleIsocoumarins and Benzoquinones with Their Proprotein Convertase Subtilisin/Kexin Type 9 Expression Inhibitory Activities from Dried Roots of Lysimachia vulgaris-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1021/acsomega.2c06660-
dc.identifier.scopusid2-s2.0-85143888955-
dc.identifier.wosid000894800300001-
dc.identifier.bibliographicCitationACS Omega, v.7, no.50, pp 47296 - 47305-
dc.citation.titleACS Omega-
dc.citation.volume7-
dc.citation.number50-
dc.citation.startPage47296-
dc.citation.endPage47305-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusCHEMICAL-CONSTITUENTS-
dc.subject.keywordPlusPCSK9-
dc.subject.keywordPlusACID-
dc.subject.keywordPlusIDOL-
dc.subject.keywordPlusDEGRADATION-
dc.subject.keywordPlusMETABOLISM-
dc.subject.keywordPlusOAKMOSS-
dc.subject.keywordPlusC-13-
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