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Chemical Constituents from the Roots and Rhizomes of Sophora tonkinensis and Their Effects on Proprotein Convertase Substilisin/Kexin Type 9 Expression

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dc.contributor.authorPel, Pisey-
dc.contributor.authorChae, Hee-Sung-
dc.contributor.authorNhoek, Piseth-
dc.contributor.authorKim, Young-Mi-
dc.contributor.authorAn, Chae-Yeong-
dc.contributor.authorYoo, Hunseung-
dc.contributor.authorKang, Minseok-
dc.contributor.authorKim, Hyun Woo-
dc.contributor.authorChoi, Young Hee-
dc.contributor.authorChin, Young-Won-
dc.date.accessioned2022-09-30T05:52:11Z-
dc.date.available2022-09-30T05:52:11Z-
dc.date.created2022-07-13-
dc.date.issued2022-06-
dc.identifier.citationACS Omega, Vol.7 No.24, pp.20952-20958-
dc.identifier.issn2470-1343-
dc.identifier.urihttps://hdl.handle.net/10371/184886-
dc.description.abstractThis study was conducted to further investigate bioactive molecules from Sophora tonkinensis that can inhibit proprotein convertase substilisin/kexin type 9 (PCSK9) expression. After interpreting NMR spectroscopic data and MS spectral data of all isolates, a new naturally occurring compound, 6-hydroxy-vitexin-2 ''-O-rhamnoside (7), was identified along with 30 known compounds. The calculation of the gauge-including atomic orbital (GAIO) and electronic circular dichroism (ECD) proposed the absolute configuration of 17 as (2S,3R)-methyl-2-(4-hydroxybenzyl)tartrate by comparing the calculated ECD with experimental data. All isolates were tested for their inhibitory effects on PCSK9 mRNA expression. Of the tested compounds, (+)-isolariciresinol (12) inhibited PCSK9 expression via down- ation of HNF1 alpha and SREBPs.-
dc.language영어-
dc.publisherAmerican Chemical Society-
dc.titleChemical Constituents from the Roots and Rhizomes of Sophora tonkinensis and Their Effects on Proprotein Convertase Substilisin/Kexin Type 9 Expression-
dc.typeArticle-
dc.identifier.doi10.1021/acsomega.2c01676-
dc.citation.journaltitleACS Omega-
dc.identifier.wosid000815335100001-
dc.identifier.scopusid2-s2.0-85133318175-
dc.citation.endpage20958-
dc.citation.number24-
dc.citation.startpage20952-
dc.citation.volume7-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorChin, Young-Won-
dc.type.docTypeArticle-
dc.description.journalClass1-
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