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Inhibition of melanin production and tyrosinase expression of ergosterol derivatives from Phellinus pini

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dc.contributor.authorHong Y.J.-
dc.contributor.authorJang A.R.-
dc.contributor.authorYang K.S.-
dc.date.available2021-02-22T10:55:27Z-
dc.date.issued2013-09-
dc.identifier.issn1226-3907-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/6297-
dc.description.abstractThree ergosterol derivatives, ergosta-4,6,8(14),22-tetraen-3-one (1), ergosta-7,24(28)-dien-3-ol (2), and 5,8-epidioxyergosta-6,22-dien-3-ol(3) were isolated from the fruit body of Phellinus pini. Their structures were based on spectroscopic methods including IR, MS, and NMR (1D and 2D). These compounds were evaluated for their activity to decrease melanin production in α-MSH (melanocyte stimulating hormone) activated B16F10 cells. Compound 1, 2, and 3 reduced melanin content in a dose-dependent manner at concentrations of 5~15 uM. They also suppressed the tyrosinase expression of protein and m-RNA level dose dependently by western blot analysis and RT-PCR experiment in B16F10 murine melanoma cells.-
dc.format.extent5-
dc.language영어-
dc.language.isoENG-
dc.publisher한국생약학회-
dc.titleInhibition of melanin production and tyrosinase expression of ergosterol derivatives from Phellinus pini-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.scopusid2-s2.0-84887806870-
dc.identifier.bibliographicCitationNatural Product Sciences, v.19, no.3, pp 258 - 262-
dc.citation.titleNatural Product Sciences-
dc.citation.volume19-
dc.citation.number3-
dc.citation.startPage258-
dc.citation.endPage262-
dc.type.docTypeArticle-
dc.identifier.kciidART001804693-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.subject.keywordPlus5,8 epidioxyergosta 6,22 dien 3 ol-
dc.subject.keywordPlusalpha intermedin-
dc.subject.keywordPlusergosta 4,6,8(14),22 tetraen 3 one-
dc.subject.keywordPlusergosta 7,24(28) dien 3 ol-
dc.subject.keywordPlusergosterol-
dc.subject.keywordPlusmelanin-
dc.subject.keywordPlusmessenger RNA-
dc.subject.keywordPlusmonophenol monooxygenase-
dc.subject.keywordPlusunclassified drug-
dc.subject.keywordPlusanimal cell-
dc.subject.keywordPlusarticle-
dc.subject.keywordPlusconcentration (parameters)-
dc.subject.keywordPluscontrolled study-
dc.subject.keywordPlusdrug activity-
dc.subject.keywordPlusdrug isolation-
dc.subject.keywordPlusdrug structure-
dc.subject.keywordPlusenzyme activity-
dc.subject.keywordPlusfungal cell-
dc.subject.keywordPlusinfrared spectrometry-
dc.subject.keywordPlusmass spectrometry-
dc.subject.keywordPlusmelanogenesis-
dc.subject.keywordPlusmelanoma cell-
dc.subject.keywordPlusnonhuman-
dc.subject.keywordPlusnuclear magnetic resonance spectroscopy-
dc.subject.keywordPlusPhellinus-
dc.subject.keywordPlusPhellinus pini-
dc.subject.keywordPlusprotein expression-
dc.subject.keywordPlusprotein synthesis inhibition-
dc.subject.keywordPlusreal time polymerase chain reaction-
dc.subject.keywordPlusWestern blotting-
dc.subject.keywordAuthorB16F10 cells-
dc.subject.keywordAuthorErgosterol derivatives-
dc.subject.keywordAuthorMelanin content-
dc.subject.keywordAuthorPhellinus pini-
dc.subject.keywordAuthorTyrosinase-
dc.identifier.urlhttp://kiss.kstudy.com/thesis/thesis-view.asp?key=3177218-
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