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Isolation and identification of an anticancer compound from the bark of Acer tegmentosum Maxim

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dc.contributor.authorKwon, Hyuck-Ju-
dc.contributor.authorKim, Yon-Suk-
dc.contributor.authorHwang, Jin-Woo-
dc.contributor.authorKim, Chul Young-
dc.contributor.authorLee, Sang-Hoon-
dc.contributor.authorMoon, Sang-Ho-
dc.contributor.authorJeon, Byong-Tae-
dc.contributor.authorPark, Pyo-Jam-
dc.date.accessioned2021-06-23T01:23:48Z-
dc.date.available2021-06-23T01:23:48Z-
dc.date.created2021-01-22-
dc.date.issued2014-07-
dc.identifier.issn1359-5113-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/25450-
dc.description.abstractIn this study, we investigated the anticancer activity of a newly isolated compound from Acer tegmentosum Maxim (ATM) in HepG2 cells. This compound was isolated by reverse-phase high-performance liquid chromatography (RP-HPLC) in a butanol-soluble fraction, which was shown to have the strongest anticancer activity. The isolated compound was identified as salidroside using multiple nuclear magnetic resonance (NMR) techniques, including 1H, 13C, correlated spectroscopy (COSY), heteronuclear single quantum coherence (HSQC), and heteronuclear multiple bond correlation (HMBC), as well as electrospray ionization mass spectroscopy (ESI/MS). The activity of salidroside was evaluated in HepG2 cells by analyzing cell proliferation, cell cycle distribution, Hoechst 33342 staining, and Western blots of apoptotic regulatory proteins. The results show that salidroside, an anticancer compound from ATM, exhibits strong apoptotic activity in HepG2 cells. Therefore, ATM extracts could be used as chemotherapeutic agent to induce apoptosis in hepatoblastoma cells. © 2014 Elsevier Ltd.-
dc.language영어-
dc.language.isoen-
dc.publisherElsevier BV-
dc.titleIsolation and identification of an anticancer compound from the bark of Acer tegmentosum Maxim-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Chul Young-
dc.identifier.doi10.1016/j.procbio.2014.03.002-
dc.identifier.scopusid2-s2.0-84899942481-
dc.identifier.wosid000337658700015-
dc.identifier.bibliographicCitationProcess Biochemistry, v.49, no.6, pp.1032 - 1039-
dc.relation.isPartOfProcess Biochemistry-
dc.citation.titleProcess Biochemistry-
dc.citation.volume49-
dc.citation.number6-
dc.citation.startPage1032-
dc.citation.endPage1039-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.subject.keywordPlusCell death-
dc.subject.keywordPlusCell proliferation-
dc.subject.keywordPlusElectrospray ionization-
dc.subject.keywordPlusHigh performance liquid chromatography-
dc.subject.keywordPlusMass spectrometry-
dc.subject.keywordPlusQuantum theory-
dc.subject.keywordPlusAcer tegmentosum Maxim-
dc.subject.keywordPlusAnticancer-
dc.subject.keywordPlusElectrospray ionization mass spectroscopy-
dc.subject.keywordPlusHep-g2 cells-
dc.subject.keywordPlusHetero-nuclear multiple bond correlations-
dc.subject.keywordPlusHeteronuclear single-quantum coherences-
dc.subject.keywordPlusReverse phase high-performance liquid chromatography-
dc.subject.keywordPlusSalidroside-
dc.subject.keywordPlusNuclear magnetic resonance spectroscopy-
dc.subject.keywordPlusAcer-
dc.subject.keywordPlusAcer tegmentosum-
dc.subject.keywordAuthorAcer tegmentosum Maxim-
dc.subject.keywordAuthorAnticancer-
dc.subject.keywordAuthorHepG2 cells-
dc.subject.keywordAuthorSalidroside-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S1359511314001342?via%3Dihub-
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