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dc.contributor.authorPark, Cheon-Soo-
dc.contributor.authorAhn, Yongchel-
dc.contributor.authorLee, Dahae-
dc.contributor.authorMoon, Sung Won-
dc.contributor.authorKim, Ki Hyun-
dc.contributor.authorYamabe, Noriko-
dc.contributor.authorHwang, Gwi Seo-
dc.contributor.authorJang, Hyuk Jai-
dc.contributor.authorLee, Heesu-
dc.contributor.authorKang, Ki Sung-
dc.contributor.authorLee, Jae Wook-
dc.date.accessioned2024-01-20T05:31:02Z-
dc.date.available2024-01-20T05:31:02Z-
dc.date.created2021-09-03-
dc.date.issued2015-12-15-
dc.identifier.issn0960-894X-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/124622-
dc.description.abstractEight chalcone analogues were prepared and evaluated for their cytotoxic effects in human hepatoma HepG2 cells. Compound 5 had a potent cytotoxic effect. The percentage of apoptotic cells was significantly higher in compound 5-treated cells than in control cells. Exposure to compound 5 for 24 h induced cleavage of caspase-8 and -3, and poly (ADP-ribose) polymerase (PARP). Our findings suggest that compound 5 is the active chalcone analogue that contributes to cell death in HepG2 cells via the extrinsic apoptotic pathway. (C) 2015 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPergamon Press Ltd.-
dc.subjectBIOLOGICAL EVALUATION-
dc.subjectDERIVATIVES-
dc.titleSynthesis of apoptotic chalcone analogues in HepG2 human hepatocellular carcinoma cells-
dc.typeArticle-
dc.identifier.doi10.1016/j.bmcl.2015.10.093-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBioorganic & Medicinal Chemistry Letters, v.25, no.24, pp.5705 - 5707-
dc.citation.titleBioorganic & Medicinal Chemistry Letters-
dc.citation.volume25-
dc.citation.number24-
dc.citation.startPage5705-
dc.citation.endPage5707-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000365032800009-
dc.identifier.scopusid2-s2.0-84947280056-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusBIOLOGICAL EVALUATION-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordAuthorChalcone-
dc.subject.keywordAuthorAnticancer-
dc.subject.keywordAuthorHepG2-
dc.subject.keywordAuthorApoptosis-
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KIST Article > 2015
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