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dc.contributor.authorYu, Jae Sik-
dc.contributor.authorLee, Dahae-
dc.contributor.authorLee, Seoung Rak-
dc.contributor.authorLee, Jae Wook-
dc.contributor.authorChoi, Chang-Ik-
dc.contributor.authorJang, Tae Su-
dc.contributor.authorKang, Ki Sung-
dc.contributor.authorKim, Ki Hyun-
dc.date.accessioned2024-01-19T23:31:56Z-
dc.date.available2024-01-19T23:31:56Z-
dc.date.created2021-09-03-
dc.date.issued2018-02-
dc.identifier.issn0045-2068-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/121742-
dc.description.abstractThe fruit of the white mulberry tree (Morus alba L.) is a multiple fruit with a sweet flavor commonly consumed around the world. Chemical investigation of the fruits led to the isolation of two indole acetic acid derivatives (1-2) including a new compound, which turned out to be an isolation artifact, 3S-(beta-D-gluco pyranosyloxy)-2,3-dihydro-2-oxo-1H-indole-3-acetic acid butyl ester (1), along with five known compounds (3-7). Compounds 2 and 7 were newly identified from mulberry fruit. The new isolation artifact (1) exhibited cytotoxic effect on human cervical cancer Hela cells in a dose-dependent manner. Compound 1 activated caspase-8, caspase-9, and caspase-3, followed by cleavage of PARP, a substrate of caspase-3, in a dose-dependent manner. Simultaneous alterations in protein expression of mitochondrial factors Bax, BID and Bcl-2 were also observed. A comparison between compounds 1 and 2 led to a structure-activity relationship analysis of the cytotoxic effect. These results suggest that compound 1 could be beneficial in human cervical cancer treatment, and provide a theoretical basis for further application of compound 1. (C) 2017 Elsevier Inc. All rights reserved.-
dc.languageEnglish-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.subjectAPOPTOSIS INDUCTION-
dc.subjectCISPLATIN-
dc.subjectACCUMULATION-
dc.subjectACTIVATION-
dc.subjectRESISTANCE-
dc.subjectCASPASE-3-
dc.subjectDESIGN-
dc.subjectLEAVES-
dc.subjectCELLS-
dc.subjectBCL-2-
dc.titleChemical characterization of cytotoxic indole acetic acid derivative from mulberry fruit (Morus alba L.) against human cervical cancer-
dc.typeArticle-
dc.identifier.doi10.1016/j.bioorg.2017.10.015-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBIOORGANIC CHEMISTRY, v.76, pp.28 - 36-
dc.citation.titleBIOORGANIC CHEMISTRY-
dc.citation.volume76-
dc.citation.startPage28-
dc.citation.endPage36-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000425897800004-
dc.identifier.scopusid2-s2.0-85032796899-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusAPOPTOSIS INDUCTION-
dc.subject.keywordPlusCISPLATIN-
dc.subject.keywordPlusACCUMULATION-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusRESISTANCE-
dc.subject.keywordPlusCASPASE-3-
dc.subject.keywordPlusDESIGN-
dc.subject.keywordPlusLEAVES-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusBCL-2-
dc.subject.keywordAuthorMulberry-
dc.subject.keywordAuthorMorus alba-
dc.subject.keywordAuthorIndole acetic acid-
dc.subject.keywordAuthorHuman cervical cancer-
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