Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13302
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dc.contributor.authorMcCloskey S.
dc.contributor.authorNoppawan S.
dc.contributor.authorMongkolthanaruk W.
dc.contributor.authorSuwannasai N.
dc.contributor.authorSenawong T.
dc.contributor.authorPrawat U.
dc.date.accessioned2021-04-05T03:23:10Z-
dc.date.available2021-04-05T03:23:10Z-
dc.date.issued2017
dc.identifier.issn14786419
dc.identifier.other2-s2.0-84996542648
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/13302-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84996542648&doi=10.1080%2f14786419.2016.1258559&partnerID=40&md5=70e8da85d65dfa72ab59cc68ed02ae0e
dc.description.abstractA new cerebroside, namely allantoside (1), and 10 known compounds (2–11) were isolated from Xylaria allantoidea SWUF76. The structure of compound 1 was determined by comprehensive spectroscopic analysis including 1D and 2D nuclear magnetic resonance (NMR) as well as high-resolution electron ionisation mass spectrometry (HREIMS) and electrospray ionisation mass spectrometry (ESIMS). Compounds 1, 4, 5, 6, 7, 8 and 11 were evaluated for cytotoxic activities against cancer cell lines (Hela, HT29, HCT116 and MCF-7) and normal Vero cell lines by MTT assay. Compounds 6 and 7 exhibited anticancer activity after 24 h of treatment. Compound 7 showed significant cytotoxicity against Hela (IC50 = 2.24 μg/mL), HT29 (IC50 = 2.51 μg/mL), HCT116 (IC50 = 3.50 μg/mL) and MCF-7 (IC50 = 3.77 μg/mL) and Vero (IC50:3.65 μg/mL) cells. Compound 6 showed slight cytotoxicity against all tested cancer cell lines. © 2016 Informa UK Limited, trading as Taylor & Francis Group.
dc.subject3beta,5alpha dihydroxyergosta 7,22 dien 6 one
dc.subject5 hydroxymethylfurfural
dc.subjectallantoside
dc.subjectcerebroside
dc.subjectchaxine C
dc.subjectcytotoxic agent
dc.subjectergosterol
dc.subjectergosterol epoxide
dc.subjectfungal extract
dc.subjectmethylcholesta 7,22 diene 3beta,5alpha,6beta triol
dc.subjectn [10 (13,14 methylenedioxyphenyl) )pentadienoyl]pyrrolidine
dc.subjectnorincisterol A3
dc.subjectpiperazine derivative
dc.subjectunclassified drug
dc.subjectveratryl alcohol
dc.subjectantineoplastic agent
dc.subjectcerebroside
dc.subjectantineoplastic activity
dc.subjectArticle
dc.subjectAscomycetes
dc.subjectcarbon nuclear magnetic resonance
dc.subjectdrug cytotoxicity
dc.subjectdrug isolation
dc.subjectdrug structure
dc.subjectelectrospray mass spectrometry
dc.subjectHCT 116 cell line
dc.subjectHeLa cell line
dc.subjectheteronuclear multiple bond correlation
dc.subjectHT-29 cell line
dc.subjecthuman
dc.subjecthuman cell
dc.subjectIC50
dc.subjectinfrared spectroscopy
dc.subjectMCF-7 cell line
dc.subjectMTT assay
dc.subjectproton nuclear magnetic resonance
dc.subjectstereochemistry
dc.subjectVero cell line
dc.subjectXylaria allantoidea
dc.subjectchemistry
dc.subjectfermentation
dc.subjectisolation and purification
dc.subjectmetabolism
dc.subjectnuclear magnetic resonance spectroscopy
dc.subjecttumor cell line
dc.subjectXylariales
dc.subjectAntineoplastic Agents
dc.subjectCell Line, Tumor
dc.subjectCerebrosides
dc.subjectFermentation
dc.subjectHumans
dc.subjectMagnetic Resonance Spectroscopy
dc.subjectXylariales
dc.titleA new cerebroside and the cytotoxic constituents isolated from Xylaria allantoidea SWUF76
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationNatural Product Research. Vol 31, No.12 (2017), p.1422-1430
dc.identifier.doi10.1080/14786419.2016.1258559
Appears in Collections:Scopus 1983-2021

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