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DC Field | Value | Language |
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dc.contributor.author | McCloskey S. | |
dc.contributor.author | Noppawan S. | |
dc.contributor.author | Mongkolthanaruk W. | |
dc.contributor.author | Suwannasai N. | |
dc.contributor.author | Senawong T. | |
dc.contributor.author | Prawat U. | |
dc.date.accessioned | 2021-04-05T03:23:10Z | - |
dc.date.available | 2021-04-05T03:23:10Z | - |
dc.date.issued | 2017 | |
dc.identifier.issn | 14786419 | |
dc.identifier.other | 2-s2.0-84996542648 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/13302 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84996542648&doi=10.1080%2f14786419.2016.1258559&partnerID=40&md5=70e8da85d65dfa72ab59cc68ed02ae0e | |
dc.description.abstract | A 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.subject | 3beta,5alpha dihydroxyergosta 7,22 dien 6 one | |
dc.subject | 5 hydroxymethylfurfural | |
dc.subject | allantoside | |
dc.subject | cerebroside | |
dc.subject | chaxine C | |
dc.subject | cytotoxic agent | |
dc.subject | ergosterol | |
dc.subject | ergosterol epoxide | |
dc.subject | fungal extract | |
dc.subject | methylcholesta 7,22 diene 3beta,5alpha,6beta triol | |
dc.subject | n [10 (13,14 methylenedioxyphenyl) )pentadienoyl]pyrrolidine | |
dc.subject | norincisterol A3 | |
dc.subject | piperazine derivative | |
dc.subject | unclassified drug | |
dc.subject | veratryl alcohol | |
dc.subject | antineoplastic agent | |
dc.subject | cerebroside | |
dc.subject | antineoplastic activity | |
dc.subject | Article | |
dc.subject | Ascomycetes | |
dc.subject | carbon nuclear magnetic resonance | |
dc.subject | drug cytotoxicity | |
dc.subject | drug isolation | |
dc.subject | drug structure | |
dc.subject | electrospray mass spectrometry | |
dc.subject | HCT 116 cell line | |
dc.subject | HeLa cell line | |
dc.subject | heteronuclear multiple bond correlation | |
dc.subject | HT-29 cell line | |
dc.subject | human | |
dc.subject | human cell | |
dc.subject | IC50 | |
dc.subject | infrared spectroscopy | |
dc.subject | MCF-7 cell line | |
dc.subject | MTT assay | |
dc.subject | proton nuclear magnetic resonance | |
dc.subject | stereochemistry | |
dc.subject | Vero cell line | |
dc.subject | Xylaria allantoidea | |
dc.subject | chemistry | |
dc.subject | fermentation | |
dc.subject | isolation and purification | |
dc.subject | metabolism | |
dc.subject | nuclear magnetic resonance spectroscopy | |
dc.subject | tumor cell line | |
dc.subject | Xylariales | |
dc.subject | Antineoplastic Agents | |
dc.subject | Cell Line, Tumor | |
dc.subject | Cerebrosides | |
dc.subject | Fermentation | |
dc.subject | Humans | |
dc.subject | Magnetic Resonance Spectroscopy | |
dc.subject | Xylariales | |
dc.title | A new cerebroside and the cytotoxic constituents isolated from Xylaria allantoidea SWUF76 | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Natural Product Research. Vol 31, No.12 (2017), p.1422-1430 | |
dc.identifier.doi | 10.1080/14786419.2016.1258559 | |
Appears in Collections: | Scopus 1983-2021 |
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