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DC Field | Value | Language |
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dc.contributor.author | Patjana T. | |
dc.contributor.author | Jantaharn P. | |
dc.contributor.author | Katrun P. | |
dc.contributor.author | Mongkolthanaruk W. | |
dc.contributor.author | Suwannasai N. | |
dc.contributor.author | Senawong T. | |
dc.contributor.author | Tontapha S. | |
dc.contributor.author | Amornkitbumrung V. | |
dc.contributor.author | McCloskey S. | |
dc.date.accessioned | 2022-03-10T13:17:26Z | - |
dc.date.available | 2022-03-10T13:17:26Z | - |
dc.date.issued | 2021 | |
dc.identifier.issn | 14786419 | |
dc.identifier.other | 2-s2.0-85071024282 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/17539 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85071024282&doi=10.1080%2f14786419.2019.1652292&partnerID=40&md5=38a2f447c8d906b70394b5545a002d26 | |
dc.description.abstract | The ongoing search for anti-cancer agents from microorganisms led to the isolation of four new compounds including 6-ethyl-8-hydroxy-4H-chromen-4-one (1), 6-ethyl-7,8-dihydroxy-4H-chromen-4-one (2), (3S)-3,4-dihydro-8-hydroxy-7-methoxy-3-methylisocoumarin (3) and (3S)-3,4-dihydro-5,7,8-trihydroxy-3-methylisocoumarin (4), together with eleven known compounds (5–15) from Xylaria sp. SWUF09-62 fungus. The chemical structures were deduced from IR, 1D and 2D NMR, and MS data. The absolute configurations of 3 and 4 were determined by ECD experiment. Compounds 2 and 4 indicated possible chemo-prevention and chemo-therapeutic properties, exhibited anti-inflammatory properties by reducing nitric oxide production in LPS-stimulated RAW264.7 cells (IC50 = 1.57 ± 0.25 and 3.02 ± 0.27 μg/mL) and cytotoxicity against HT29 cells (IC50 = 16.46 ± 0.48 and 97.78 ± 7.14 μg/mL). © 2019 Informa UK Limited, trading as Taylor & Francis Group. | |
dc.subject | 3,4 dihydro 5,7,8 trihydroxy 3 methylisocoumarin | |
dc.subject | 3,4 dihydro 8 hydroxy 7 methoxy 3 methylisocoumarin | |
dc.subject | 6 ethyl 7,8 dihydroxy 4h chromen 4 one | |
dc.subject | 6 ethyl 8 hydroxy 4h chromen 4 one | |
dc.subject | antiinflammatory agent | |
dc.subject | cytotoxic agent | |
dc.subject | diclofenac | |
dc.subject | nitric oxide | |
dc.subject | unclassified drug | |
dc.subject | antiinflammatory agent | |
dc.subject | antineoplastic agent | |
dc.subject | biological product | |
dc.subject | lipopolysaccharide | |
dc.subject | antiinflammatory activity | |
dc.subject | Article | |
dc.subject | cancer cell | |
dc.subject | carbon nuclear magnetic resonance | |
dc.subject | cell viability | |
dc.subject | chemical structure | |
dc.subject | chemoprophylaxis | |
dc.subject | controlled study | |
dc.subject | cytotoxicity | |
dc.subject | fungus | |
dc.subject | IC50 | |
dc.subject | infrared spectroscopy | |
dc.subject | macrophage | |
dc.subject | mass spectrometry | |
dc.subject | MTT assay | |
dc.subject | nonhuman | |
dc.subject | nuclear magnetic resonance | |
dc.subject | Xylariales | |
dc.subject | animal | |
dc.subject | chemistry | |
dc.subject | HCT 116 cell line | |
dc.subject | HT-29 cell line | |
dc.subject | human | |
dc.subject | metabolism | |
dc.subject | mouse | |
dc.subject | nuclear magnetic resonance spectroscopy | |
dc.subject | preclinical study | |
dc.subject | RAW 264.7 cell line | |
dc.subject | Animals | |
dc.subject | Anti-Inflammatory Agents | |
dc.subject | Antineoplastic Agents | |
dc.subject | Biological Products | |
dc.subject | Drug Evaluation, Preclinical | |
dc.subject | HCT116 Cells | |
dc.subject | HT29 Cells | |
dc.subject | Humans | |
dc.subject | Lipopolysaccharides | |
dc.subject | Magnetic Resonance Spectroscopy | |
dc.subject | Mice | |
dc.subject | Molecular Structure | |
dc.subject | Nitric Oxide | |
dc.subject | RAW 264.7 Cells | |
dc.subject | Xylariales | |
dc.title | Anti-inflammatory and cytotoxic agents from Xylaria sp. SWUF09-62 fungus | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Natural Product Research. Vol 35, No.12 (2021), p.2010-2019 | |
dc.identifier.doi | 10.1080/14786419.2019.1652292 | |
Appears in Collections: | Scopus 1983-2021 |
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