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DC Field | Value | Language |
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dc.contributor.author | Sawadsitang S. | - |
dc.contributor.author | Suwannasai N. | - |
dc.contributor.author | Mongkolthanaruk W. | - |
dc.contributor.author | Ahmadi P. | - |
dc.contributor.author | McCloskey S. | - |
dc.date.accessioned | 2021-04-05T03:05:27Z | - |
dc.date.available | 2021-04-05T03:05:27Z | - |
dc.date.issued | 2018 | - |
dc.identifier.issn | 14786419 | - |
dc.identifier.other | 2-s2.0-85034843617 | - |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/12737 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85034843617&doi=10.1080%2f14786419.2017.1405414&partnerID=40&md5=e3a6ba30be494464006feb31a754ffb7 | - |
dc.description.abstract | The secondary metabolites of Xylaria cf. cubensis SWUF08-86 fungus were investigated, and the chromatographic separation of the crude extracts yielded seventeen compounds. The structure elucidation by spectroscopic analysis including 1D and 2D NMR and the comparison of these data with literature, along with HREIMS spectrometry, revealed one new amino amidine derivative (1), together with five known simple cyclic dipeptide analogs, diketopiperazines (2–6) and eleven other known compounds, including one hemi-cycline (10), three aromatic derivatives (11–13), one sesquiterpene (14) and three sterols (15–17). The isolated compounds were screened for anticancer and anti-pathogenic bacterial and fungal activities. Based on this work, Xylaria cf. cubensis SWUF08-86 has proven to be a diverse secondary metabolites producer. © 2017, © 2017 Informa UK Limited, trading as Taylor & Francis Group. | - |
dc.subject | 1h indole | - |
dc.subject | 4 hydroxybenzoic acid | - |
dc.subject | amidine | - |
dc.subject | amino amidine derivative | - |
dc.subject | amphotericin B | - |
dc.subject | cycline | - |
dc.subject | dipeptide | - |
dc.subject | doxorubicin | - |
dc.subject | ergosterol | - |
dc.subject | ergosterol peroxide | - |
dc.subject | piperazinedione | - |
dc.subject | sesquiterpene | - |
dc.subject | stellasterol | - |
dc.subject | sterol | - |
dc.subject | tamoxifen | - |
dc.subject | unclassified drug | - |
dc.subject | vancomycin | - |
dc.subject | amidine | - |
dc.subject | antifungal agent | - |
dc.subject | antiinfective agent | - |
dc.subject | antineoplastic agent | - |
dc.subject | dipeptide | - |
dc.subject | Acinetobacter baumannii | - |
dc.subject | Alternaria brassicicola | - |
dc.subject | antibacterial activity | - |
dc.subject | antifungal activity | - |
dc.subject | antineoplastic activity | - |
dc.subject | Article | - |
dc.subject | chemical analysis | - |
dc.subject | chemical structure | - |
dc.subject | chromatography | - |
dc.subject | controlled study | - |
dc.subject | Curvularia lunata | - |
dc.subject | drug cytotoxicity | - |
dc.subject | drug structure | - |
dc.subject | Enterococcus faecium | - |
dc.subject | fungus | - |
dc.subject | minimum inhibitory concentration | - |
dc.subject | nonhuman | - |
dc.subject | nuclear magnetic resonance | - |
dc.subject | spectroscopy | - |
dc.subject | Thailand | - |
dc.subject | Xylaria cf. cubensis | - |
dc.subject | chemistry | - |
dc.subject | isolation and purification | - |
dc.subject | metabolism | - |
dc.subject | nuclear magnetic resonance spectroscopy | - |
dc.subject | Xylariales | - |
dc.subject | Amidines | - |
dc.subject | Anti-Bacterial Agents | - |
dc.subject | Antifungal Agents | - |
dc.subject | Antineoplastic Agents | - |
dc.subject | Dipeptides | - |
dc.subject | Magnetic Resonance Spectroscopy | - |
dc.subject | Molecular Structure | - |
dc.subject | Xylariales | - |
dc.title | A new amino amidine derivative from the wood-decaying fungus Xylaria cf. cubensis SWUF08-86 | - |
dc.type | Article | - |
dc.rights.holder | Scopus | - |
dc.identifier.bibliograpycitation | Natural Product Research. Vol 32, No.19 (2018), p.2260-2267 | - |
dc.identifier.doi | 10.1080/14786419.2017.1405414 | - |
Appears in Collections: | Scopus 1983-2021 |
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