Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/12136
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dc.contributor.authorPimjuk P.
dc.contributor.authorMongkolthanaruk W.
dc.contributor.authorSuwannasai N.
dc.contributor.authorSenawong T.
dc.contributor.authorTontapha S.
dc.contributor.authorAmornkitbumrung V.
dc.contributor.authorMcCloskey S.
dc.date.accessioned2021-04-05T03:02:00Z-
dc.date.available2021-04-05T03:02:00Z-
dc.date.issued2020
dc.identifier.issn10286020
dc.identifier.other2-s2.0-85097763387
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/12136-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85097763387&doi=10.1080%2f10286020.2020.1856095&partnerID=40&md5=b7085024b51acef721531ad7c610ee2e
dc.description.abstractA new α-pyrone derivative, namely annulopyronoate (1), together with the known isobenzofuranone, diphenyl ether, sesquiterpene, phenolic and diketopiperazine derivatives (2–12) were isolated from a filamentous fungus Annulohypoxylon stygium SWUF09-030. The structures were determined by analysis of spectroscopic and MS data. The absolute configuration of 1 was determined by comparison of experimental and calculated Electronic Circular Dichroism (ECD) spectra. Compounds 3–5 and 7 exhibited both anti-proliferative effects against HeLa, HT29, HCT116, MCF-7 and Vero cell lines and inhibition of nitric oxide (NO) production in lipopolysaccharide (LPS)-stimulated RAW264.7 macrophage cells. © 2020 Informa UK Limited, trading as Taylor & Francis Group.
dc.titleA new α-pyrone derivative from Annulohypoxylon stygium SWUF09-030
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationJournal of Asian Natural Products Research. (2020)
dc.identifier.doi10.1080/10286020.2020.1856095
Appears in Collections:Scopus 1983-2021

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