Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/51375
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dc.contributor.authorSaranyoo Klaiklayen_US
dc.contributor.authorVatcharin Rukachaisirikulen_US
dc.contributor.authorYaowapa Sukpondmaen_US
dc.contributor.authorSouwalak Phongpaichiten_US
dc.contributor.authorJirayu Buatongen_US
dc.contributor.authorBoonsom Bussabanen_US
dc.date.accessioned2018-09-04T06:01:00Z-
dc.date.available2018-09-04T06:01:00Z-
dc.date.issued2012-07-01en_US
dc.identifier.issn19763786en_US
dc.identifier.issn02536269en_US
dc.identifier.other2-s2.0-84864951083en_US
dc.identifier.other10.1007/s12272-012-0701-yen_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84864951083&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/51375-
dc.description.abstractTwo new succinic acid derivatives, xylacinic acids A (1) and B (2), along with seven known compounds, including one succinic acid derivative (3), three mellein derivatives (4-6), cytochalasin D (7), 2-chloro-5-methoxy-3- methylcyclohexa-2,5-diene-1,4-dione (8) and isosclerone (9), were isolated from the mangrove-derived fungus Xylaria cubensis PSU-MA34. Their structures were established by spectroscopic evidence. They were evaluated for cytotoxicity against KB cells and antibacterial activity against Staphylococcus aureus ATCC 25923 and methicillin- resistant S. aureus.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleMetabolites from the mangrove-derived fungus xylaria cubensis PSU-MA34en_US
dc.typeJournalen_US
article.title.sourcetitleArchives of Pharmacal Researchen_US
article.volume35en_US
article.stream.affiliationsPrince of Songkla Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
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