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dc.contributor.authorMasahiko Isakaen_US
dc.contributor.authorPanida Chinthanomen_US
dc.contributor.authorPranee Rachtaweeen_US
dc.contributor.authorKitlada Srichomthongen_US
dc.contributor.authorPrasert Srikitikulchaien_US
dc.contributor.authorPalangpon Kongsaereeen_US
dc.contributor.authorSamran Prabpaien_US
dc.contributor.otherThailand National Center for Genetic Engineering and Biotechnologyen_US
dc.contributor.otherFaculty of Scienceen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-11-23T10:44:29Z-
dc.date.available2018-11-23T10:44:29Z-
dc.date.issued2015-05-28en_US
dc.identifier.citationJournal of Antibiotics. Vol.68, No.5 (2015), 334-338en_US
dc.identifier.issn18811469en_US
dc.identifier.issn00218820en_US
dc.identifier.other2-s2.0-84930193261en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84930193261&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/36431-
dc.description.abstract© 2015 Japan Antibiotics Research Association All rights reserved. Two new hydroanthraquinones, paradictyoarthrins A (1) and B (2), were isolated from the mangrove-derived fungus Paradictyoarthrinium diffractum BCC 8704. Structures of the new compounds were elucidated by analyses of the NMR spectroscopic and mass spectrometry data. The absolute configuration of 1 was determined by X-ray crystallography. These compounds exhibited cytotoxic activities.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84930193261&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleCytotoxic hydroanthraquinones from the mangrove-derived fungus Paradictyoarthrinium diffractum BCC 8704en_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1038/ja.2014.153en_US
Appears in Collections:Scopus 2011-2015

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