Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/49744
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dc.contributor.authorThanapat Sastrarujien_US
dc.contributor.authorSukanda Chaiyongen_US
dc.contributor.authorAraya Jatisatienren_US
dc.contributor.authorStephen G. Pyneen_US
dc.contributor.authorAlison T. Ungen_US
dc.contributor.authorWilford Lieen_US
dc.date.accessioned2018-09-04T04:17:31Z-
dc.date.available2018-09-04T04:17:31Z-
dc.date.issued2011-01-28en_US
dc.identifier.issn15206025en_US
dc.identifier.issn01633864en_US
dc.identifier.other2-s2.0-79951545662en_US
dc.identifier.other10.1021/np100668sen_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79951545662&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/49744-
dc.description.abstractA new stemofoline alkaloid, (2'S)-hydroxy-(11S,12R)-dihydrostemofoline (3), new stemofurans M-R (8-13), and known compounds stemofoline (1), (2'S)-hydroxystemofoline (2), stemofuran E (4), stemofuran F (5), stemofuran J (6), and stilbostemin F (7) have been isolated from the root extracts of Stemona aphylla. The structures and relative configurations of these new compounds have been determined by spectroscopic data interpretation and from semisynthetic studies. These natural and semisynthetic alkaloids were tested for acetylcholinesterase inhibitory activities and were found to be 10-20 times less active than 1',2'-didehydrostemofoline itself. Stemofurans 4, 6, 8, 11, and 13 were tested for their antibacterial and antifungal activities. Three of these showed antibacterial activities against MRSA with MIC values of 15.6 μg/mL. © 2011 American Chemical Society and American Society of Pharmacognosy.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectMedicineen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titlePhytochemical studies on Stemona aphylla: Isolation of a new stemofoline alkaloid and six new stemofuransen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Natural Productsen_US
article.volume74en_US
article.stream.affiliationsUniversity of Wollongongen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsUniversity of Technology Sydneyen_US
Appears in Collections:CMUL: Journal Articles

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