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Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/52253
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dc.contributor.authorSarot Cheenprachaen_US
dc.contributor.authorThunwadee Ritthiwigromen_US
dc.contributor.authorSurat Laphookhieoen_US
dc.date.accessioned2018-09-04T09:22:43Z-
dc.date.available2018-09-04T09:22:43Z-
dc.date.issued2013-04-26en_US
dc.identifier.issn15206025en_US
dc.identifier.issn01633864en_US
dc.identifier.other2-s2.0-84876930059en_US
dc.identifier.other10.1021/np3006937en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84876930059&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/52253-
dc.description.abstractChemical investigation of an alkaloidal extract of Alstonia macrophylla bark led to the isolation and identification of two new nitrogenous derivatives, alstoniaphyllines A (1) and B (2), a new indole alkaloid, alstoniaphylline C (4), and eight known alkaloids (3, 5-11). Alstonisine (9) exhibited antiplasmodial activity against Plasmodium falciparum, with an IC50 of 7.6 μM. © 2013 The 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.titleAlstoniaphyllines A-C, unusual nitrogenous derivatives from the bark of Alstonia macrophyllaen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Natural Productsen_US
article.volume76en_US
article.stream.affiliationsUniversity of Phayaoen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsMae Fah Luang Universityen_US
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