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dc.contributor.authorSirichan Tachaien_US
dc.contributor.authorNuchnipa Nuntawongen_US
dc.date.accessioned2018-09-05T02:51:26Z-
dc.date.available2018-09-05T02:51:26Z-
dc.date.issued2016-01-01en_US
dc.identifier.issn14786427en_US
dc.identifier.issn14786419en_US
dc.identifier.other2-s2.0-84959038291en_US
dc.identifier.other10.1080/14786419.2016.1146884en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84959038291&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/55063-
dc.description.abstract© 2016 Informa UK Limited, trading as Taylor & Francis Group. From the rhizomes of Etlingera pavieana (Pierre ex Gagnep.) R.M. Sm., four phenylpropens, (E)-3-(4-methoxyphenyl)prop-2-en-1-amine (1), (E)-4-methoxycinamaldehyde (2), (E)-4-methoxycinamic acid (3) and (E)-1-methoxy-4-(3-methoxyprop-1-enyl)benzene (4), together with two other compounds, (E)-((E)-3-(4-methoxyphenyl)allyl)3-(4-hydroxyphenyl)acrylate (5) and 4-methoxybenzoic acid (6) were isolated. This is the first report on the presence of all compounds in Etlingera. Compounds 1 and 5 have been previously synthesised, but this is the first report of their isolation from a natural source. Compound 5 exhibited weak activity against Mycobacterium tuberculosis with MIC 50.00 μg/mL and cytotoxic activity against the KB, MCF7 and NCI-H187 cells with IC50values of 25.11, 20.16 and 34.83 μg/mL, respectively.en_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.titleUncommon secondary metabolites from Etlingera pavieana rhizomesen_US
dc.typeJournalen_US
article.title.sourcetitleNatural Product Researchen_US
article.volume30en_US
article.stream.affiliationsChiang Mai Universityen_US
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