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dc.contributor.authorIttipon Siridechakornen_US
dc.contributor.authorSarot Cheenprachaen_US
dc.contributor.authorThunwadee Ritthiwigromen_US
dc.contributor.authorWong Phakhodeeen_US
dc.contributor.authorSuwanna Deachathaien_US
dc.contributor.authorTheeraphan Machanen_US
dc.contributor.authorNirun Ruankeawen_US
dc.contributor.authorSurat Laphookhieoen_US
dc.date.accessioned2018-09-04T09:43:35Z-
dc.date.available2018-09-04T09:43:35Z-
dc.date.issued2014-02-01en_US
dc.identifier.issn18767486en_US
dc.identifier.issn18743900en_US
dc.identifier.other2-s2.0-84891603038en_US
dc.identifier.other10.1016/j.phytol.2013.12.003en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84891603038&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/53090-
dc.description.abstractThe first phytochemical investigation of Caesalpinia furfuracea twigs led to the isolation and identification of four new compounds including two isopimarane diterpenes, caesalfurfuric acids A (1) and B (2), and two flavans, (2R)-caesalflavans A (5) and B (6), together with four known compounds, 4-epi-isopimaric acid (3), methyl (E)-3-(3,4-dihydroxyphenyl)acrylate (4), (E)-resveratrol (7) and oxyresveratrol (8). Their structures were elucidated by intensive spectroscopic analysis. Compound 1 was found to exhibit antibacterial activity against MRSA SK1 with an MIC value of 16 μg/mL. © 2013 Phytochemical Society of Europe. Published by Elsevier B.V. All rights reserved.en_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleIsopimarane diterpenes and flavan derivatives from the twigs of Caesalpinia furfuraceaen_US
dc.typeJournalen_US
article.title.sourcetitlePhytochemistry Lettersen_US
article.volume7en_US
article.stream.affiliationsMae Fah Luang Universityen_US
article.stream.affiliationsUniversity of Phayaoen_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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