Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/67569
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dc.contributor.authorThanika Promchaien_US
dc.contributor.authorThanaphat Thaimaen_US
dc.contributor.authorRoonglawan Rattanajaken_US
dc.contributor.authorSumalee Kamchonwongpaisanen_US
dc.contributor.authorStephen G. Pyneen_US
dc.contributor.authorThunwadee Limtharakulen_US
dc.date.accessioned2020-04-02T14:55:48Z-
dc.date.available2020-04-02T14:55:48Z-
dc.date.issued2019-01-01en_US
dc.identifier.issn14786427en_US
dc.identifier.issn14786419en_US
dc.identifier.other2-s2.0-85076485476en_US
dc.identifier.other10.1080/14786419.2019.1679139en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85076485476&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/67569-
dc.description.abstract© 2019, © 2019 Informa UK Limited, trading as Taylor & Francis Group. A new farnesylindole, (R)-3-(8'-hydroxyfarnesyl)-indole (1), as a scalemic mixture (33% ee) along with nine known compounds (2-10), including one farnesylindole, three flavanones, three flavone derivatives and two chalcone derivatives were isolated from the methanolic crude extract of the flowers from Anomianthus dulcis. All compounds were purified by appropriate chromatographic techniques and their structures elucidated by spectroscopic methods. Compounds 1, 2 and 8 showed moderate antiplasmodial activities against TM4/8.Two and K1CB1 strains of which compound 2 displayed the best activity with IC50 values of 27.9 ± 2.57 and 21.4 ± 1.68 µM, respectively. In addition, compound 1 also presented modest cytotoxicity against a KB cell line with an IC50 value of 22.3 ± 0.39 µM. None of these compounds showed cytotoxicity against Vero cells.en_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.title(R)-3-(8'-Hydroxyfarnesyl)-indole and other chemical constituents from the flowers of Anomianthus dulcis and their antimalarial and cytotoxic activitiesen_US
dc.typeJournalen_US
article.title.sourcetitleNatural Product Researchen_US
article.stream.affiliationsUniversity of Wollongongen_US
article.stream.affiliationsThailand National Science and Technology Development Agencyen_US
article.stream.affiliationsChiang Mai Universityen_US
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