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dc.contributor.authorR. Kampongen_US
dc.contributor.authorW. Pompimonen_US
dc.contributor.authorP. Meepowpanen_US
dc.contributor.authorS. Sukdeeen_US
dc.contributor.authorP. Sombutsirien_US
dc.contributor.authorN. Nantasaenen_US
dc.contributor.authorS. Krachodnoken_US
dc.date.accessioned2018-09-04T09:31:16Z-
dc.date.available2018-09-04T09:31:16Z-
dc.date.issued2013-11-19en_US
dc.identifier.issn0972768Xen_US
dc.identifier.other2-s2.0-84887557581en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84887557581&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/52733-
dc.description.abstract(-)-7-O-Acetylgoniodiol (1B) together with goniothalamin (2) and pinocembrin (3), have been isolated from leaves and twigs of Goniothalamus griffithii. All compounds were identified by spectroscopic analyses and comparison with published data. 1B can be formed by recrystallization from EtOH/acetone and its stereochemistry was further confirmed by X-ray crystallographic analysis. Goniothalamin exhibited most potent cytotoxicity against P-388, KB, Col-2, MCF-7, Lu-1, A549, T24, ASK, HEK-293 and cells with ED50values of 0.19, 0.56, 0.36, 0.56, 0.54, 0.67, 0.39, 0.67 and 0.50 μg/mL, respectively. In addition, 1B was also showed high selective inhibitory effect on the P-388, KB and HEK-293 with ED50values of 3.31, 3.26 and 1.89 μg/mL.en_US
dc.subjectMathematicsen_US
dc.title(-)-7-O-acetylgoniodiol as cancer chemopreventive agent from Goniothalamus Griffithiien_US
dc.typeJournalen_US
article.title.sourcetitleInternational Journal of Chemical Sciencesen_US
article.volume11en_US
article.stream.affiliationsRajabhat Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsThe Forest Herbarium, Thailand Ministry of Natural Resources and Environmenten_US
Appears in Collections:CMUL: Journal Articles

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