Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/50409
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dc.contributor.authorKanchana Pumsaliden_US
dc.contributor.authorHaruthai Thaisuchaten_US
dc.contributor.authorChatchanok Loetchutinaten_US
dc.contributor.authorNarong Nuntasaenen_US
dc.contributor.authorPuttinan Meepowpanen_US
dc.contributor.authorWilart Pompimonen_US
dc.date.accessioned2018-09-04T04:40:47Z-
dc.date.available2018-09-04T04:40:47Z-
dc.date.issued2010-12-01en_US
dc.identifier.issn15559475en_US
dc.identifier.issn1934578Xen_US
dc.identifier.other2-s2.0-78751539201en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=78751539201&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/50409-
dc.description.abstractChromatographic separation of the ethyl acetate extract of roots of Polyalthia cerasoides has led to the isolation of the new compound, 6,8-dihydroxy-7-methoxy-1-methyl-azafluorenone. This compound exhibited potent cytotoxic activities with IC50values in the range of 2.64-3.58 μg.mL-1for A549, GLC4 and GLC4/Adr cells, but was not recognized by ABCC1/MRP1 protein. The compound also showed very strong inhibition of M. tuberculosis using a broth microdilution method, with an MIC value of 0.78 μg.mL-1, which was equal to that of ofloxacin, one of the four antibiotic drugs used as a positive control.en_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectMedicineen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleA new azafluorenone from the roots of Polyalthia cerasoides and its biological activityen_US
dc.typeJournalen_US
article.title.sourcetitleNatural Product Communicationsen_US
article.volume5en_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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