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dc.contributor.authorJiradej Manosroien_US
dc.contributor.authorRujida Wilairaten_US
dc.contributor.authorAranya Manosroien_US
dc.date.accessioned2018-09-10T04:00:07Z-
dc.date.available2018-09-10T04:00:07Z-
dc.date.issued2007-03-01en_US
dc.identifier.issn17445116en_US
dc.identifier.issn13880209en_US
dc.identifier.other2-s2.0-34247554195en_US
dc.identifier.other10.1080/13880200701214862en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=34247554195&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/60827-
dc.description.abstractTwenty-two methanol and chloroform crude extracts from Guttiferae (Hypericum hookerianum Wight & Arn; Garcinia speciosa Wall; Garcinia xanthochymus Hook. F. ex T. Anderson; Cratoxylum formosum subsp. pruniflorum (Kurz) Gogel; and Calophyllum polyanthum Wall ex Choisy) and Schisandraceae families (Schisandra verruculosa Gagnap) collected from the northern region of Thailand were tested for antiproliferative activity on B16F10 (melanoma), HeLa (cervical carcinoma), and KB (epidermoid carcinoma) human cancer cell lines using the sulforhodamine-B (SRB) binding assay. All crude extracts showed an interesting antiproliferative activity with a dose-response relationship. The chloroform extract from leaves of G. speciosa was the most potent in inhibiting cancer cell growth with the GI50 of 4, 6.6, and 3.7 μg/mL in HeLa, KB, and B16F10 cell lines, which were 13-, 20- and 142-fold less potent than doxurubicin, respectively. The information from this study can explain the use of these plants in Thai traditional medicine and suggests the potential for further development of these extracts to new pharmaceuticals. © 2007 Informa Healthcare.en_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectHealth Professionsen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleAnti-proliferative activity of extracts from Thai plants in Guttiferae and Schisandraceae families on human cancer cell linesen_US
dc.typeJournalen_US
article.title.sourcetitlePharmaceutical Biologyen_US
article.volume45en_US
article.stream.affiliationsChiang Mai Universityen_US
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