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Please use this identifier to cite or link to this item: http://uyr.uy.edu.mm/handle/123456789/121
dc.contributor.authorNwet Nwet Win
dc.contributor.authorIto, Takuya
dc.contributor.authorAimaiti, Simayijiang
dc.contributor.authorImagawa, Hiroshi
dc.contributor.authorHla Ngwe
dc.contributor.authorAbe, Ikuro
dc.contributor.authorMorita, Hiroyuki
dc.date.accessioned2016-11-07T18:53:51Z
dc.date.available2016-11-07T18:53:51Z
dc.date.issued2015
dc.identifierDOI: 10.1021/acs.jnatprod.5b00108
dc.identifier.urihttp://uyr.uy.edu.mm/handle/123456789/121
dc.descriptionJ. Nat. Prod., 2015, 78 (5), pp 1113–1118
dc.description.abstractEight new diterpenoids, kaempulchraols A–H (1–8), along with five known analogues were isolated from the CHCl3-soluble extract of rhizomes of Kaempferia pulchra of Myanmar. The structures of these compounds were elucidated using extensive spectroscopic techniques including X-ray diffraction analysis. All the isolates were tested for their antiproliferative activity against a panel of five human cancer cell lines (A549, human lung cancer; HeLa, human cervix cancer; PANC-1 and PSN-1, human pancreatic cancer; MDA-MB-231, human breast cancer) and TIG-3, normal human primary fibroblast cells. Kaempulchraol F (6) exhibited weak activity against the human pancreatic PSN-1 cell line with an IC50 value of 12.3 μM.
dc.titleKaempulchraols A−H, Diterpenoids from the Rhizomes of Kaempferia pulchra Collected in Myanmarlanguage
dc.typearticle


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