Publication:
Cytotoxic sesquiterpenoids and diarylheptanoids from the rhizomes of Curcuma elata Roxb.

dc.contributor.authorRatchanaporn Chokchaisirien_US
dc.contributor.authorPrapapan Pimkaewen_US
dc.contributor.authorPawinee Piyachaturawaten_US
dc.contributor.authorRattana Chalermglinen_US
dc.contributor.authorApichart Suksamrarnen_US
dc.contributor.otherRamkhamhaeng Universityen_US
dc.contributor.otherUniversity of Phayaoen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherChandrakasem Rajabhat Universityen_US
dc.date.accessioned2018-11-09T01:47:58Z
dc.date.available2018-11-09T01:47:58Z
dc.date.issued2014-01-01en_US
dc.description.abstractThe present study was aimed to investigate the chemical constituents of Curcuma elata Roxb. (Zingiberaceae) rhizomes originating in Thailand. Ten sesquiterpenes, germacrone (1), curzerenone (2), isofuranodienone (3), furanodienone (4), curdione (5), neocurdione (6), zederone (7), curcumenone (8), 13-hydroxygermacrone (9) and zedoarondiol (10), and four diarylheptanoids, 3-hydroxy-5-platyphyllone (11), (3S)-1,7-bis(4-hydroxyphenyl)-(6E)-6-hepten-3-ol (12), centrolobol (13) and (3S)-1-(3,4-dihydroxyphenyl)-7-(4-hydroxyphenyl)-(6E)-6-hepten-3-ol (14) were isolated for the first time from the rhizomes of this plant. The structures of the isolated compounds were identified by comparison of the spectroscopic and physical data with those of the reported values and the stereochemistry at the asymmetric carbon was determined by the modified Mosher's method and, in some cases, was confirmed by comparison of optical rotation data with literature. Compounds 12 and 13 exhibited strong cytotoxic activity against KB cell line, whereas compounds 4, 9 and 12-14 showed strong cytoxicity against NCI-H187 cell line. © 2014 ACG Publications. All rights reserved.en_US
dc.identifier.citationRecords of Natural Products. Vol.8, No.1 (2014), 46-50en_US
dc.identifier.issn13076167en_US
dc.identifier.other2-s2.0-84887831844en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/33146
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84887831844&origin=inwarden_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleCytotoxic sesquiterpenoids and diarylheptanoids from the rhizomes of Curcuma elata Roxb.en_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84887831844&origin=inwarden_US

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