Please use this identifier to cite or link to this item: https://repository.cihe.edu.hk/jspui/handle/cihe/2022
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dc.contributor.authorBligh, Annie Sim Wanen_US
dc.contributor.otherWu, T.-
dc.contributor.otherCheng, X.-M.-
dc.contributor.otherChou, G.-X.-
dc.contributor.otherWang, Z.-T.-
dc.contributor.otherBashall, A.-
dc.contributor.otherBranford-White, C.-
dc.date.accessioned2021-12-09T06:48:33Z-
dc.date.available2021-12-09T06:48:33Z-
dc.date.issued2005-
dc.identifier.urihttps://repository.cihe.edu.hk/jspui/handle/cihe/2022-
dc.description.abstractTwo new multiflorane triterpene esters, (3α,7β)-3,7,29-trihydroxymultiflor-8-ene-3,29-diyl dibenzoate (<b>2</b>) and (3α)-3,29-dihydroxy-7-oxomultiflor-8-ene-3,29-diyl dibenzoate (<b>3</b>) have been isolated from the CHCl<sub>3</sub> extract of the seeds of <i>Trichosanthes kirilowii</i>, together with two known compounds, (3α,5α,22E)-24-ethylcholesta-7,22,25(27)-trien-3-ol and darutigenol. The structures of the new compounds were elucidated on the basis of extensive NMR experiments, and by means of an X-ray crystallographic analysis of <b>2</b>. A preliminary cytotoxicity assay showed that <b>2</b> and <b>3</b> are basically inactive against the K562 cell line.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.relation.ispartofHelvetica Chimica Actaen_US
dc.titleMultiflorane triterpene esters from the seeds of Trichosanthes kirilowiien_US
dc.typejournal articleen_US
dc.identifier.doi10.1002/hlca.200590202-
dc.contributor.affiliationSchool of Health Sciencesen_US
dc.relation.issn1522-2675en_US
dc.description.volume88en_US
dc.description.issue10en_US
dc.description.startpage2617en_US
dc.description.endpage2623en_US
dc.cihe.affiliatedNo-
item.fulltextWith Fulltext-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.cerifentitytypePublications-
item.openairetypejournal article-
item.languageiso639-1en-
crisitem.author.deptS.K. Yee School of Health Sciences-
crisitem.author.orcid0000-0002-4757-2159-
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