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dc.contributor.author Könye Rita
dc.contributor.author Tóth Gergő
dc.contributor.author Sólyomváry Anna
dc.contributor.author Mervai Zsolt
dc.contributor.author Zürn M
dc.contributor.author Baghy Kornélia
dc.contributor.author Kovalszky Ilona
dc.contributor.author Horváth Péter
dc.contributor.author Perlné Molnár Ibolya
dc.contributor.author Noszál Béla
dc.contributor.author Béni Szabolcs
dc.contributor.author Boldizsár Imre
dc.date.accessioned 2018-06-22T10:31:08Z
dc.date.available 2018-06-22T10:31:08Z
dc.date.issued 2018
dc.identifier 85045559589
dc.identifier.citation pagination=413-419; journalVolume=127; journalTitle=FITOTERAPIA;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/5491
dc.identifier.uri doi:10.1016/j.fitote.2018.04.007
dc.description.abstract While analyzing the fruit composition of nine European Cirsium species representing three sections (i.e., Cephalonoplos, Chamaeleon and Eriolepis), four lignans, three neolignans and three sesquineolignans were determined and used as chemotaxonomic markers. Among them, desmethyl balanophonin and desmethyl picrasmalignan were determined for the first time in the plant kingdom, as the main metabolites of the Chamaeleon section. Prebalanophonin and prepicrasmalignan, identified so far exclusively in C. eriophorum, were also confirmed in C. boujartii and C. vulgare, highlighting the chemotaxonomic significance of these compounds in the Eriolepis section. The antiproliferative assay of the compounds isolated from their optimum sources, confirmed a dose-dependent inhibitory effect of the structures bearing the 4′,7-epoxy moiety (balanophonin, picrasmalignan, desmethyl balanophonin, desmethyl picrasmalignan) against SW480 colon cancer cells, while those bearing the 4′,7-dihydroxy motif (prebalanophonin, prepicrasmalignan) were inactive. © 2018 Elsevier B.V.
dc.relation.ispartof urn:issn:0367-326X
dc.title Chemodiversity of Cirsium fruits: Antiproliferative lignans, neolignans and sesquineolignans as chemotaxonomic markers
dc.type Journal Article
dc.date.updated 2018-05-29T12:13:08Z
dc.language.rfc3066 en
dc.identifier.mtmt 3368249
dc.contributor.department SE/GYTK/Farmakognózia Intézet
dc.contributor.department SE/GYTK/Gyógyszerészi Kémiai Intézet
dc.contributor.department SE/AOK/I/I. Sz. Patológiai és Kísérleti Rákkutató Intézet
dc.contributor.institution Semmelweis Egyetem
dc.mtmt.swordnote FELTÖLTŐ: Reményi Zsuzsa - titkarsag@drog.sote.hu N1 Article in Press


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