Oral Presentations: Pharmaceutical
Könye, Rita
Department of Pharmacognosy, Semmelweis University, Üllői út 26, Budapest 1085, Hungary
+36309576163
rita.konye@gmail.com
Taxon-specific accumulation of new, antiproliferative neo- and sesquineolignans in the fruits of Cirsium species
Rita Könye1,2
1 Department of Pharmacognosy, Semmelweis University, Budapest, Hungary
2 Department of Plant Anatomy, Institute of Biology, Eötvös Loránd University, Budapest, Hungary
Oral Presentations: Pharmaceutical
Doctoral School: Doctoral School of Pharmaceutical Sciences
Program: Modern Trends in Pharmaceutical Scientific Research
Supervisors: Szabolcs Béni, Imre Boldizsár
E-mail address: rita.konye@gmail.com
Neolignans (NeLis) and sesquineolignans (SeNeLis) are plant secondary metabolites possessing cytotoxic effects against cancer cells. Our recent results confirmed the presence of these compounds in the fruits of selected Cirsium species in high amount.
The goal of this study was to extend our previous research on the lignans through the analysis of various Cirsium fruits which has not been investigated in this respect before. The results revealed (i) the presence of two new natural compounds belonging to NeLi and to SeNeLi groups and (ii) the taxon-specific accumulation of these metabolites. Thus, according to the analysis of nine Cirsium species’ fruits, samples with optimum composition for high-yield isolation of pure compounds, were selected. Namely, from the fruits of C. rivulare the new NeLi and SeNeLi compounds were obtained (characteristics to the Chamaeleon section of Cirsium genus). While the fruits of C. eriophorum was used for the isolation of the already known NeLis (balanophonin and prebalanophonin) and SeNeLis (picrasmalignan and prepicrasmalignan). These compounds were found to be characteristic for the Eriolepis section.
All the isolated compounds were tested for their antiproliferative activity (APA) against the SW480 colon adenocarcinoma cell line, confirming the (i) APA of the new NeLi and SeNeLi compounds with equal IC50 value of 40 µM and (ii) structure-antiproliferative activity relationship of these natural compounds. In fact, our results demonstrate that the new NeLi and SeNeLi possess comparable APA as their structurally related methylated derivatives (NeLi balanophonin and SeNeLi picrasmalignan); however, the corresponding open-chain structures (prebalanophonin and prepicrasmalignan) are significantly less effective with IC50 over 100 µM.
Szabad
nem rendelkezett róla
1291
Rita Könye1,2
1 Department of Pharmacognosy, Semmelweis University, Budapest, Hungary
2 Department of Plant Anatomy, Institute of Biology, Eötvös Loránd University, Budapest, Hungary