Major terpenoids from flowers and their cytotoxic activity .

Nat Prod Res

c Faculty of Biotechnology, Department of Cell Biology , Jagiellonian University, Kraków , Poland.

Published: June 2019

In addition to known constituents of , an acetone extract from ray florets of the plant yielded: 5,5'-dibutoxy-2,2'-bifuran (), 5,5'-diisobutoxy-2,2'-bifuran (), α-tocopherol (), β-tocopherol (), loliolide palmitate (), a mixture of calenduladiol esters - 16β-hydroxylupeol-3-O-palmitate () and 16β-hydroxylupeol-3-O-myristate (), 1-epiinuviscolide (), inuviscolide (), 3-epiisotelekin (), 4α-hydroxy-9β,10β-epoxy-1β(H)-11(13)-guaien-8α,12-olide (), 4α-hydroxy-1β(H)-9(10),11(13)-guaiadien-8α,12-olide (), loliolide () and 4β,10β-dihydroxy-1α(H),5α(H)-11(13)-guaien-8α,12-olide (). Calenduladiol esters and asperilin () were the major constituents of the extract. Their cytotoxic effect on human normal prostate epithelial cells (PNT-2), human prostate carcinoma cell lines, human skin fibroblasts (HSF) and human melanoma cell lines was examined . Triterpene esters showed no cytotoxicity against nearly all cell lines tested, except for Du145 prostate carcinoma cells (IC - 62.0 μΜ). Asperilin displayed activity against the cell lines under study, especially against three tested lines of melanomas (A375, IC - 17.6 μΜ, WM793, IC - 28.2 μΜ and Hs 294T, IC - 29.5 μΜ).

Download full-text PDF

Source
http://dx.doi.org/10.1080/14786419.2018.1437431DOI Listing

Publication Analysis

Top Keywords

cell lines
16
calenduladiol esters
8
prostate carcinoma
8
lines
5
major terpenoids
4
terpenoids flowers
4
flowers cytotoxic
4
cytotoxic activity
4
activity addition
4
addition constituents
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!