Synthesis and cytotoxicity evaluation of A-ring derivatives of cycloartanone

Publication date: September 2017 Source:Phytochemistry Letters, Volume 21 Author(s): E. Elisabeth Zambrano, Adriana G. Casas, Gabriela M. Di Venosa, María L. Uriburu, Fernando J. Duran, Jorge A. Palermo Sixteen derivatives, eight of which are new compounds, were prepared from cycloartenone (1) and cycloartanone (2), and the cytotoxic activity of 14 of these compounds, together with 1 and 2, was evaluated against a panel of four cell lines. Compound 1 was obtained from the epiphyte plant Tillandsia tenuifolia collected at Salta, Argentina. Due to chemoselectivity and regioselectivity problems observed in the reactions of compound 1, this substance was hydrogenated to compound 2. The attempted transformations were focused on ring A of the cited triterpenes with the aim to verify previous structure-activity relationships obtained from related compounds. The cytotoxicity results of the derivatives showed that only the diosphenol 13 displayed significant activity against all the tested cell lines. These results show that an oxidized side chain, for example an ether bridge between the side chain and ring D, is necessary for the cytotoxic activity of cycloartane derivatives. Graphical abstract
Source: Phytochemistry Letters - Category: Chemistry Source Type: research