Synthesis and cytotoxicity evaluation of A-ring derivatives of cycloartanone

ZAMBRANO E ; CASAS A; DI VENOSA G; URIBURU M; DURAN F; PALERMO J

PHYTOCHEMISTRY LETTERS

ELSEVIER SCIENCE BV

Lugar: Amsterdam; Año: 2017 vol. 21 p. 200 - 205

1874-3900

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 enuifolia 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 cited0 triterpenes with the aim to verify previous structure-activity relationships obtained from elated compounds.The cytotoxicity results of the derivatives showed that only the diosphenol 13 displayed significant activityagainst all the tested cell lines. These results show that an oxidized side hain, for example an ether bridge between the side chain and ring D, is necessary for the cytotoxic activity of cycloartane derivatives.