Pentacyclic triterpenes from branches of Maytenus robusta and in vitro cytotoxic property against 4T1 cancer cells

Two new friedelane-type compounds 1 and 2 and five known pentacyclic triterpenes were isolated from branches of Maytenus robusta. Their structures were identified as 3,16-dioxo-29-hydroxyfriedelane (1), 3-oxo-16b,29-dihydroxyfriedelane (2), 3-oxofriedelane (3), 3b-friedelinol (4), 3,16-dioxofriedelane (5), 3-oxo-29-hydroxyfriedelane (6), and 3,16-dioxo-12a-hydroxyfriedelane (7). The structures and the stereochemistry of triterpenes 1 and 2 were established through infrared (IR), 1D/2D nuclear magnetic resonance (NMR), high-resolution atmospheric pressure chemical ionization mass spectrometry (HR-APCIMS) spectral data and powder X-ray diffraction. The in vitro cytotoxic property of triterpenes 1 to 6 on 4T1 murine breast cancer cells was evaluated. The triterpenes 1 and 2 showed cytotoxic activity against 4T1 cells at a lower concentration.

Bibliographic Details

Main Authors:	Sousa,Grasiely Faria de, Soares,Daniel Crístian Ferreira, Mussel,Wagner da Nova, Pompeu,Nana Flora Elias, Silva,Grácia Divina de Fátima, Vieira Filho,Sidney Augusto, Duarte,Lucienir Pains
Format:	Digital revista
Language:	English
Published:	Sociedade Brasileira de Química 2014
Online Access:	http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532014000800004
Tags:	Add Tag No Tags, Be the first to tag this record!