Lupeol and its esters : NMR, powder XRD data and in vitro evaluation of cancer cell growth.

The triterpene lupeol (1) and some of its esters are secondary metabolites produced by species of Celastraceae family, which have being associated with cytotoxic activity. We report herein the isolation of 1, the semi-synthesis of eight lupeol esters and the evaluation of their in vitro activity aga...

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Bibliographic Details
Authors: Silva, Aline Teixeira Maciel, Magalhães, Cássia Gonçalves, Duarte, Lucienir Pains, Mussel, Wagner da Nova, Ruiz, Ana Lucia Tasca Gois, Shiozawa, Larissa, Carvalho, João Ernesto de, Trindade, Izabel Cristina, Vieira Filho, Sidney Augusto
Format: article
Status:Published version
Publication Date:2018
Country:Brasil
Institution:Universidade Federal de Ouro Preto (UFOP)
Repository:Repositório Institucional da UFOP
Language:English
OAI Identifier:oai:repositorio.ufop.br:123456789/9933
Online Access:http://www.repositorio.ufop.br/handle/123456789/9933
Access Level:Open access
Keyword:Lupeol/in vitro evaluation
Antiproliferative effect
Description
Summary:The triterpene lupeol (1) and some of its esters are secondary metabolites produced by species of Celastraceae family, which have being associated with cytotoxic activity. We report herein the isolation of 1, the semi-synthesis of eight lupeol esters and the evaluation of their in vitro activity against nine strains of cancer cells. The reaction of carboxylic acids with 1 and DIC/DMAP was used to obtain lupeol stearate (2), lupeol palmitate (3) lupeol miristate (4), and the new esters lupeol laurate (5), lupeol caprate (6), lupeol caprilate (7), lupeol caproate (8) and lupeol 3’,4’-dimethoxybenzoate (9), with high yields. Compounds 1-9 were identified using FT-IR, 1H, 13C-NMR, CHN analysis and XRD data and were tested in vitro for proliferation of human cancer cell activity. In these assays, lupeol was inactive (GI50> 250μg/ mL) while lupeol esters 2 -4 and 7 - 9 showed a cytostatic effect. The XRD method was a suitable tool to determine the structure of lupeol and its esters in solid state. Compound 3 showed a selective growth inhibition effect on erythromyeloblastoid leukemia (K-562) cells in a concentration-dependent way. Lupeol esters 4 and 9 showed a selective cytostatic effect with low GI50 values representing promising prototypes for the development of new anticancer drugs.