Please use this identifier to cite or link to this item: http://www.repositorio.ufop.br/handle/123456789/3853
Title: New triterpenes from Maytenus robusta : structural elucidation based on NMR experimental data and theoretical calculations.
Authors: Sousa, Grasiely Faria de
Duarte, Lucienir Pains
Alcântara, Antônio Flávio de Carvalho
Silva, Grácia Divina de Fátima
Vieira Filho, Sidney Augusto
Miranda, Roqueline Rodrigues Silva de
Oliveira, Djalma Menezes de
Takahashi, Jacqueline Aparecida
Keywords: Maytenus robusta
Pentacyclic triterpenes
Acetylcholinesterase inhibitory activity
Issue Date: 2012
Citation: SOUSA, G. F. de et al. New triterpenes from Maytenus robusta : structural elucidation based on NMR experimental data and theoretical calculations. Molecules, v. 17, p. 13439-13456, 2012. Disponível em: <http://www.mdpi.com/1420-3049/17/11/13439> Acesso em: 20 ago. 2014.
Abstract: Leaves of Maytenus robusta (Celastraceae) were subjected to phytochemical investigation mainly directed at the isolation of pentacyclic triterpenes. The compounds friedelin (1), β-friedelinol (2), 3-oxo-21β-H-hop-22(29)-ene (7), 3,4-seco-friedelan-3,11β- olide (8), 3β-hydroxy-21β-H-hop-22(29)-ene (9), 3,4-seco-21β-H-hop-22(29)-en-3-oic acid (10), 3,4-seco-friedelan-3-oic acid (11), and sitosterol were identified in the hexane extract of M. robusta leaves. Compounds 8 and 9 are described herein for the first time. The structure and stereochemistry of both compounds were experimentally established by IR, HRLC-MS, and 1D (1H, 13C, and DEPT 135) and 2D (HSQC, HMBC and COSY) NMR data and supported by correlations with carbon chemical shifts calculated using the DFT method (BLYP/6-31G* level). Compounds 7 and 10 are also described for the first time, and their chemical structures were established by comparison with NMR data of similar structures described in the literature and correlations with BLYP/6-31G* calculated carbon chemical shifts. Compound 9, a mixture of 11 and sitosterol, and 3β,11β-dihydroxyfriedelane (4) were evaluated by the Ellman’s method and all these compounds showed acethylcholinesterase inhibitory properties.
URI: http://www.repositorio.ufop.br/handle/123456789/3853
metadata.dc.identifier.doi: https://doi.org/10.3390/molecules171113439
ISSN: 1420-3049
metadata.dc.rights.license: This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Fonte: Molecules <http://www.mdpi.com/1420-3049/18/8/9919> Acesso em: 08 set. 2014.
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