Brazoides A-D, New Alkaloids from Justicia gendarussa Burm. F. Species

被引:10
|
作者
Souza, Luciana G. S. [1 ]
Almeida, Macia C. S. [1 ]
Lemos, Telma L. G. [1 ]
Ribeiro, Paulo R. V. [2 ]
Canuto, Kirley M. [2 ]
Braz-Filho, Raimundo [3 ,4 ]
Del Cistia, Catarina N. [5 ]
Sant'Anna, Carlos Mauricio R. [6 ]
Barreto, Francisco S. [7 ]
de Moraes, Manoel O. [7 ]
机构
[1] Univ Fed Ceara, Dept Quim Organ & Inorgan, BR-60451970 Fortaleza, Ceara, Brazil
[2] Embrapa Agroind Trop, BR-60511110 Fortaleza, Ceara, Brazil
[3] Univ Fed Rural Rio de Janeiro, ICE, Dept Quim, FAPERJ, BR-23890000 Seropedica, RJ, Brazil
[4] Univ Estadual Norte Fluminense, Lab Ciencias Quim, BR-28035200 Campos Dos Goytacazes, RJ, Brazil
[5] Univ Fed Rural Rio de Janeiro, ICE, Dept Matemat, BR-23894374 Seropedica, RJ, Brazil
[6] Univ Fed Rural Rio de Janeiro, ICE, Dept Quim, BR-23894374 Seropedica, RJ, Brazil
[7] Univ Fed Ceara, NPDM, BR-60430275 Fortaleza, Ceara, Brazil
关键词
Acanthaceae; Justicia gendarussa; alkaloids; Brazoides; MEDICINAL-PLANTS;
D O I
10.21577/0103-5053.20160291
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Four new alkaloids, Brazoides A-D, together with three known compounds squalene, beta-sitosterol and lupeol, were isolated from leaves of Justicia gendarussa. These structures were established by spectrometric techniques, mainly high-resolution electrospray ionization mass spectrometry (HRESIMS) and 1D and 2D nuclear magnetic resonance (NMR), including comparative analysis with literature values. Structural determination of the compounds, Brazoides A-D, was strengthened by molecular modeling and density functional theory (DFT) calculations to predict the NMR data and compare with the experimental NMR values of these natural products. The new compounds were tested against three human cancer cell lines (glioblastoma, prostate and colon), but none exhibited activity.
引用
收藏
页码:1281 / 1287
页数:7
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