ISOLATION AND ANTITRICHOMONAL ACTIVITY OF THE CHEMICAL CONSTITUENTS OF THE LEAVES OF Maytenus phyllanthoides Benth. (Celastraceae)

被引:12
作者
Alberto Moo-Puc, Juan [1 ]
Martin-Quintal, Zhelmy [1 ]
Miron-Lopez, Gumersindo [1 ]
Esther Moo-Puc, Rosa [2 ]
Quijano, Leovigildo [3 ]
Mena-Rejon, Gonzalo J. [1 ]
机构
[1] Univ Autonoma Yucatan, Fac Quim, Quim Farmaceut Lab, Merida 97150, Yuc, Mexico
[2] Inst Mexicano Seguro Social, Ctr Med Ignacio Garcia Tellez, Unidad Med Alta Especialidad, Unidad Invest Med Yucatan, Merida 97150, Yuc, Mexico
[3] Univ Nacl Autonoma Mexico, Inst Quim, Coyoacan 04510, DF, Mexico
来源
QUIMICA NOVA | 2014年 / 37卷 / 01期
关键词
Maytenus phyllantoides; (+)-lyoniresinol; antitrichomonal activity; TRICHOMONAS-VAGINALIS; IN-VITRO; ENTAMOEBA-HISTOLYTICA; CINNAMOMUM-CASSIA; NATURAL-PRODUCTS; DISCOVERY; LIGNANS; BARK;
D O I
10.1590/S0100-40422014000100016
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cyclolignan (+)-lyoniresinol (1), veratric acid (2), vanillic acid (3), lupeol, oleanolic acid, 3 beta-hydroxy-urs-11-en-28,13 beta-lactone (4), the mixture of alpha- and beta-amyrin, trans-polyisoprene, and beta-sitosterol were isolated from the leaves of Maytenus phyllanthoides. The structures of the isolated compounds were established based on spectroscopic data, mainly H-1 and C-13 nuclear magnetic resonance (NMR). Compound 1, its acetate analog 1a, and compounds 2, 3, and 4 were tested against Trichomonas vaginalis. (+)-Lyoniresinol showed activity corresponding to IC50 17.57 mu M. This is the first report on the occurrence of 3 beta-hydroxy-urs-11-en-28,13 beta-lactone (4) in the Celastraceous family and lyoniresinol in the Maytenus genus, and on the antitrichomonal activity of lyoniresinol.
引用
收藏
页码:85 / U114
页数:14
相关论文
共 41 条
  • [1] Ahmad ViqarUddin., 1994, HDB NATURAL PRODUCTS, V2
  • [2] Current therapeutics, their problems, and sulfur-containing-amino-acid metabolism as a novel target against infections by "amitochondriate" protozoan parasites
    Ali, Vahab
    Nozaki, Tomoyoshi
    [J]. CLINICAL MICROBIOLOGY REVIEWS, 2007, 20 (01) : 164 - +
  • [3] Variability and variation in drug susceptibility among Giardia duodenalis isolates and clones exposed to 5-nitroimidazoles and benzimidazoles in vitro
    Argüello-García, R
    Cruz-Soto, M
    Romero-Montoya, L
    Ortega-Pierres, G
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2004, 54 (04) : 711 - 721
  • [4] Tyrosinase inhibitory lignans from the methanol extract of the roots of Vitex negundo Linn. and their structure-activity relationship
    Azhar-ul-Haq
    Malik, A
    Khan, MTH
    Anwar-ul-Haq
    Khan, SB
    Ahmad, A
    Choudhary, MI
    [J]. PHYTOMEDICINE, 2006, 13 (04) : 255 - 260
  • [5] The role of natural product chemistry in drug discovery
    Butler, MS
    [J]. JOURNAL OF NATURAL PRODUCTS, 2004, 67 (12): : 2141 - 2153
  • [6] Anti-Trichomonas vaginalis activity of Hypericum polyanthemum extract obtained by supercritical fluid extraction and isolated compounds
    Cargnin, Simone Tasca
    Vieira, Patricia de Brum
    Cibulski, Samuel
    Cassel, Eduardo
    Figueiro Vargas, Rubem Mario
    Montanha, Jarbas
    Roehe, Paulo
    Tasca, Tiana
    von Poser, Gilsane Lino
    [J]. PARASITOLOGY INTERNATIONAL, 2013, 62 (02) : 112 - 117
  • [7] In vitro effect of nitazoxanide against Entamoeba histolytica, Giardia intestinalis and Trichomonas vaginalis trophozoites
    Cedillo-Rivera, R
    Chávez, B
    González-Robles, A
    Tapia, A
    Yépez-Mulia, L
    [J]. JOURNAL OF EUKARYOTIC MICROBIOLOGY, 2002, 49 (03) : 201 - 208
  • [8] Clevinger C., 2010, FLORA VALLE TEHUACAN
  • [9] Anti-infective potential of natural products: How to develop a stronger in vitro 'proof-of-concept'
    Cos, Paul
    Vlietinck, Arnold J.
    Vanden Berghe, Dirk
    Maes, Louis
    [J]. JOURNAL OF ETHNOPHARMACOLOGY, 2006, 106 (03) : 290 - 302
  • [10] El-Domiaty M.M., 1999, ALEX J PHARM SCI, V13, P1