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1.
Planta Med ; 78(14): 1601-6, 2012 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-22814822

RESUMO

Plants are promising sources of new bioactive compounds. The aim of this study was to investigate the cytotoxic potential of nine plants found in Brazil. The species studied were: Annona pickelii Diels (Annonaceae), Annona salzmannii A. DC. (Annonaceae), Guatteria blepharophylla Mart. (Annonaceae), Guatteria hispida (R. E. Fr.) Erkens & Maas (Annonaceae), Hancornia speciosa Gomes (Apocynaceae), Jatropha curcas L. (Euphorbiaceae), Kielmeyera rugosa Choisy (Clusiaceae), Lippia gracilis Schauer (Verbenaceae), and Hyptis calida Mart. Ex Benth (Lamiaceae). Different types of extractions from several parts of plants resulted in 43 extracts. Their cytotoxicity was tested against HCT-8 (colon carcinoma), MDA-MB-435 (melanoma), SF-295 (glioblastoma), and HL-60 (promielocitic leukemia) human tumor cell lines, using the thiazolyl blue test (MTT) assay. The active extracts were those obtained from G. blepharophylla, G. hispida, J. curcas, K. rugosa, and L. gracilis. In addition, seven compounds isolated from the active extracts were tested; among them, ß-pinene found in G. hispida and one coumarin isolated from K. rugora showed weak cytotoxic activity. In summary, this manuscript contributes to the understanding of the potentialities of Brazilian plants as sources of new anticancer drugs.


Assuntos
Compostos Bicíclicos com Pontes/farmacologia , Cumarínicos/farmacologia , Magnoliopsida/química , Monoterpenos/farmacologia , Óleos Voláteis/farmacologia , Extratos Vegetais/farmacologia , Annonaceae/química , Antineoplásicos Fitogênicos , Apocynaceae/química , Monoterpenos Bicíclicos , Brasil , Compostos Bicíclicos com Pontes/química , Compostos Bicíclicos com Pontes/isolamento & purificação , Linhagem Celular Tumoral , Sobrevivência Celular , Clusiaceae/química , Cumarínicos/química , Cumarínicos/isolamento & purificação , Humanos , Hyptis/química , Jatropha/química , Látex/química , Lippia/química , Monoterpenos/química , Monoterpenos/isolamento & purificação , Óleos Voláteis/química , Óleos Voláteis/isolamento & purificação , Componentes Aéreos da Planta/química , Extratos Vegetais/química , Extratos Vegetais/isolamento & purificação , Plantas Medicinais/química
2.
J Nat Med ; 66(3): 428-34, 2012 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-22146971

RESUMO

Lippia gracilis Schauer is an aromatic plant widely found in Northeastern Brazil. The leaf infusions or decoctions and alcoholic macerate are used for some inflammatory diseases and headache. This paper reports the isolation of naringenin by semi-preparative liquid chromatography from the methanolic extract of L. gracilis (ELg) and the evaluation of the analgesic and anti-inflammatory activities of this extract by measuring nociception through acetic acid, formalin, and hot-plate tests in carrageenan-induced inflammation in mice. Following oral administration, ELg (100, 200, and 400 mg/kg) significantly reduced the number of writhes in the writhing test and the time of paw licks in both phases of the formalin test when compared to the control group animals. Mice treated with ELg did not exhibit any behavioral alteration during the hot plate and rota-rod tests, suggesting non-participation of the supraspinal components in the modulation of pain by ELg and no motor abnormality. The oral administration of 400 mg/kg of ELg produced an anti-inflammatory effect on peritonitis induced by carrageenan. These effects can be associated with a decrease of inflammatory mediator synthesis by compounds of ELg, such as naringenin, which has anti-inflammatory action as already described.


Assuntos
Analgésicos/uso terapêutico , Anti-Inflamatórios/uso terapêutico , Lippia/química , Dor/tratamento farmacológico , Extratos Vegetais/uso terapêutico , Analgésicos/química , Animais , Anti-Inflamatórios/química , Brasil , Masculino , Camundongos , Extratos Vegetais/química
3.
Bioorg Med Chem Lett ; 14(9): 2199-204, 2004 May 03.
Artigo em Inglês | MEDLINE | ID: mdl-15081008

RESUMO

3D QSAR studies were performed on a library of 120 GAPDH inhibitors, including a series of coumarins, flavonoids, and nucleosides. The VolSurf method was successfully used to calculate surface descriptors for protein-ligand affinity and binding site of the enzyme. PCA/PLS analyses have permitted the evaluation of the structural features crucial for potency, selectivity, and favorable pharmacokinetic properties, and are important for the design of new ligands.


Assuntos
Inibidores Enzimáticos/química , Inibidores Enzimáticos/farmacologia , Gliceraldeído 3-Fosfato Desidrogenase (NADP+)/antagonistas & inibidores , Inibidores Enzimáticos/farmacocinética , Relação Quantitativa Estrutura-Atividade
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