Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
J Agric Food Chem ; 52(12): 3884-7, 2004 Jun 16.
Artigo em Inglês | MEDLINE | ID: mdl-15186111

RESUMO

The gamma-aminobutyric acid (GABA) receptor bears sites of action for insecticides. To discover GABA receptor-directed insecticides in natural products, fungal culture extracts were screened for their ability to inhibit specific binding of the radiolabeled noncompetitive antagonist [3H]1-(4-ethynylphenyl)-4-n-propyl-2,6,7-trioxabicyclo[2.2.2]octane to housefly head membranes. The screening efforts led to the isolation of two alkaloids from Aspergillus terreus: PF1198A (alantrypinone) and PF1198B (serantrypinone), which had IC50 values of 0.34 and 2.1 microM, respectively, in this assay. These compounds were ca. 47-61-fold selective for housefly vs rat GABA receptors. Both compounds showed insecticidal activity against Myzus persicae in the range of 100-500 ppm. Binding assay-guided screening should provide significant opportunities for the identification of novel and selective insecticides.


Assuntos
Inseticidas/isolamento & purificação , Receptores de GABA/metabolismo , Alcaloides/química , Alcaloides/isolamento & purificação , Animais , Aspergillus/metabolismo , Química Encefálica , Compostos Bicíclicos Heterocíclicos com Pontes/antagonistas & inibidores , Compostos Bicíclicos Heterocíclicos com Pontes/metabolismo , Membrana Celular/química , Antagonistas GABAérgicos/química , Antagonistas GABAérgicos/isolamento & purificação , Moscas Domésticas , Indóis/química , Indóis/isolamento & purificação , Quinazolinas/química , Quinazolinas/isolamento & purificação , Ratos , Trítio
2.
Bioorg Med Chem ; 10(6): 1873-81, 2002 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-11937345

RESUMO

Thirteen seco-prezizaane terpenoids isolated from star anise species (Illcium floridanum, Illcium parviflorum, and Illcium verum) were investigated for their ability to inhibit the specific binding of [(3)H]4'-ethynyl-4-n-propylbicycloorthobenzoate (EBOB), a non-competitive antagonist of gamma-aminobutyric acid (GABA) receptors, to housefly-head and rat-brain membranes. Veranisatin A was found to be the most potent inhibitor in both membranes, with an IC(50)(fly) of 78.5 nM and an IC(50)(rat) of 271 nM, followed by anisatin (IC(50)(fly)=123 nM; IC(50)(rat)=282 nM). Six of the other 11 tested compounds were effective only in housefly-head membranes. Pseudoanisatin proved to display a high (>26-fold) selectivity for housefly versus rat GABA receptors (IC(50)(fly)=376 nM; IC(50)(rat) >10,000 nM). Although pseudoanisatin does not structurally resemble EBOB, Scatchard plots indicated that the two compounds bind to the same site in housefly receptors. Anisatin and pseudoanisatin exhibited moderate insecticidal activity against German cockroaches. Comparative molecular field analysis (CoMFA), a method of three-dimensional quantitative structure-activity relationship (3D-QSAR) analysis, demonstrated that seco-prezizaane terpenoids can bind to the same site as do picrotoxane terpenoids such as picrotoxinin and picrodendrins, and the CoMFA maps allowed us to identify the parts of the molecules essential to high activity in housefly GABA receptors.


Assuntos
Antagonistas GABAérgicos/química , Antagonistas GABAérgicos/farmacologia , Receptores de GABA/metabolismo , Terpenos/química , Terpenos/farmacologia , Animais , Ligação Competitiva , Encéfalo/citologia , Encéfalo/efeitos dos fármacos , Encéfalo/metabolismo , Membrana Celular/efeitos dos fármacos , Membrana Celular/metabolismo , Baratas/efeitos dos fármacos , Relação Dose-Resposta a Droga , Cabeça , Moscas Domésticas , Concentração Inibidora 50 , Inseticidas/química , Inseticidas/farmacologia , Modelos Moleculares , Conformação Molecular , Estrutura Molecular , Ratos , Relação Estrutura-Atividade
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...