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1.
Parasitol Res ; 112(2): 511-6, 2013 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-23064801

RESUMO

The larvicidal activity of crude petroleum ether, toluene, n-butanol, ethyl acetate, acetone, and methanol extracts of the seeds of Clausena lansium was assayed for their toxicities against the early fourth instar larvae of Aedes albopictus. The larval mortality was observed after 24-h exposure. The LC(50) value of petroleum ether extract was 22.99 ppm, showing the best larvicidal activity among all six solvent extracts. A cinnamon amide compound lansiumamide B (N-methyl-N-cis-styrylcinnamamide) was isolated from the petroleum ether extract by column chromatographic method, which exhibited a strong larvicidal activity against the early fourth instar larvae of A. albopictus with LC(50) and LC(90) values of 0.45 and 2.19 ppm, respectively. The structure was elucidated by (1)H NMR, (13)C NMR spectral data. The larvicidal activity against mosquito of lansiumamide B from the seed of C. lansium was evaluated for the first time.


Assuntos
Aedes/efeitos dos fármacos , Cinamatos/farmacologia , Clausena/química , Inseticidas/farmacologia , Extratos Vegetais/farmacologia , Estirenos/farmacologia , Animais , Cromatografia Líquida , Cinamatos/química , Cinamatos/isolamento & purificação , Inseticidas/química , Inseticidas/isolamento & purificação , Larva/efeitos dos fármacos , Espectroscopia de Ressonância Magnética , Extratos Vegetais/química , Extratos Vegetais/isolamento & purificação , Sementes/química , Estirenos/química , Estirenos/isolamento & purificação , Análise de Sobrevida
2.
Environ Entomol ; 48(1): 147-155, 2019 02 13.
Artigo em Inglês | MEDLINE | ID: mdl-30508198

RESUMO

Entomopathogenic fungi (EPF), such as Metarhizium spp. and Beauveria bassiana, are widely used in the biocontrol of many species of insect pests. Tobacco is an economically important crop in Guangdong Province of China, but insect pests, such as Spodoptera litura Fabricius, are a major threat to production. Here, we tested the persistence of five Metarhizium species and B. bassiana in glasshouse pot and field experiments and assessed their long-term efficacy against S. litura. We found that the colony forming units of these EPF decreased by c. 93% by 180 d in the pot soils declines tended to be exponential. In contrast, declines of c. 99% in field soils were more gradual (linear), occurring throughout the 360 d experiment. Metarhizium anisopliae Ma09 had the longest estimated half-life of 41 d, while that of B. bassiana was the shortest (9 d). Fungal density in the upper soil layer (0-5 cm) decreased rapidly and was undetectable after 150 d, whereas density was consistently greatest in the mid-layer (10-15 cm). At 180 d after inoculation, strain Ma09 elicited highest rates of mortality in S. litura. We conclude that soils in Guangdong Province are all suitable for the use of Metarhizium as a biocontrol agent, where M. anisopliae Ma09 offers greatest residual activity.


Assuntos
Beauveria/fisiologia , Metarhizium/fisiologia , Controle Biológico de Vetores , Microbiologia do Solo , Spodoptera , Animais , China , Pupa , Esporos Fúngicos/fisiologia , Nicotiana
3.
J Agric Food Chem ; 59(9): 4801-13, 2011 May 11.
Artigo em Inglês | MEDLINE | ID: mdl-21452831

RESUMO

On the basis of the previous work for optimization of O,O-diethyl α-(substituted phenoxyacetoxy)alkylphosphonates, further extensive synthetic modifications were made to the substituents in alkylphosphonate and phenoxy moieties of the title compounds. New O,O-dimethyl α-(substituted phenoxyacetoxy)alkylphosphonates were synthesized as potential inhibitors of pyruvate dehydorogenase complex (PDHc). Their herbicidal activity and efficacy in vitro against PDHc were examined. Some of these compounds exhibited significant herbicidal activity and were demonstrated to be effective inhibitors of PDHc from three different plants. The structure-activity relationships of these compounds including previously reported analogous compounds were studied by examining their herbicidal activities. Both inhibitory potency against PDHc and herbicidal activity of title compounds could be increased greatly by optimizing substituent groups of the title compounds. O,O-Dimethyl α-(2,4-dichlorophenoxyacetoxy)ethylphosphonate (I-5), which acted as a competitive inhibitor of PDHc with much higher inhibitory potency against PDHc from Pisum sativum and Phaseolus radiatus than from Oryza sativa , was found to be the most effective compound against broadleaf weeds and showed potential utility as herbicide.


Assuntos
Inibidores Enzimáticos/síntese química , Inibidores Enzimáticos/farmacologia , Herbicidas/síntese química , Herbicidas/farmacologia , Proteínas de Plantas/antagonistas & inibidores , Complexo Piruvato Desidrogenase/antagonistas & inibidores , Inibidores Enzimáticos/química , Herbicidas/química , Estrutura Molecular , Proteínas de Plantas/metabolismo , Plantas/efeitos dos fármacos , Plantas/enzimologia , Complexo Piruvato Desidrogenase/metabolismo , Relação Estrutura-Atividade
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