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Sci Rep ; 6: 22977, 2016 Mar 10.
Artigo em Inglês | MEDLINE | ID: mdl-26960713


A pair of chemical isomeric structures of novel N-tert-butylphenyl thenoylhydrazide compounds I and II were designed and synthesized. Their structures were characterized by MS, IR, (1)H NMR, elemental analysis and X-ray single crystal diffraction. The regioselectivity of the Meerwein arylation reaction and the electrophilic substitution reaction of N-tert-butyl hydrazine were studied by density functional theory (DFT) quantum chemical method. The larvicidal tests revealed that some compounds I had excellent larvicidal activity against Culex pipiens pallens. As the candidates of insect growth regulators (IGRs), the larval growth inhibition and regulation against Culex pipiens pallens were examined for some compounds, especially I1 and I7. Compounds I1 and I7 were further indicated as an ecdysteroid agonist by reporter gene assay on the Spodoptera frugiperda cell line (Sf9 cells). Finally, a molecular docking study of compound I7 was conducted, which was not only beneficial to understand the structure-activity relationship, but also useful for development of new IGRs for the control of mosquitos.

Hidrazinas/química , Inseticidas/química , Hormônios Juvenis/química , Larva/efeitos dos fármacos , Animais , Culex/efeitos dos fármacos , Culex/patogenicidade , Humanos , Hidrazinas/síntese química , Hidrazinas/farmacologia , Inseticidas/síntese química , Inseticidas/farmacologia , Hormônios Juvenis/síntese química , Hormônios Juvenis/farmacologia , Espectroscopia de Ressonância Magnética , Simulação de Acoplamento Molecular , Spodoptera/efeitos dos fármacos , Spodoptera/patogenicidade , Relação Estrutura-Atividade