Journal of Pesticide Science · 2015 · 36 citations · 2 references
Life SciencesBiochemistryPharmacologyEnzymologyMetabolismMitochondrial BiologyEnzyme InhibitionMitochondrial BiochemistryMitochondrial BioenergeticsMitochondrial FunctionMitochondrial MetabolismRespiration InhibitionAcaricide ChemistryMitochondrial Enzyme InhibitionMitochondrial Respiration InhibitionMitochondrial Respiratory Chain InhibitionMitochondrial Respiratory Chain ToxicityMitochondrial Respiratory Complex IiRespiratory Enzyme InhibitionRespiratory Inhibition Mechanisms
This study aimed to determine the mode of action of pyflubumide, a novel acaricide under development by Nihon Nohyaku Co., Ltd. Because of its structural similarity to succinate-dehydrogenase inhibitor (SDHI) fungicides, its ability to inhibit mitochondrial complex II was investigated. Pyflubumide exhibited low inhibitory activity on spider mite mitochondria; conversely, its deacylated metabolite (NH-form) showed high mitochondrial inhibitory activity. Pyflubumide was quickly metabolized to its NH-form in the homogenate of spider mites. These results suggest that pyflubumide is a prodrug and that the NH-form is active. Indeed, the NH-form of pyflubumide and the OH-form of cyenopyrafen, a complex II inhibitory acaricide, act on the same enzyme; a double-inhibitor titration assay showed that the binding sites on mitochondrial complex II and/or the manners of binding of these compounds exhibit clear differences. This finding suggests that these two acaricides should be classified into different groups in terms of their mode of action.
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Cyflumetofen, a novel acaricide – its mode of action and selectivity
Naotaka Hayashi, Yasuhiro Sasama, Nobuyoshi Takahashi et al. · Pest Management Science · 2012 · 110 citations