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Published byWillis Williams Modified over 8 years ago
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Mode of Action of Insecticides
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Classification: Chemical Insecticides –Arsenicals and inorganics-Botanicals –Carbamates-Diamides (pyrazoles) –Dinitrophenols-Formamidines –Fumigants-Benzoylureas –Juvenile hormones-Moulting hormones –Macrolides-Nereistoxin analogues Organochlorines –Neonicotinoids-Organochlorines Oxadiazine/diazoles –Organophosphorus-Oxadiazine/diazoles –Phthalimides-Pyrethroids –Pyrimidine amines-Pyrroles/Pyazoles –Tetramic acids –Tetramic acids-Thiazoles –Urea and thiourea-Miscellaneous
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Macrolides Neurotoxicant Cl-Channel blocker Abamectin & analogues Same MOA of Fipronil
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GABA-gated channels
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Nereistoxin analogues Natural insecticide nereistoxin from Lumbrineris heteropoda. Nereistoxin acts on nicotinic acetylcholine receptors, as partial agonist at low concentration and as channel blocker at higher concentration. Toxic to insects but not lethal to mammalians
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Structures
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Organochlorines Numerous sub-class Generally neurotoxicant Generally persistent in environment Various side-effects
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General structures Halogenated aryl compounds Halogenated cyclodienes DDT Lindane Aldrin Mirex Endosulfan
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Mode of action Same as fipronil, abamectin but different site of binding GABA-gated Cl-channel
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Oxadiazines/diazoles Neurotoxicant Voltage-dependent sodium channel blocker Indoxacarb Metoxadiazone
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Voltage-gated Cl-channel Important of potential propagation in neuron cells Na+ channels both open and close more quickly than K+ channels, producing an influx of positive charge (Na+) toward the beginning of the action potential and an efflux (K+) toward the end.
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Pyrimidine amines Mitochondrial complex I electron transport inhibitor Pyrimidifen
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MOA of Pyrimidine amines
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Pyrroles/Pyrazoles Fipronil: Neurotoxicant, GABA-Cl channel Chlorfenapyr: –Chlorfenapyr has a unique mode of action. It is a pro-insecticide that is converted (or metabolized) to the active form by mixed function oxidases (MFOs) in the target pest. The active form acts on the mitochondria and uncouples oxidative phosphorylation which stops the production of ATP, the primary source of cellular energy.
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General structures Pyrroles Chlorfenapyr Pyrazoles Fipronil Pyrazoles Vaniliprole
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Metabolic transformation Chlorfenapyr De-Ethoxymethylation
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Oxidative phosphorylation
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Tetramic/Tetronic acids Its mode of action is by inhibition of lipid biosynthesis that affects the egg and immature stages of these pests. acetyl-CoA-carboxylase, a lipid metabolism enzyme,16 and causes a significant decrease in total lipids. Tetramic acid Spirotetramet Tetronic acid Spiromesifen
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Lipid biosynthesis and AcCoA carboxylase
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Urea and Thiourea Urea: Chitin biosynthesis inhibitor Thiourea: ATP synthase inhibitor Urea Sulcofuron Thiourea Diafenthiuron
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Metabolic change of activity
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Miscellaneous Insecticides Fenoxacrim: Maybe SDH inhibitor Hydramethylnon: ATP biosynthesis Isoprothiolane: Lipid biosynthesis inhibitor: insecticide and fungicide Triazamate: Maybe acetylcholine esterase inhibitor
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Structures Isoprothiolane Fenoxacrim Hydramethylnon Triazamate
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