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![Page 1: New Insecticide Modes of Action: Whence Selectivity? Joel Coats Professor of Entomology and Toxicology Iowa State University Ames, Iowa.](https://reader036.fdocuments.in/reader036/viewer/2022062308/56649d765503460f94a573c6/html5/thumbnails/1.jpg)
New Insecticide New Insecticide Modes of Action:Modes of Action:
Whence Selectivity?Whence Selectivity?
Joel CoatsJoel Coats
Professor of Entomology and ToxicologyProfessor of Entomology and Toxicology
Iowa State UniversityIowa State University
Ames, IowaAmes, Iowa
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Outline Selectivity New Insecticide Classes
Neonictinoids Fipronil Chlorphenapyr Sulfluramid Spinosads Buprofezin Diafenthiauron Indoxacarb Metaflumazone Pymetrozine
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Where have we been?Where have we been?
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CHCl
CCl3
Cl
DDT
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O
Cl
ClCl
Cl
Cl
Cl
dieldrin
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Cl
Cl
ClCl
Cl
Cl
lindane
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Where are we now, Where are we now, and where are we headed?and where are we headed?
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NeonicotinoidsNeonicotinoids
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NCl
N
NH
NNo2
Imidacloprid
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Mode of Action
•Binds irreversibly to postsynaptic nicotinic acetlycholine receptors.
ImidaclopridImidacloprid
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NeoNeo
ACHACH
NERVE SYNAPSENERVE SYNAPSE
nerve axonnerve axon
NeoNeo
Neonicotinoid: Acetylcholine AgonistNeonicotinoid: Acetylcholine AgonistNeonicotinoid: Acetylcholine AgonistNeonicotinoid: Acetylcholine Agonist
ACH
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NeonicotinoidsNeonicotinoidsThiamethoxamThiamethoxam
Control wide range of Control wide range of sucking / chewing sucking / chewing pests like aphids, pests like aphids, thrips, termites, thrips, termites, weevils, beetles, weevils, beetles, wireworms, fire antswireworms, fire ants
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Toxicity to non-targetsToxicity to non-targets Rat oral LDRat oral LD5050 a.i. = 1,563 mg/kg a.i. = 1,563 mg/kg
Rat dermal LDRat dermal LD5050 a.i. >2,000 mg/kg a.i. >2,000 mg/kg
Water solubility = 4,100 mg/LWater solubility = 4,100 mg/L
Neonicotinoids--ThiamethoxamNeonicotinoids--Thiamethoxam
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FipronilFipronil
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fipronil - Regentfipronil - Regent
Phenyl-pyrazole family
fipronil - primary fipronil - primary family member in family member in productionproduction
F3C Cl
ClN
N CN
SH2N
F3CO
Fipronil
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Fipronil Mode of ActionFipronil Mode of Action
Acts as an inhibitor at the Acts as an inhibitor at the -aminobutyric -aminobutyric acid (GABA) receptor as a noncompetitive acid (GABA) receptor as a noncompetitive blocker of the GABA-gated chloride blocker of the GABA-gated chloride channel (similar to lindane and channel (similar to lindane and cyclodienes)cyclodienes)
Chemical and biological activation Chemical and biological activation producing equally toxic and sometime more producing equally toxic and sometime more persistent metabolites with same mode of persistent metabolites with same mode of actionaction
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Cl- K+
Cl-
Cl-Cl-
GABA-gated Chloride Channel GABA-gated Chloride Channel
Nerve AxonNerve AxonNerve AxonNerve Axon
Na+
Cl-
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Fipr
K+
Cl-
Cl-Cl-
Antagonist at GABA-gated Chloride Channel Antagonist at GABA-gated Chloride Channel
Fipronil Mode of ActionFipronil Mode of ActionFipronil Mode of ActionFipronil Mode of Action
Na+
Cl-
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Selective Toxicity of FipronilSelective Toxicity of Fipronil
Vertebrate
Acute Mouse Oral LD50 = 41 mg/kg
Insect
Acute Housefly Contact LD50 = 0.13 mg/kg
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ChlorfenapyrChlorfenapyr
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Chlorfenapyr, AC-303,630
ChlorfenapyrChlorfenapyr
American Cyanamid American Cyanamid product, now BASFproduct, now BASF
Registered outside U.S. Registered outside U.S. for cottonfor cotton
Broad-spectrum Broad-spectrum insecticidal actioninsecticidal action
N
CH2
Br
F3C
CH3
ClO
C2H5
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ChlorfenapyrChlorfenapyrOxidative PhosphorylationOxidative Phosphorylation
Chemiosmotic theory
Electron flow through the electron transport chain is accompanied by a transfer of protons
ATP synthesis driven by proton-motive force
Electron transport train uses O2 as final electron receptor
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SulfluramidSulfluramid
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CH3CH2 N S C C C C CCC
O
O
H
F
F F F F F F F
F F F F F F
CF3
sulfluramid
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SpinosadsSpinosads
New class of potent natural New class of potent natural insecticidesinsecticides
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O
N
R
R1
HO
O
O
OR5
H H
R6
R7
H H O OH
OR4
OR3
R2O
SPINOSADS
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SpinosadsSpinosads
Mode of action – acts on the acetylcholine Mode of action – acts on the acetylcholine receptor to make it more excitable receptor to make it more excitable Overstimulation of the nerve results.Overstimulation of the nerve results.
Hypothesis currently considered most Hypothesis currently considered most plausible, although not really accepted as plausible, although not really accepted as the last wordthe last word
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ACHACH
ACHACH
ACHACH
ACHACH
NERVE SYNAPSENERVE SYNAPSE
nerve axonnerve axon
Acetylcholine Receptor - SpinosadsAcetylcholine Receptor - SpinosadsAcetylcholine Receptor - SpinosadsAcetylcholine Receptor - Spinosads
Spyn
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N
N
S
O
NC(CH3)3
CH(CH3)2
buprofezin
Buprofezin
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Buprofezin – Mode of ActionBuprofezin – Mode of Action
Inhibits chitin synthesis/depositionInhibits chitin synthesis/deposition
Effect similar to benzoyl phenylureasEffect similar to benzoyl phenylureas
Insects die when newly moltedInsects die when newly molted
IGRIGR
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DiafenthiuronDiafenthiuron
O
CH(CH3)2
CH(CH3)2
HN C
S
NHC(CH3)3
diafenthiuron
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Diafenthiuron- Mode of ActionDiafenthiuron- Mode of Action
Inhibits ATPase in mitochondriaInhibits ATPase in mitochondria
Blocks utilization of energy (ATP)Blocks utilization of energy (ATP)
Thiourea compoundThiourea compound
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IndoxacarbIndoxacarb
O
N
N
C
OOCH3
N OCH3
OO
OCF3
Cl
indoxacarb
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Indoxacarb – Mode of ActionIndoxacarb – Mode of Action
Blocks sodium channel in nerve axonBlocks sodium channel in nerve axon
Inhibits propagation of nerve potentialInhibits propagation of nerve potential
Oxadiazine compoundOxadiazine compound
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Indox
Na+Na+
K+
Cl-
Cl-Cl-
Nerve Potential PropagationNerve Potential Propagation
Indoxacarb effect on nerve axonIndoxacarb effect on nerve axonIndoxacarb effect on nerve axonIndoxacarb effect on nerve axon
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Metaflumizone
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MetaflumizoneMetaflumizone
Putative mode of action – blocks sodium Putative mode of action – blocks sodium channel in nerveschannel in nerves
Log P 4.7-5.4Log P 4.7-5.4
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PymetrozinePymetrozine
HN
N
N
N
O
N
pymetrozine
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Pymetrozine – Mode of ActionPymetrozine – Mode of Action
Inhibits feeding of sucking insectsInhibits feeding of sucking insects
Especially active on aphidsEspecially active on aphids
Pyridine azomethine compoundPyridine azomethine compound
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ConclusionsConclusions
A number of very new classes of A number of very new classes of insecticides have been developed, with insecticides have been developed, with new modes of action.new modes of action.
Availability of products is changing, toward Availability of products is changing, toward newer classes of insecticides. newer classes of insecticides.
Selectivity is ever more important:Selectivity is ever more important:
to applicators, to livestock, pets, wildlife, to applicators, to livestock, pets, wildlife, environment, residues in food.environment, residues in food.
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ConclusionsConclusions
Some of the new chemistry perpetuates Some of the new chemistry perpetuates non-selective insecticide toxicity.non-selective insecticide toxicity.
Some of it allows opportunities for safer, Some of it allows opportunities for safer, more selective insecticides.more selective insecticides.
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QuestionsQuestions
How many and which modes of action How many and which modes of action should be screened for in non-target should be screened for in non-target bioassays? High throughput assays?bioassays? High throughput assays?
Can we predict which species will be most Can we predict which species will be most vulnerable and under what exposure vulnerable and under what exposure (conc., timing)?(conc., timing)?
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The First McKim Conference: The First McKim Conference: Some Important QuestionsSome Important Questions
Best bioassays?Best bioassays?
Specificity and selectivity?Specificity and selectivity?
Extrapolation?Extrapolation?
Metabolic detoxification or activation?Metabolic detoxification or activation?
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““If you’re not part of the solution…If you’re not part of the solution…you’re part of the precipitate.”you’re part of the precipitate.”
- Anon (C&EN)- Anon (C&EN)
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Getting answers depends on Getting answers depends on the quality of “the hired help.”the quality of “the hired help.”
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Steve Bradbury, circa 1984Steve Bradbury, circa 1984
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PartPart of Jim McKim’s rich legacyof Jim McKim’s rich legacy
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