U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS
Clorfenvinfos (chlorfenvinphos) is an organophosphate insecticide, which is used to control insect pests on livestock, and to control household pests such as flies, fleas, and mites. Clorfenvinfos was sold under trade names including Birlane®, Dermaton®, Sapercon®, Steladone®, and Supona®. In 1991 all products containing clorfenvinfos were banned in the USA. Toxicity of clorfenvinfos is due to inhibition of acetylcholinesterase. Inhibition of cholinesterase activity results in the accumulation of acetylcholine at muscarinic and nicotinic receptors. This leads to continuous or excessive stimulation of cholinergic fibers in the post-ganglionic parasympathetic nerve endings, neuromuscular junctions of the skeletal muscles, resulting in hyperpolarization of nerve or muscle fibers and receptor desensitization until hydrolysis of the phosphorylated cholinesterase occurs. In some cases, a dealkylation and stabilization of the phosphorylated enzyme (“aging”) occur such that hydrolysis can no longer take place and the enzyme is irreversibly inhibited. In such cases, the return of acetylcholinesterase activity parallels the time required to resynthesize this enzyme.

Approval Year

PubMed

PubMed

TitleDatePubMed
Effects of insecticides in vitro and in vivo on esterase-6 in Drosophila melanogaster.
1978
Neurochemical alterations in rat brain as a test for studying the neurotoxicity of organophosphorus insecticides.
1980
Pretreatment of rats with an organophosphorus insecticide, chlorfenvinphos, protects against subsequent challenge with the same compound.
1990 Apr
Differences in the mode of lethality produced through intravenous and oral administration of organophosphorus insecticides in rats.
1991 Apr
Reactivation by various oximes of human erythrocyte acetylcholinesterase inhibited by different organophosphorus compounds.
1996
On the interactions between antimuscarinic atropine and NMDA receptor antagonists in anticholinesterase-treated mice.
2001 Jan
Amphetamine- and scopolamine-induced locomotor activity following treatment with chlorphenvinphos or chlorphyriphos in rats.
2005
Differential protein adduction by seven organophosphorus pesticides in both brain and thymus.
2007 Apr
Esterase metabolism of cholinesterase inhibitors using rat liver in vitro.
2011 Mar 15
A concentration addition model to assess activation of the pregnane X receptor (PXR) by pesticide mixtures found in the French diet.
2014 Sep
Patents
Substance Class Mixture
Created
by admin
on Sat Dec 16 15:39:56 GMT 2023
Edited
by admin
on Sat Dec 16 15:39:56 GMT 2023
Record UNII
F2G9XS1W91
Record Status Validated (UNII)
Record Version
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Name Type Language
CHLORFENVINPHOS
Common Name English
SD-7859
Code English
CLOFENVINPHOS
HSDB   ISO   MI  
Common Name English
clofenvinfos [INN]
Common Name English
SUPONA
Brand Name English
CHLORFENVINPHOS [HSDB]
Common Name English
SD 7859
Code English
CLOFENVINFOS
INN   MART.  
INN  
Official Name English
2-CHLORO-1-(2,4-DICHLOROPHENYL)VINYL DIETHYL PHOSPHATE
Systematic Name English
CLOFENVINFOS [MART.]
Common Name English
CHLORFENVINPHOS [ISO]
Common Name English
CHLORFENVINPHOS [MI]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 84101
Created by admin on Sat Dec 16 15:39:56 GMT 2023 , Edited by admin on Sat Dec 16 15:39:56 GMT 2023
Code System Code Type Description
ECHA (EC/EINECS)
207-432-0
Created by admin on Sat Dec 16 15:39:56 GMT 2023 , Edited by admin on Sat Dec 16 15:39:56 GMT 2023
PRIMARY
EPA CompTox
DTXSID7034250
Created by admin on Sat Dec 16 15:39:56 GMT 2023 , Edited by admin on Sat Dec 16 15:39:56 GMT 2023
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ALANWOOD
chlorfenvinphos
Created by admin on Sat Dec 16 15:39:56 GMT 2023 , Edited by admin on Sat Dec 16 15:39:56 GMT 2023
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MESH
D002709
Created by admin on Sat Dec 16 15:39:56 GMT 2023 , Edited by admin on Sat Dec 16 15:39:56 GMT 2023
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PUBCHEM
10107
Created by admin on Sat Dec 16 15:39:56 GMT 2023 , Edited by admin on Sat Dec 16 15:39:56 GMT 2023
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ChEMBL
CHEMBL2104653
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CHEBI
38598
Created by admin on Sat Dec 16 15:39:56 GMT 2023 , Edited by admin on Sat Dec 16 15:39:56 GMT 2023
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HSDB
1540
Created by admin on Sat Dec 16 15:39:56 GMT 2023 , Edited by admin on Sat Dec 16 15:39:56 GMT 2023
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MERCK INDEX
m3360
Created by admin on Sat Dec 16 15:39:56 GMT 2023 , Edited by admin on Sat Dec 16 15:39:56 GMT 2023
PRIMARY Merck Index
EVMPD
SUB06702MIG
Created by admin on Sat Dec 16 15:39:56 GMT 2023 , Edited by admin on Sat Dec 16 15:39:56 GMT 2023
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WIKIPEDIA
CHLORFENVINPHOS
Created by admin on Sat Dec 16 15:39:56 GMT 2023 , Edited by admin on Sat Dec 16 15:39:56 GMT 2023
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CAS
470-90-6
Created by admin on Sat Dec 16 15:39:56 GMT 2023 , Edited by admin on Sat Dec 16 15:39:56 GMT 2023
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FDA UNII
F2G9XS1W91
Created by admin on Sat Dec 16 15:39:56 GMT 2023 , Edited by admin on Sat Dec 16 15:39:56 GMT 2023
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NCI_THESAURUS
C80597
Created by admin on Sat Dec 16 15:39:56 GMT 2023 , Edited by admin on Sat Dec 16 15:39:56 GMT 2023
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SMS_ID
100000084312
Created by admin on Sat Dec 16 15:39:56 GMT 2023 , Edited by admin on Sat Dec 16 15:39:56 GMT 2023
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INN
2856
Created by admin on Sat Dec 16 15:39:56 GMT 2023 , Edited by admin on Sat Dec 16 15:39:56 GMT 2023
PRIMARY
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ACTIVE MOIETY
Definition References