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
A concentration addition model to assess activation of the pregnane X receptor (PXR) by pesticide mixtures found in the French diet.
2014-09
Esterase metabolism of cholinesterase inhibitors using rat liver in vitro.
2011-03-15
Differential protein adduction by seven organophosphorus pesticides in both brain and thymus.
2007-04
Amphetamine- and scopolamine-induced locomotor activity following treatment with chlorphenvinphos or chlorphyriphos in rats.
2005
On the interactions between antimuscarinic atropine and NMDA receptor antagonists in anticholinesterase-treated mice.
2001-01
Reactivation by various oximes of human erythrocyte acetylcholinesterase inhibited by different organophosphorus compounds.
1996
Differences in the mode of lethality produced through intravenous and oral administration of organophosphorus insecticides in rats.
1991-04
Pretreatment of rats with an organophosphorus insecticide, chlorfenvinphos, protects against subsequent challenge with the same compound.
1990-04
Neurochemical alterations in rat brain as a test for studying the neurotoxicity of organophosphorus insecticides.
1980
Effects of insecticides in vitro and in vivo on esterase-6 in Drosophila melanogaster.
1978
Patents
Substance Class Mixture
Created
by admin
on Wed Apr 02 06:17:41 GMT 2025
Edited
by admin
on Wed Apr 02 06:17:41 GMT 2025
Record UNII
F2G9XS1W91
Record Status Validated (UNII)
Record Version
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Name Type Language
CLOFENVINFOS
INN   MART.  
INN  
Preferred Name English
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
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 Wed Apr 02 06:17:41 GMT 2025 , Edited by admin on Wed Apr 02 06:17:41 GMT 2025
Code System Code Type Description
ECHA (EC/EINECS)
207-432-0
Created by admin on Wed Apr 02 06:17:41 GMT 2025 , Edited by admin on Wed Apr 02 06:17:41 GMT 2025
PRIMARY
EPA CompTox
DTXSID7034250
Created by admin on Wed Apr 02 06:17:41 GMT 2025 , Edited by admin on Wed Apr 02 06:17:41 GMT 2025
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ALANWOOD
chlorfenvinphos
Created by admin on Wed Apr 02 06:17:41 GMT 2025 , Edited by admin on Wed Apr 02 06:17:41 GMT 2025
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MESH
D002709
Created by admin on Wed Apr 02 06:17:41 GMT 2025 , Edited by admin on Wed Apr 02 06:17:41 GMT 2025
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PUBCHEM
10107
Created by admin on Wed Apr 02 06:17:41 GMT 2025 , Edited by admin on Wed Apr 02 06:17:41 GMT 2025
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ChEMBL
CHEMBL2104653
Created by admin on Wed Apr 02 06:17:41 GMT 2025 , Edited by admin on Wed Apr 02 06:17:41 GMT 2025
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CHEBI
38598
Created by admin on Wed Apr 02 06:17:41 GMT 2025 , Edited by admin on Wed Apr 02 06:17:41 GMT 2025
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HSDB
1540
Created by admin on Wed Apr 02 06:17:41 GMT 2025 , Edited by admin on Wed Apr 02 06:17:41 GMT 2025
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MERCK INDEX
m3360
Created by admin on Wed Apr 02 06:17:41 GMT 2025 , Edited by admin on Wed Apr 02 06:17:41 GMT 2025
PRIMARY Merck Index
EVMPD
SUB06702MIG
Created by admin on Wed Apr 02 06:17:41 GMT 2025 , Edited by admin on Wed Apr 02 06:17:41 GMT 2025
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WIKIPEDIA
CHLORFENVINPHOS
Created by admin on Wed Apr 02 06:17:41 GMT 2025 , Edited by admin on Wed Apr 02 06:17:41 GMT 2025
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CAS
470-90-6
Created by admin on Wed Apr 02 06:17:41 GMT 2025 , Edited by admin on Wed Apr 02 06:17:41 GMT 2025
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FDA UNII
F2G9XS1W91
Created by admin on Wed Apr 02 06:17:41 GMT 2025 , Edited by admin on Wed Apr 02 06:17:41 GMT 2025
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NCI_THESAURUS
C80597
Created by admin on Wed Apr 02 06:17:41 GMT 2025 , Edited by admin on Wed Apr 02 06:17:41 GMT 2025
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SMS_ID
100000084312
Created by admin on Wed Apr 02 06:17:41 GMT 2025 , Edited by admin on Wed Apr 02 06:17:41 GMT 2025
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INN
2856
Created by admin on Wed Apr 02 06:17:41 GMT 2025 , Edited by admin on Wed Apr 02 06:17:41 GMT 2025
PRIMARY
All of the following components must be present:
Related Record Type Details
ACTIVE MOIETY
Definition References