Page last updated: 2024-11-05

phenylphosphonothioic acid, 2-ethyl 2-(4-nitrophenyl) ester

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

Phenylphosphonothioic Acid, 2-Ethyl 2-(4-Nitrophenyl) Ester: An organothiophosphorus cholinesterase inhibitor that is used as an insecticide and as a acaricide. [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID16421
CHEMBL ID3184641
CHEBI ID34733
SCHEMBL ID2124407
MeSH IDM0007607

Synonyms (118)

Synonym
phosphonothioic acid, phenyl-, o-ethyl o-(4-nitrophenyl) ester
phosphonothioic acid, phenyl-, o-ethyl o-(p-nitrophenyl) ester
o-ethyl o-(p-nitrophenyl phenyl)phosphonothioate
nsc8943
nsc-8943
o-ethyl o-(4-nitrophenyl)phenylphosphonothioate
ethyl p-nitrophenyl benzenethionophosphonate
CHEBI:34733 ,
o-ethyl o-p-nitrophenyl phenylphosphonothioate
o-ethyl phenylphosphonothioic acid o-(4-nitrophenyl) ester
phenylphosphonothioic acid o-ethyl o-(4-nitrophenyl) ester
ai3-17798
ethyl p-nitrophenyl benzenethiophosphate
o-ethyl o-p-nitrophenyl phenylphosphorothioate
o-etil-o-((4-nitro-fenil)-fenil)-monotiofosfonato [italian]
o-ethyl phenyl p-nitrophenyl thiophosphonate
ethyl p-nitrophenylthiobenzene phosphonate
ethyl p-nitrophenyl phenylphosphonothioate
ethyl (p-nitrophenyl)thionobenzenephosphonate
o-ethyl o-(p-nitrophenyl) phenylphosphonothionate
ethyl p-nitrophenyl thionobenzenephosphate
o-ethyl o-p-nitrophenyl phenylphosphonothiolate
oms 219
nsc 404840
o-aethyl-o-(4-nitro-phenyl)-phenyl-monothiophosphonat [german]
phenol, p-nitro-, o-ester with o-ethyl phenyl phosphonothioate
kasutop dust
benzenephosphothionic acid, ethyl-4-nitrophenyl ester
ethyl-p-nitrophenylthionobenzenephosphate
epa pesticide chemical code 041801
phenylphosphonothioic acid o-ethyl o-p-nitrophenyl ester
o-ethyl-o-p-nitrofenylester kyseliny fenylthiofosfonove [czech]
ethyl p-nitrophenyl benzenethiophosphonate
tsumaphos
nsc 8943
meidon 15 dust
o-ethyl-o-((4-nitro-fenyl)-fenyl)-monothiofosfonaat [dutch]
brn 2542580
phenylphosphonothioic acid, 2-ethyl 2-(4-nitrophenyl) ester
benzenephosphonic acid, thiono-, ethyl-p-nitrophenyl ester
phenylthiophosphonate de o-ethyle et o-4-nitrophenyle [french]
o-(4-nitrophenyl) o-ethyl phenyl thiophosphonate
hsdb 4049
ethoxy-4-nitrophenoxyphenylphosphine sulfide
caswell no. 454
o-ethyl-o-p-nitrophenylphenylphosphonothioate
o-ethyl o-4-nitrophenyl phenylphosphonothioate
ethyl p-nitrophenyl thionobenzenephosphonate
einecs 218-276-8
mapj
o-ethyl o-(4-nitrophenyl)benzenethionophosphonate
phenylphosphonothioate, o-ethyl-o-p-nitrophenyl-
wln: wnr dops&r&o2
nsc404840
phenylthiophosphonate de o-ethyle et o-4-nitrophenyle
ethyl (p-nitrophenyl) thionobenzenephosphonate
o-etil-o-((4-ntiro-fenil)-fenil)-monotiofosfonato
ethyl (p-nitrophenyl) benzenethiophosphate
o-aethyl-o-(4-nitro-phenyl)-phenyl-monothiophosphonat
ethyl (p-nitrophenyl) thionobenzenephosphate
phenol, o-ester with o-ethyl phenyl phosphonothioate
o-ethyl o-(4-nitrophenyl) benzenethionophosphonate
ethoxy-[[(4-nitrophenoxy)phenyl]phosphine] sulfide
nsc-404840
o-ethyl o-(4-nitrophenyl) phenylphosphonothioate
epn 300
o-ethyl o-(p-nitrophenyl) phenylphosphonothioate
o-ethyl o-(p-nitrophenyl) phenylphosphonothiolate
PIN ,
ethyl (p-nitrophenyl) benzenethionophosphonate
phosphonothioic acid, o-ethyl o-(p-nitrophenyl) ester
2104-64-5
o-ethyl o-(p-nitrophenyl) phenylphosphorothioate
benzenephosphonic acid, ethyl-(p-nitrophenyl) ester
phosphonothioic acid, o-ethyl o-(4-nitrophenyl) ester
EPN ,
o-ethyl phenyl (p-nitrophenyl) thiophosphonate
ethyl (p-nitrophenyl) benzenethiophosphonate
santox
phenylphosphonothioic acid, o-ethyl o-(4-nitrophenyl) ester
ethyl (p-nitrophenyl) phenylphosphonothioate
ent 17,798
phosphonothioic acid, o-ethyl o-(p-nitrophenyl)ester
o-ethyl o-(p-nitrophenyl) benzenethiophosphonate
o-ethyl-o-((4-nitro-fenyl)-fenyl)-monothiofosfonaat
ethyl p-nitrophenyl phenylphosphorothioate
phosphonothioic acid, phenyl-, o-ethyl o- (p-nitrophenyl) ester
NCGC00248026-01
9y6hp0hya8 ,
o-etil-o-((4-nitro-fenil)-fenil)-monotiofosfonato
unii-9y6hp0hya8
o-ethyl-o-p-nitrofenylester kyseliny fenylthiofosfonove
tox21_300424
cas-2104-64-5
NCGC00254507-01
dtxsid7022174 ,
dtxcid102174
SCHEMBL2124407
AKOS015888311
o-ethyl o-p-nitrophenyl benzenethiophosphonate
epn [mi]
epn [hsdb]
phosphonothioic acid, phenyl-, o-ethyl o- (4-nitrophenyl) ester
AIGRXSNSLVJMEA-UHFFFAOYSA-N
ethoxy-(((4-nitrophenoxy)phenyl)phosphine) sulfide
benzenephosphonic acid, thiono-, ethyl-(p-nitrophenyl) ester
CHEMBL3184641
epn, 100 mug/ml in acetonitrile, pestanal(r), analytical standard
epn, pestanal(r), analytical standard
epn 100 microg/ml in acetonitrile
epn 10 microg/ml in cyclohexane
epn 100 microg/ml in cyclohexane
ethoxy-(4-nitrophenoxy)-phenyl-sulfanylidene-lambda^{5}-phosphane
J-013797
Q2007270
phosphonothioic acid, p-phenyl-, o-ethyl o-(4-nitrophenyl) ester
o-ethyl o-(4-nitrophenyl)benzenethiophosphonate
CAA10464

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" It is believed that the phosphonate ester configuration of EPN and Leptophos has a specific mode of toxic action which is mainly located at the central nervous system."( Neurotoxicity of organophosphorus insecticides Leptophos and EPN.
Ahmed, NS; El-Sebae, AH; Elamayem, MA; Soliman, SA, 1977
)
0.26
"The oral LD50 of a compound in hens does not reliably predict the neurotoxic dose of that compound."( Consideration of dose levels for delayed neurotoxicity testing in hens: the relationship of neurotoxic dosages to acute LD50 values.
Hixson, EJ, 1983
)
0.27
" A significant difference was found between the enantiomers in their acute aquatic toxicity; the (+)-enantiomer was about 10 times more toxic than its antipode."( Separation and aquatic toxicity of enantiomers of the organophosphorus insecticide O-ethyl O-4-nitrophenyl phenylphosphonothioate (EPN).
Liu, J; Sun, J; Tu, W; Xu, C, 2010
)
0.36

Compound-Compound Interactions

ExcerptReferenceRelevance
"This investigation was designed to study the neurotoxicity produced in hens by the aliphatic hexacarbons n-hexane, methyl n-butyl ketone (MnBK), 2,5-hexanediol (2,5-HDOH), and 2,5-hexanedione (2,5-HD) following daily dermal application of each chemical alone and in combination with O-ethyl O-4-nitrophenyl phenylphosphonothioate (EPN)."( Pattern of neurotoxicity of n-hexane, methyl n-butyl ketone, 2,5-hexanediol, and 2,5-hexanedione alone and in combination with O-ethyl O-4-nitrophenyl phenylphosphonothioate in hens.
Abou-Donia, MB; Campbell, GM; Makkawy, HM, 1985
)
0.27

Dosage Studied

ExcerptRelevanceReference
" The oral LD50 in rats does not predict either the oral LD50 in hens or the neurotoxic dose in hens, so there is no justification for using the rat value to predict the neurotoxic dosage in hens."( Consideration of dose levels for delayed neurotoxicity testing in hens: the relationship of neurotoxic dosages to acute LD50 values.
Hixson, EJ, 1983
)
0.27
" On the other hand, none of the EPN-treated sheep showed clinical signs of neurotoxicity during the course of the experiment at the dosage tested."( Six-month daily treatment of sheep with neurotoxic organophosphorus compounds.
Curley, A; Durham, WF; Farmer, JD; Soliman, SA; Svendsgaard, D, 1983
)
0.27
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
EC 3.1.1.7 (acetylcholinesterase) inhibitorAn EC 3.1.1.* (carboxylic ester hydrolase) inhibitor that interferes with the action of enzyme acetylcholinesterase (EC 3.1.1.7), which helps breaking down of acetylcholine into choline and acetic acid.
acaricideA substance used to destroy pests of the subclass Acari (mites and ticks).
agrochemicalAn agrochemical is a substance that is used in agriculture or horticulture.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (3)

ClassDescription
organic phosphonate
phosphonic esterA phosphonic acid derivative in which one or both OH groups have been esterified.
organothiophosphate insecticide
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Protein Targets (10)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
acetylcholinesteraseHomo sapiens (human)Potency2.00050.002541.796015,848.9004AID1347399
GLI family zinc finger 3Homo sapiens (human)Potency13.68540.000714.592883.7951AID1259392
AR proteinHomo sapiens (human)Potency11.68700.000221.22318,912.5098AID1259243; AID1259247
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency10.91880.001022.650876.6163AID1224838; AID1224839; AID1224893
progesterone receptorHomo sapiens (human)Potency2.16900.000417.946075.1148AID1346795
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency0.00150.001530.607315,848.9004AID1224849
estrogen nuclear receptor alphaHomo sapiens (human)Potency27.30600.000229.305416,493.5996AID743079
peroxisome proliferator activated receptor gammaHomo sapiens (human)Potency24.54120.001019.414170.9645AID743094
aryl hydrocarbon receptorHomo sapiens (human)Potency37.40800.000723.06741,258.9301AID743085; AID743122
thyroid stimulating hormone receptorHomo sapiens (human)Potency24.33650.001628.015177.1139AID1224895
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (81)

TimeframeStudies, This Drug (%)All Drugs %
pre-199064 (79.01)18.7374
1990's5 (6.17)18.2507
2000's7 (8.64)29.6817
2010's4 (4.94)24.3611
2020's1 (1.23)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 9.88

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index9.88 (24.57)
Research Supply Index4.45 (2.92)
Research Growth Index4.33 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (9.88)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (1.18%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other84 (98.82%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]