Page last updated: 2024-12-05

fonofos

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

Description

Fonofos: An organothiophosphorus cholinesterase inhibitor that is used as an insecticide. [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID13676
CHEMBL ID3187845
CHEBI ID38689
SCHEMBL ID74085
MeSH IDM0006906

Synonyms (61)

Synonym
unii-p4vt8081qo
o-aethyl-s-phenyl-aethyl-dithiophosphonat
p4vt8081qo ,
o-ethyl s-phenyl ethylphosphonrothiolothionate
fonofos
(+-)-fonofos
brn 1958949
stauffer n2790
ai3-25796
difonate
fonophos
difonatul
dyfonate
n-2790 ,
doubledown
phosphonodithioic acid, ethyl-, o-ethyl s-phenyl ester
caswell no. 454b
stauffer n 2790
n-2788 ,
fonofos [iso]
epa pesticide chemical code 041701
dyfonate tillam 1-4e
einecs 213-408-0
oms 410
hsdb 1717
ent 25,796
o-ethyl s-phenyl ethyldithiophosphonate
o-aethyl-s-phenyl-aethyl-dithiophosphonat [german]
o-ethyl s-phenyl ethylphosphonothiolothionate
o-ethyl-s-phenyl ethylphosphonodithioate
CHEBI:38689 ,
(+-)-o-ethyl s-phenyl ethylphosphonodithioate
ethylphosphonodithioic acid o-ethyl s-phenyl ester
dyphonate
o-ethyl s-phenyl ethylphosphonodithioate
944-22-9
NCGC00248489-01
C18987
dtxsid2024113 ,
NCGC00257563-01
tox21_200009
dtxcid104113
cas-944-22-9
AKOS015902803
SCHEMBL74085
(rs)-(o-ethyl s-phenyl ethylphosphonodithioate)
o-ethyl s-phenyl p-ethylphosphonodithioate
dyphonate [hsdb]
fonofos [mi]
994-22-9
n 2790
dyfonate 10g
(.+/-.)-o-ethyl s-phenyl ethylphosphonodithioate
dyfonat
CHEMBL3187845
fonofos, analytical standard
fonofos 10 microg/ml in cyclohexane
fonofos 100 microg/ml in acetonitrile
Q2080990
ethoxy-ethyl-phenylsulfanyl-sulfanylidene-lambda5-phosphane
fonofos 1000 microg/ml in methanol

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
" Based on dosage mortality curves obtained with increasing amounts of atrazine, mortalities of 50 percent of the insect populations would have been achieved with 23, 40, 6, and 10 micrograms of atrazine added to the abovementioned dosages of carbofuran, DDT, parathion, and diazinon, respectively."( Synergism of insecticides by herbicides.
Anderegg, BN; Liang, TT; Lichtenstein, EP, 1973
)
0.25
[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.
EC 3.1.1.8 (cholinesterase) inhibitorAn EC 3.1.1.* (carboxylic ester hydrolase) inhibitor that interferes with the action of cholinesterase (EC 3.1.1.8).
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 (2)

ClassDescription
organic thiophosphate
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 (5)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
acetylcholinesteraseHomo sapiens (human)Potency32.61910.002541.796015,848.9004AID1347395; AID1347399
AR proteinHomo sapiens (human)Potency31.24770.000221.22318,912.5098AID1259243; AID1259247
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency27.19500.001022.650876.6163AID1224839
cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_aHomo sapiens (human)Potency27.19500.001723.839378.1014AID743083
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency72.35840.000323.4451159.6830AID743067
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (38)

TimeframeStudies, This Drug (%)All Drugs %
pre-199018 (47.37)18.7374
1990's7 (18.42)18.2507
2000's7 (18.42)29.6817
2010's4 (10.53)24.3611
2020's2 (5.26)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 32.46

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 moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index32.46 (24.57)
Research Supply Index3.83 (2.92)
Research Growth Index4.47 (4.65)
Search Engine Demand Index40.31 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (32.46)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies1 (2.22%)4.05%
Observational0 (0.00%)0.25%
Other44 (97.78%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]