Page last updated: 2024-12-05

formothion

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

Description

formothion: was MH 1976-91 (see under INSECTICIDES, ORGANOTHIOPHOSPHATE 1976-90) [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID17345
CHEMBL ID449733
CHEBI ID82126
SCHEMBL ID116325
MeSH IDM0185259

Synonyms (81)

Synonym
phosphorodithioic acid, s-[2-(formylmethylamino)-2-oxoethyl] o,o-dimethyl ester
formothion
einecs 219-818-6
toprose
oms-968
o,o-dimethyl phosphorodithioate s-ester with n-formyl-2-mercapto-n-methylacetamide
2-dimethoxyphosphinothioylthio-n-formyl-n-methylacetamide
o,o-dimetil-s-(n-formil-n-metil-carbamoil-metil)-ditiofosfato [italian]
vel 4284
s-(2-(formylmethylamino)-2-oxoethyl) o,o-dimethylphosphorodithioate
o,o-dimethyl s-(n-formyl-n-methylcarbamoylmethyl) phosphorodithioate
phosphorodithioic acid, o,o-dimethyl ester, s-ester with n-formyl-2-mercapto-n-methyl-acetamide
anthio 25
j-38
s-(n-formyl-n-methylcarbamoylmethyl) dimethyl phosphorothiolothionate
san 6913 i
san 7107 i
phosphorodithioic acid, o,o-dimethyl ester, n-formyl-2-mercapto-n-methylacetamide s-ester
phosphorodithioic acid s-(2-(formylmethylamino)-2-oxoethyl) o,o-dimethyl ester
ccris 5213
formothion 25 ec
sandoz s-6900
ai3-27257
san 244 i
o,o-dimethyl phosphorodithioate n-formyl-2-mercapto-n-methylacetamide s-ester
hsdb 1587
s-(formyl(methyl)carbamoylmethyl) o,o-dimethyl phosphorodithioate
o,o-dimethyl dithiophosphorylacetic acid n-methyl-n-formylamide
brn 5942199
aflix
anthio
spencer s-6900
s 6900
ent 27,257
caswell no. 366c
acetamide, n-formyl-2-mercapto-n-methyl-, s-ester with o,o-dimethyl phosphorodithioate
cp 53926
o,o-dimethyl-s-(n-methyl-n-formyl-carbamoylmethyl)-dithiophosphat [german]
phosphorodithioic acid, s-(2-(formylmethylamino)-2-oxoethyl) o,o-dimethyl ester
o,o-dimethyl s-(n-methyl-n-formylcarbamoylmethyl)phosphorodithioate
s-(2-(formylmethylamino)-2-oxoethyl) o,o-dimethyl phosphorodithioate
formothion [bsi:iso]
epa pesticide chemical code 366400
s-(n-formyl-n-methylcarbamoylmethyl) o,o-dimethyl phosphorodithioate
o,o-dimethyl-s-(3-methyl-2,4-dioxo-3-aza-butyl)-dithiophosphat [german]
antio
n-formyl-n-methylcarbamoylmethyl o,o-dimethyl phosphorodithioate
afliz [sandoz]
o,o-dimethyl-s-(3-methyl-2,4-dioxo-3-aza-butyl)-dithiofosfaat [dutch]
2-dimethoxyphosphinothioylsulfanyl-n-formyl-n-methylacetamide
CHEMBL449733
chebi:82126 ,
2540-82-1
C18988
o,o-dimetil-s-(n-formil-n-metil-carbamoil-metil)-ditiofosfato
o,o-dimethyl-s-(n-methyl-n-formyl-carbamoylmethyl)-dithiophosphat
o,o-dimethyl-s-(3-methyl-2,4-dioxo-3-aza-butyl)-dithiophosphat
o,o-dimethyl-s-(3-methyl-2,4-dioxo-3-aza-butyl)-dithiofosfaat
unii-7o9ewv477r
afliz
7o9ewv477r ,
s-[2-(formylmethylamino)-2-oxoethyl] o,o-dimethyl dithiophosphate
AKOS015898765
formothion [hsdb]
formothion [mi]
phosphorodithioic acid o,o-dimethyl ester s-ester with n-formyl-2-mercapto-n-methylacetamide
formothion [iso]
SCHEMBL116325
o,o-dimethyl-s-(3-methyl-2,4-dioxo-3-azabutyl)dithiofosfaat
o,o-dimethyl-s-(n-methyl-n-formylcarbamoylmethyl)dithiophosphat
o,o-dimetil-s-(n-formil-n-metilcarbamoilmetil)ditiofosfato
s-(2-[formyl(methyl)amino]-2-oxoethyl) o,o-dimethyl dithiophosphate #
phosphorodithioic acid, o,o-dimethyl ester, s-ester with n-formyl-2-mercapto-n-methylacetamide
o,o-dimethyl-s-(3-methyl-2,4-dioxo-3-azabutyl)dithiophosphat
DTXSID4041991
formothion 100 microg/ml in acetonitrile
J-015984
Q5470249
anthio 25;ent 27257;cp 53926
j 38
CAA54082
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
dicarboximideAn imide in which the two acyl substituents on nitrogen are carboacyl groups.
[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]

Bioassays (2)

Assay IDTitleYearJournalArticle
AID399287In vivo inhibition of acetylcholinesterase from nerve tissue of Lymnaea acuminata at 27 mg/L relative to control
AID399291Inhibition of acetylcholinesterase from nerve tissue of Lymnaea acuminata at 0.75 ug w/v relative to control
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (12)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (8.33)18.7374
1990's8 (66.67)18.2507
2000's1 (8.33)29.6817
2010's1 (8.33)24.3611
2020's1 (8.33)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 28.27

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 Index28.27 (24.57)
Research Supply Index2.71 (2.92)
Research Growth Index5.29 (4.65)
Search Engine Demand Index27.81 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (28.27)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies1 (7.14%)4.05%
Observational0 (0.00%)0.25%
Other13 (92.86%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]