Page last updated: 2024-09-22

methiocarb sulfoxide

Description

methiocarb sulfoxide: a metabolite of methiocarb; structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

methiocarb-sulfoxide : A carbamate ester obtained by the formal condensation of the phenolic group of 3,5-dimethyl-4-(methylsulfinyl)phenol with the carboxy group of methylcarbamic acid. It is a metabolite of the pesticide methiocarb. [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]

Cross-References

ID SourceID
PubMed CID17521
CHEBI ID83542
SCHEMBL ID5934106
MeSH IDM0257283

Synonyms (36)

Synonym
phenol, 3,5-dimethyl-4-(methylsulfinyl)-, methylcarbamate
methiocarb sulfoxide
3,5-dimethyl-4-(methylsulfinyl)phenyl methylcarbamate
carbamic acid, methyl-, 4-(methylsulfinyl)-3,5-xylyl ester
brn 2130137
mesurol sulfoxide
bay 37344 sulfoxide
carbamic acid, methyl-, 3,5-dimethyl-4-(methylsulfinyl)phenyl ester
bay 41791
ent 25824
bayer 41791
ai3-25824
(3,5-dimethyl-4-methylsulfinylphenyl) n-methylcarbamate
s9303l7a4d ,
unii-s9303l7a4d
2635-10-1
SCHEMBL5934106
methiocarb-sulfoxide
CHEBI:83542
4-(methylsulfinyl)-3,5-xylyl methylcarbamate
FNCMBMZOZQAWJA-UHFFFAOYSA-N
phenol, 3,5-dimethyl-4-(methylsulfinyl)-, (n-methylcarbamate)
bay-37344 sulfoxide
bay-41791
phenol, 3,5-dimethyl-4-(methylsulfinyl)-, 1-(n-methylcarbamate)
methiocarb sulphoxide
DTXSID8042139
methiocarb sulfoxide, pestanal(r), analytical standard
J-016392
4-methanesulfinyl-3,5-dimethylphenyl n-methylcarbamate
methiocarb sulphoxide (m01)
methiocarb tp1
Q27156936
methiocarb-sulfoxide 100 microg/ml in acetonitrile
CAA63510
1ST20265

Roles (1)

RoleDescription
marine xenobiotic metaboliteAny metabolite produced by metabolism of a xenobiotic compound in marine macro- and microorganisms.
[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
sulfoxideAn organosulfur compound having the structure R2S=O or R2C=S=O (R =/= H).
carbamate esterAny ester of carbamic acid or its N-substituted derivatives.
[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]

Research

Studies (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's1 (20.00)18.2507
2000's0 (0.00)29.6817
2010's4 (80.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research Highlights

Interactions (1)

ArticleYear
In Vitro Drug-Drug Interaction Potential of Sulfoxide and/or Sulfone Metabolites of Albendazole, Triclabendazole , Aldicarb, Methiocarb, Montelukast and Ziprasidone.
Drug metabolism letters, Volume: 12, Issue: 2
2018
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]