Page last updated: 2024-11-05

dimethyldiselenide

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

Description

Dimethyl diselenide (DMDS) is an organoselenium compound with the formula (CH3)2Se2. It is a colorless liquid with a pungent odor. DMDS is a versatile reagent used in organic synthesis, and it is also a potential source of selenium in the diet. DMDS is synthesized by reacting methyl lithium with selenium. The synthesis of DMDS is important because it provides a starting point for the synthesis of other organoselenium compounds, which are used in a variety of applications, including pharmaceuticals, agrochemicals, and materials science. DMDS has been shown to have antioxidant and anti-inflammatory properties, and it may also have anticancer activity. However, DMDS is toxic and should be handled with care. Studies on DMDS focus on its role in the synthesis of other selenium compounds, its biological activity, and its potential environmental impact.'
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dimethyldiselenide: volatile selenium metabolite [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

dimethyl diselenide : An organoselenium compound that is diselane covalently bound to two methyl groups. It has been detected in onion-family vegetables and soft-necked garlics. It induces ER stress and toxic protein aggregation in the budding yeast, S. cerevisiae and used as a reagent to identify distonic radical cations. [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 CID23496
CHEBI ID176517
MeSH IDM0113336

Synonyms (28)

Synonym
1,2-dimethyldiselane
diselenide, dimethyl
CHEBI:176517
diselenobismethane
(methyldiselanyl)methane
dimethyldiselane
dimethyldiselenide
AKOS015840122
methyl diselenide
(ch3se)2
dimethyl diselenide, 96%
7101-31-7
dimethyl diselenide
D3290
A837049
ah7tj8228u ,
einecs 230-410-7
unii-ah7tj8228u
FT-0625133
DTXSID40221237
1,2-dimethyldiselane #
mfcd00008254
H10908
methyl diselenide, 8ci
AMY31938
SY048201
CS-0199215
diselane, 1,2-dimethyl-

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
" We investigated the metabolism of L-selenomethionine (SeMet) and selenite by probiotic bacteria in vitro and the disposition of selenium after probiotic treatment followed by oral dosing with SeMet and selenite in rats."( Metabolism of L-selenomethionine and selenite by probiotic bacteria: in vitro and in vivo studies.
Fawcett, JP; Krittaphol, W; McDowell, A; Tagg, JR; Thomson, CD; Wescombe, PA, 2011
)
0.37
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (4)

RoleDescription
bacterial metaboliteAny prokaryotic metabolite produced during a metabolic reaction in bacteria.
mammalian metaboliteAny animal metabolite produced during a metabolic reaction in mammals.
plant metaboliteAny eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
human xenobiotic metaboliteAny human metabolite produced by metabolism of a xenobiotic compound in humans.
[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 (1)

ClassDescription
organoselenium compoundAn organoselenium compound is a compound containing at least one carbon-selenium bond.
[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]

Pathways (2)

PathwayProteinsCompounds
superpathway of seleno-compound metabolism339
seleno-amino acid detoxification and volatilization III26
superpathway of seleno-compound metabolism744

Research

Studies (16)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (6.25)18.7374
1990's0 (0.00)18.2507
2000's8 (50.00)29.6817
2010's6 (37.50)24.3611
2020's1 (6.25)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 29.30

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 Index29.30 (24.57)
Research Supply Index2.94 (2.92)
Research Growth Index4.23 (4.65)
Search Engine Demand Index36.02 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (29.30)

All Compounds (24.57)

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%
Other18 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]