Page last updated: 2024-11-05

monosulfiram

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

Description

monosulfiram: monosulfide derivative of disulfide DISULFIRAM; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID7215
CHEMBL ID2004297
CHEBI ID135093
SCHEMBL ID160769
MeSH IDM0054875

Synonyms (65)

Synonym
ttms
monosulfiram
methanethioamide,1'-thiobis[n,n-diethyl-
nsc36731
formamide,1'-thiobis(n,n'-diethylthio-
bis(diethylthiocarbamyl) sulfide
sulfiramum
sarcocide b
kutka
sulfiram
formamide,1'-thiobis[n,n-diethylthio-
95-05-6
sulfide, bis[(diethylamino)thioxomethyl]
tetraethylthiuram monosulfide
carbamic anhydride, tetraethyltrithio-
thiodicarbonic diamide ([(h2n)c(s)]2s), tetraethyl-
wln: 2n2&yus&syus&n2&2
tetmos
sanigal
sulfirame
tetrucid
tetmosol
nsc-36731
thiuram monosulfide, tetraethyl-
sulfide, bis(diethylthiocarbamoyl)
bis(n,n-diethylthiocarbamoyl) sulfide
tetraethyl thiuram monosulfide
NCI60_003379
formamide, 1,1'-thiobis(n,n'-diethylthio-
carbamodithioic acid, diethyl-, anhydrosulfide
einecs 202-387-3
sulfiram [inn]
sulfide, bis((diethylamino)thioxomethyl)
methanethioamide, 1,1'-thiobis(n,n-diethyl-
brn 1789060
tetraethylthiuram-monosulfid
thiodicarbonic diamide (((h2n)c(s))2s), tetraethyl-
thiodicarbonic diamide, tetraethyl-
nsc 36731
ai3-00996
sulfiramum [inn-latin]
carbamic acid, diethyldithio-, anhydrosulfide
CHEBI:135093
diethylcarbamothioyl n,n-diethylcarbamodithioate
sulfiram (inn)
tetmosol (tn)
D08545
CHEMBL2004297
FT-0674772
unii-1xhl4q8p7y
4-04-00-00397 (beilstein handbook reference)
1xhl4q8p7y ,
sulfiram [inn:ban]
SCHEMBL160769
sulfiram [who-dd]
tetraethylthiodicarbonic diamide ((((c(sub 2)h(sub 5))(sub 2)n)c(s))(sub 2)s)
sulfiram [mart.]
sulfiram [mi]
DTXSID5058222
n,n-diethyl[(diethylcarbamothioyl)sulfanyl]carbothioamide
Q7636201
CS-0083488
HY-121817
bdbm50555840
AKOS040742657
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
organosulfur compoundAn organosulfur compound is a compound containing at least one carbon-sulfur 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]

Protein Targets (1)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Fructose-1,6-bisphosphatase 1Homo sapiens (human)IC50 (µMol)10.00000.01002.00979.8000AID1703767
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (20)

Processvia Protein(s)Taxonomy
negative regulation of transcription by RNA polymerase IIFructose-1,6-bisphosphatase 1Homo sapiens (human)
fructose 6-phosphate metabolic processFructose-1,6-bisphosphatase 1Homo sapiens (human)
gluconeogenesisFructose-1,6-bisphosphatase 1Homo sapiens (human)
regulation of gluconeogenesisFructose-1,6-bisphosphatase 1Homo sapiens (human)
dephosphorylationFructose-1,6-bisphosphatase 1Homo sapiens (human)
negative regulation of cell growthFructose-1,6-bisphosphatase 1Homo sapiens (human)
response to nutrient levelsFructose-1,6-bisphosphatase 1Homo sapiens (human)
cellular response to insulin stimulusFructose-1,6-bisphosphatase 1Homo sapiens (human)
negative regulation of glycolytic processFructose-1,6-bisphosphatase 1Homo sapiens (human)
negative regulation of Ras protein signal transductionFructose-1,6-bisphosphatase 1Homo sapiens (human)
cellular response to magnesium ionFructose-1,6-bisphosphatase 1Homo sapiens (human)
cellular response to cAMPFructose-1,6-bisphosphatase 1Homo sapiens (human)
cellular response to xenobiotic stimulusFructose-1,6-bisphosphatase 1Homo sapiens (human)
cellular hyperosmotic salinity responseFructose-1,6-bisphosphatase 1Homo sapiens (human)
cellular hypotonic salinity responseFructose-1,6-bisphosphatase 1Homo sapiens (human)
cellular response to raffinoseFructose-1,6-bisphosphatase 1Homo sapiens (human)
cellular response to phorbol 13-acetate 12-myristateFructose-1,6-bisphosphatase 1Homo sapiens (human)
fructose 1,6-bisphosphate metabolic processFructose-1,6-bisphosphatase 1Homo sapiens (human)
fructose metabolic processFructose-1,6-bisphosphatase 1Homo sapiens (human)
sucrose biosynthetic processFructose-1,6-bisphosphatase 1Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (7)

Processvia Protein(s)Taxonomy
protein bindingFructose-1,6-bisphosphatase 1Homo sapiens (human)
AMP bindingFructose-1,6-bisphosphatase 1Homo sapiens (human)
fructose 1,6-bisphosphate 1-phosphatase activityFructose-1,6-bisphosphatase 1Homo sapiens (human)
identical protein bindingFructose-1,6-bisphosphatase 1Homo sapiens (human)
metal ion bindingFructose-1,6-bisphosphatase 1Homo sapiens (human)
monosaccharide bindingFructose-1,6-bisphosphatase 1Homo sapiens (human)
RNA polymerase II-specific DNA-binding transcription factor bindingFructose-1,6-bisphosphatase 1Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (4)

Processvia Protein(s)Taxonomy
nucleusFructose-1,6-bisphosphatase 1Homo sapiens (human)
cytoplasmFructose-1,6-bisphosphatase 1Homo sapiens (human)
cytosolFructose-1,6-bisphosphatase 1Homo sapiens (human)
extracellular exosomeFructose-1,6-bisphosphatase 1Homo sapiens (human)
cytoplasmFructose-1,6-bisphosphatase 1Homo sapiens (human)
cytosolFructose-1,6-bisphosphatase 1Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (2)

Assay IDTitleYearJournalArticle
AID1703825Inhibition of wild-type full-length human liver FBPase expressed in Escherichia coli BL21 (DE3) using FBP as substrate at 10 uM by malachite green dye-based assay2020European journal of medicinal chemistry, Oct-01, Volume: 203Development of disulfide-derived fructose-1,6-bisphosphatase (FBPase) covalent inhibitors for the treatment of type 2 diabetes.
AID1703767Inhibition of wild-type full-length human liver FBPase expressed in Escherichia coli BL21 (DE3) using FBP as substrate by malachite green dye based assay2020European journal of medicinal chemistry, Oct-01, Volume: 203Development of disulfide-derived fructose-1,6-bisphosphatase (FBPase) covalent inhibitors for the treatment of type 2 diabetes.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (16)

TimeframeStudies, This Drug (%)All Drugs %
pre-19905 (31.25)18.7374
1990's7 (43.75)18.2507
2000's2 (12.50)29.6817
2010's1 (6.25)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: 52.73

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 very strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index52.73 (24.57)
Research Supply Index2.89 (2.92)
Research Growth Index4.45 (4.65)
Search Engine Demand Index97.96 (26.88)
Search Engine Supply Index2.46 (0.95)

This Compound (52.73)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (6.25%)5.53%
Reviews1 (6.25%)6.00%
Case Studies1 (6.25%)4.05%
Observational0 (0.00%)0.25%
Other13 (81.25%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]