Page last updated: 2024-11-05

1,1-dimethylurea

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

1,1-Dimethylurea, also known as dimethylurea (DMU) and sym-dimethylurea, is a colorless crystalline solid. It is a derivative of urea, with two methyl groups attached to the nitrogen atom. DMU is an important intermediate in the synthesis of pesticides, herbicides, and pharmaceuticals. It is also used as a fertilizer and a feed supplement. DMU is produced by the reaction of urea with methanol in the presence of a catalyst. DMU is a potent inhibitor of urease, an enzyme that breaks down urea. This property makes it a useful herbicide, as it can inhibit the growth of plants that rely on urease to obtain nitrogen. DMU is also a known teratogen, meaning that it can cause birth defects. It is therefore important to handle DMU with care and to avoid exposure to it during pregnancy. DMU is being studied for its potential to treat cancer, as it has been shown to inhibit the growth of certain types of cancer cells. DMU is also being investigated for its potential to be used as a biofuel.'

Cross-References

ID SourceID
PubMed CID11737
MeSH IDM0069624

Synonyms (45)

Synonym
1320-50-9
EN300-17007
1,1-dimethyl-urea
urea, 1,1-dimethyl-
1,1-dimethylurea
nsc33603
nsc-33603
598-94-7
asym-dimethylurea
n,n-dimethylurea
inchi=1/c3h8n2o/c1-5(2)3(4)6/h1-2h3,(h2,4,6
1.1-dimethylurea
urea, n,n-dimethyl-
1,1-dimethylurea, 99%
n,n-dimethylharnstoff [german]
ai3-61297
einecs 209-957-0
nsc 33603
hsdb 4273
brn 1740666
D-5580
D0809
AKOS000200400
A832531
einecs 215-303-5
unii-i988r763p3
i988r763p3 ,
n,n-dimethylharnstoff
FT-0606140
1,1-dimethylurea [hsdb]
dimethylurea, n,n-
n,n-dimethyl urea
DTXSID0060515
STR03134
(ch3)2nconh2
mfcd00007959
STL482999
CS-0132397
1,1-dimethyl urea
Q24712449
BB 0311004
1,1-dimethyl-d6-urea
1219802-32-0
D89723
SY048169

Research Excerpts

Toxicity

ExcerptReferenceRelevance
"Dimethylthiourea (DMTU) is a small, highly diffusible molecule that effectively scavenges toxic oxygen metabolites in vitro and reduces oxidative injury in many biologic systems."( Toxic effects of dimethylthiourea in rats.
Beehler, CJ; Ely, ME; Reiss, OK; Repine, JE; Rutledge, KS; Shanley, PF; Simchuk, ML, 1994
)
0.29
"Subcutaneous administration of the LD50 dose of methyl isocyanate (MIC) to rats induced severe hyperglycaemia, lactic acidosis and uraemia in rats."( Influence of methylamine and N,N'-dimethylurea, the hydrolysis products of methyl isocyanate, on its systemic toxicity.
Jeevaratnam, K; Sugendran, K; Vaidyanathan, CS,
)
0.13
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (33)

TimeframeStudies, This Drug (%)All Drugs %
pre-199014 (42.42)18.7374
1990's12 (36.36)18.2507
2000's2 (6.06)29.6817
2010's5 (15.15)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 30.37

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 Index30.37 (24.57)
Research Supply Index3.56 (2.92)
Research Growth Index4.44 (4.65)
Search Engine Demand Index30.68 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (30.37)

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%
Other34 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]