Page last updated: 2024-11-05

methylurea

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

Description

Methylurea is a white crystalline solid that is soluble in water and ethanol. It is synthesized by the reaction of methylamine with urea. Methylurea has been studied for its potential applications in various fields, including agriculture, medicine, and industry. For instance, it has been investigated as a fertilizer and as a herbicide, and it also shows promising activity against certain bacteria. Further research is ongoing to explore its full potential in various applications.'

N-methyl urea : A member of the class of ureas that is urea substituted by a methyl group at one of the nitrogen atoms. [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 CID11719
CHEBI ID44383
MeSH IDM0042898

Synonyms (51)

Synonym
methyl-urea
urea, methyl-
1-methylurea
monomethylurea
methylurea
598-50-5
urea, n-methyl-
n-methylurea
inchi=1/c2h6n2o/c1-4-2(3)5/h1h3,(h3,3,4,5
n-methylurea, 97%
methylharnstoff [german]
methyl urea
ccris 9137
methylmocovina [czech]
ai3-15088
einecs 209-935-0
STK400004
L000900
BMSE000738
M0455
AKOS000120665
A832503
BBL013131
ec 209-935-0
methylmocovina
vz89ybw3p8 ,
methylharnstoff
unii-vz89ybw3p8
FT-0628929
gtpl4662
DTXSID5060510
n-methyl urea
CHEBI:44383
3-methyl-urea
ch3nhconh2
56683-43-3
F0001-1568
mfcd00007950
n-methylurea, vetec(tm) reagent grade, 97%
1-methylurea;1-methylurea
methylisourea
J-505015
SY018863
Q5476523
STR01326
AMY40217
AC8061
methylurea-d6
EN300-17436
CS-W016687
Z56932989

Research Excerpts

Bioavailability

ExcerptReferenceRelevance
" The administration of an intragastric dose permitted the calculation of the systemic bioavailability of monomethylamine as 69 +/- 3%."( Deuterium isotope effect on the toxicokinetics of monomethylamine in the rat.
Heur, YH; Hrabie, JA; Keefer, LK; Mico, BA; Nims, RW; Ohannesian, L; Sheffels, PR; Streeter, AJ,
)
0.13
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
ureas
[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 (1)

PathwayProteinsCompounds
caffeine degradation V (bacteria, via trimethylurate)119

Research

Studies (41)

TimeframeStudies, This Drug (%)All Drugs %
pre-199021 (51.22)18.7374
1990's8 (19.51)18.2507
2000's7 (17.07)29.6817
2010's4 (9.76)24.3611
2020's1 (2.44)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 43.52

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

MetricThis Compound (vs All)
Research Demand Index43.52 (24.57)
Research Supply Index3.76 (2.92)
Research Growth Index4.35 (4.65)
Search Engine Demand Index63.16 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (43.52)

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%
Other42 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]