Page last updated: 2024-12-05

3-buten-2-one

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

Description

3-Buten-2-one, also known as methyl vinyl ketone (MVK), is a highly reactive α,β-unsaturated ketone. It is a colorless liquid with a pungent odor. MVK is commonly synthesized through the aldol condensation of acetone and formaldehyde. It is an important intermediate in organic synthesis, finding use in the production of various chemicals and polymers. MVK is also a key component of many natural products and fragrances. Due to its reactivity, it is used as a building block in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Research into 3-buten-2-one focuses on its applications in organic synthesis, its role in biological processes, and its environmental impact. It is also studied for its potential use in renewable energy production. '
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buten-2-one : A methyl ketone that is butan-2-one with an unsaturation at position 3. [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 CID6570
CHEMBL ID1600824
CHEBI ID48058
MeSH IDM0161817

Synonyms (91)

Synonym
STL299803
methyl vinyl ketone
wln: 1v1u1
1-propen-3-one
vinyl methyl ketone
ketone, methyl vinyl
78-94-4
methyl ethenyl ketone
3-butene-2-one
1-buten-3-one
3-buten-2-one
nsc4853
acetone, methylene-
methylvinyl ketone
2-butenone
methylvinylketon
butenone
methyl-vinyl-cetone
nsc-4853
but-3-en-2-one
inchi=1/c4h6o/c1-3-4(2)5/h3h,1h2,2h
NCGC00091118-01
einecs 201-160-6
nsc 4853
methyl-vinyl-cetone [french]
methylvinylketon [german]
un1251
ai3-16048
ccris 3423
methylvinylketone
hsdb 716
delta(sup 3)-2-butenone
3-buten-2-one, contains 0.3-1.0% hydroquinone as stabilizer, technical grade, 90%
3-buten-2-one, contains 0.5% hydroquinone and 0.1% acetic acid as stabilizer, 99%
ch2=chcoch3
3-butenone-2
methylvinylcetone
methylene acetone
CHEBI:48058 ,
gamma-oxo-alpha-butylene
acetyl ethylene
delta(3)-2-butenone
buten-2-one
M-6580
3-oxo-1-butene
AKOS000120352
NCGC00091118-02
LMFA12000018
dtxcid205671
tox21_200363
NCGC00257917-01
dtxsid3025671 ,
cas-78-94-4
M0460
methgl vinyl ketone
ec 201-160-6
unii-ar7642i1mp
ar7642i1mp ,
methyl vinyl ketone, stabilized
methyl vinyl ketone, stabilized [un1251] [poison]
C20701
but-1-en-3-one
3-oxobutene
un-1251
methyl vinyl ketone [mi]
.delta.-oxo-.alpha.-butylene
.delta.3-2-butenone
but-3-enone
3-oxo-but-1-ene
methylvinyl-ketone
methyl-vinylketone
methly vinyl ketone
metyl vinyl ketone
methyl-vinyl-ketone
3-oxo-l-butene
1-butene-3-one
3-butenone
methyl vinylketone
CHEMBL1600824 ,
un 1251
3-butenen-2-one
.gamma.-oxo-.alpha.-butylene
mfcd00008777
25038-87-3
3-buten-2-one, purum, >=95.0% (gc)
g-oxo-a-butylene
BCP24759
Q417525
bdbm50245462
F71092
EN300-19794

Research Excerpts

Toxicity

ExcerptReferenceRelevance
"Acrolein is a highly toxic environmental pollutant that readily alkylates the epsilon-amino group of lysine residues in proteins."( Differences in lysine adduction by acrolein and methyl vinyl ketone: implications for cytotoxicity in cultured hepatocytes.
Burcham, PC; Kaminskas, LM; Pyke, SM, 2005
)
0.33
" Recent mixture studies with soft electrophiles have suggested that agents with less-than fully time-dependent toxicity (TDT) may actually induce toxicity by more than one mode of toxic action within the same series of concentrations."( Time-dependence in mixture toxicity with soft-electrophiles: 2. Effects of relative reactivity level on time-dependent toxicity and combined effects for selected Michael acceptors.
Allen, JL; Dawson, DA; Pöch, G; Schultz, TW, 2008
)
0.35
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (2)

ClassDescription
methyl ketoneA ketone of formula RC(=O)CH3 (R =/= H).
enoneAn alpha,beta-unsaturated ketone of general formula R(1)R(2)C=CR(3)-C(=O)R(4) (R(4) =/= H) in which the C=O function is conjugated to a C=C double bond at the alpha,beta position.
[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 (4)

PathwayProteinsCompounds
(3E)-4,8-dimethylnona-1,3,7-triene biosynthesis011
detoxification of reactive carbonyls in chloroplasts422
(3E)-4,8-dimethylnona-1,3,7-triene biosynthesis I212
(E,E)-4,8,12-trimethyltrideca-1,3,7,11-tetraene biosynthesis27
(3E)-4,8-dimethylnona-1,3,7-triene biosynthesis111

Protein Targets (5)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
RAR-related orphan receptor gammaMus musculus (house mouse)Potency0.00840.006038.004119,952.5996AID1159521
aldehyde dehydrogenase 1 family, member A1Homo sapiens (human)Potency19.95260.011212.4002100.0000AID1030
progesterone receptorHomo sapiens (human)Potency53.21080.000417.946075.1148AID1346795
glucocorticoid receptor [Homo sapiens]Homo sapiens (human)Potency60.23710.000214.376460.0339AID720692
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency26.66860.003041.611522,387.1992AID1159552
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (1)

Assay IDTitleYearJournalArticle
AID1469831Inhibition of [3H]dopamine uptake at DAT in rat brain striatal synaptosomes by liquid scintillation counting analysis2017Journal of medicinal chemistry, 02-09, Volume: 60, Issue:3
Covalent Modifiers: A Chemical Perspective on the Reactivity of α,β-Unsaturated Carbonyls with Thiols via Hetero-Michael Addition Reactions.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (82)

TimeframeStudies, This Drug (%)All Drugs %
pre-19905 (6.10)18.7374
1990's4 (4.88)18.2507
2000's35 (42.68)29.6817
2010's31 (37.80)24.3611
2020's7 (8.54)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 43.61

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 Index43.61 (24.57)
Research Supply Index4.44 (2.92)
Research Growth Index5.17 (4.65)
Search Engine Demand Index63.56 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (43.61)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews2 (2.38%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other82 (97.62%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]