Page last updated: 2024-12-05

diethyl ketone

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

Description

Diethyl ketone, also known as 3-pentanone, is a colorless liquid with a pungent odor. It is a common organic solvent and is used in the production of pharmaceuticals, resins, and other chemicals. Diethyl ketone can be synthesized through various methods, including the oxidation of 3-pentanol or the reaction of ethyl magnesium bromide with ethyl acetate. Research on diethyl ketone focuses on its potential applications in organic synthesis, its use as a model compound for studying ketone reactivity, and its environmental impact. Its effects include being a potential irritant to the skin and respiratory system.'

diethyl ketone: RN given refers to unlabeled parent cpd [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

pentan-3-one : A pentanone that is pentane carrying an oxo group at position 3. It has been isolated from Triatoma brasiliensis and Triatoma infestans. [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 CID7288
CHEMBL ID45315
CHEBI ID87755
MeSH IDM0089240

Synonyms (68)

Synonym
diethylcetone
nsc8653
metacetone
propione
methacetone
diethyl ketone
ethyl ketone
dimethylacetone
wln: 2v2
nsc-8653
3-pentanone
dek
96-22-0
pentanone-3
hsdb 5301
ai3-24337
einecs 202-490-3
un1156
ethyl propionyl
nsc 8653
diethylcetone [french]
LMFA12000001
pentan-3-one
diethylketone
inchi=1/c5h10o/c1-3-5(6)4-2/h3-4h2,1-2h
3-pentanone, >=99%
NCGC00166068-01
3-pentanone, reagentplus(r), >=99%
chebi:87755 ,
CHEMBL45315
P0061
AKOS000119714
A845564
NCGC00166068-02
1-pentan-3-one
ec 202-490-3
9slz98m9nk ,
diethyl ketone [un1156] [flammable liquid]
unii-9slz98m9nk
tox21_200677
dtxcid301820
dtxsid6021820 ,
cas-96-22-0
NCGC00258231-01
STL281851
FT-0616299
BBL027755
diethyl ketone [mi]
3-pentanone [hsdb]
un 1156
1,3-dimethylacetone
(c2h5)2co
diethylketon
3-pentanon
di-ethyl ketone
ethyl ethyl ketone
3-penta none
F0001-2290
mfcd00009320
3-pentanone, for hplc, 96%
3-pentanone, analytical standard
3-pentanone, reagentplus(r), >=99.0% (gc)
3-pentanone-1,1,1,5,5,5-d6
3-pentanone 100 microg/ml in acetonitrile
Q223112
AMY11060
EN300-20108
Z104476878
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
animal metaboliteAny eukaryotic metabolite produced during a metabolic reaction in animals that include diverse creatures from sponges, insects to mammals.
[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
pentanoneAny ketone that is pentane substituted by an oxo group at unspecified 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 (1)

PathwayProteinsCompounds
detoxification of reactive carbonyls in chloroplasts422

Protein Targets (5)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Chain A, MAJOR APURINIC/APYRIMIDINIC ENDONUCLEASEHomo sapiens (human)Potency35.48130.003245.467312,589.2998AID2517
Chain A, TYROSYL-DNA PHOSPHODIESTERASEHomo sapiens (human)Potency14.12540.004023.8416100.0000AID485290
Chain A, Putative fructose-1,6-bisphosphate aldolaseGiardia intestinalisPotency14.09190.140911.194039.8107AID2451
phosphopantetheinyl transferaseBacillus subtilisPotency56.23410.141337.9142100.0000AID1490
vitamin D3 receptor isoform VDRAHomo sapiens (human)Potency89.12510.354828.065989.1251AID504847
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (1)

Assay IDTitleYearJournalArticle
AID212400Toxicity determined using Tadpole Narcosis Test1991Journal of medicinal chemistry, May, Volume: 34, Issue:5
Using theoretical descriptors in quantitative structure-activity relationships: some toxicological indices.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (13)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (15.38)18.7374
1990's1 (7.69)18.2507
2000's1 (7.69)29.6817
2010's9 (69.23)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: 54.82

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 Index54.82 (24.57)
Research Supply Index2.64 (2.92)
Research Growth Index5.12 (4.65)
Search Engine Demand Index80.79 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (54.82)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (7.69%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other12 (92.31%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]