Page last updated: 2024-11-05

2,3-hexanedione

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

Description

hexane-2,3-dione : An alpha-diketone that is hexane substituted by oxo groups at positions 2 and 3 respectively. [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 CID19707
CHEMBL ID3187497
CHEBI ID87583
SCHEMBL ID108066
MeSH IDM0127328

Synonyms (46)

Synonym
LS-13150
acetylbutyryl
nsc31665
nsc-31665
3848-24-6
2,3-hexanedione
nsc 31665
methyl propyl diketone
brn 1699896
butyryl acetyl
einecs 223-350-8
ai3-35989
fema no. 2558
acetyl butyryl
2,3-hexanedione, >=95%, fg
2,3-hexanedione, technical grade, 90%
hexane-2,3-dione
LMFA12000247
cas-3848-24-6
tox21_302349
dtxcid0027066
NCGC00256020-01
dtxsid2047066 ,
hexanedione
559anr3nvs ,
unii-559anr3nvs
FT-0609744
2,3-hexanodione;methyl propyl diketone;methylpropyldiketone
AKOS015899028
SCHEMBL108066
2,3-hexanedione [fhfi]
hexanedione, 2,3-
2,3-hexandione
chebi:87583 ,
CHEMBL3187497
mfcd00009398
2,3-hexanedione, analytical standard
2,3-hexanedione, natural, 96%, fg
fema 2558
methyl propyl glyoxal
2,3-hexanodione
CS-0258819
Q11186388
A846404
EN300-7149590
2,3-hexanedione; acetylbutyryl; nsc 31665

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" These alpha-diketones also display a degree of toxic selectivity towards neuroblastoma cells, which may have therapeutic implications."( A comparison of the apoptotic and cytotoxic effects of hexanedione derivatives on human non-neuronal lines and the neuroblastoma line SH-SY5Y.
Coleman, MD; Griffiths, HR; Woehrling, EK; Zilz, TR, 2008
)
0.35
"Occupational exposure to 2,3-butanedione (BD) vapors has been associated with severe respiratory disease leading to the use of potentially toxic substitutes."( Chemical Reactivity and Respiratory Toxicity of the α-Diketone Flavoring Agents: 2,3-Butanedione, 2,3-Pentanedione, and 2,3-Hexanedione.
Bousquet, RW; Flake, GP; Gwinn, WM; Johnson, CL; Jokinen, MP; Morgan, DL; Price, HC, 2016
)
0.64
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
metaboliteAny intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
[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
alpha-diketoneA diketone that has its two ketone functionalities on adjacent atoms.
[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]

Bioassays (3)

Assay IDTitleYearJournalArticle
AID1347082qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lassa (LASV) Arenavirus: LASV Primary Screen - GLuc reporter signal2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID1347086qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lymphocytic Choriomeningitis Arenaviruses (LCMV): LCMV Primary Screen - GLuc reporter signal2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID1347083qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lassa (LASV) Arenavirus: Viability assay - alamar blue signal for LASV Primary Screen2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (12)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (8.33)18.7374
1990's2 (16.67)18.2507
2000's3 (25.00)29.6817
2010's5 (41.67)24.3611
2020's1 (8.33)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 30.71

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 Index30.71 (24.57)
Research Supply Index2.56 (2.92)
Research Growth Index4.92 (4.65)
Search Engine Demand Index36.71 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (30.71)

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%
Other12 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]