Page last updated: 2024-11-05

2-tridecanone

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

Description

2-tridecanone is a ketone with the molecular formula C13H26O. It is a colorless liquid with a strong, floral odor. 2-tridecanone is a component of the scent of several plants, including orchids and roses. It is also found in some insects, such as the honeybee. 2-tridecanone is used in the fragrance industry as a synthetic fragrance ingredient. It is also used as a food flavoring agent. 2-tridecanone has been studied for its potential to attract insects and other animals. It has also been shown to have some biological activity, such as inhibiting the growth of certain bacteria.'

tridecan-2-one : A methyl ketone that is tridecane in which the methylene hydrogens at position 2 are replaced by an oxo group. [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 CID11622
CHEMBL ID480097
CHEBI ID77928
SCHEMBL ID119126
MeSH IDM0054337

Synonyms (50)

Synonym
n-butyl-n-octyl ketone
unii-5q35vhx26k
5q35vhx26k ,
tridecanone
nsc-14763
tridecan-2-one
methyl undecyl ketone
2-tridecanone
593-08-8
2-tridecankje
mathyl undecyl kepoje
nsc14763
fema no. 3388
hendecyl methyl ketone
nsc 14763
ai3-04238
einecs 209-784-0
2-tridecanone (natural)
2-tridecanone, >=96%, fg
2-tridecanone, 99%
T0415
CHEMBL480097
chebi:77928 ,
A832256
AKOS009158653
LMFA12000058
tox21_301838
dtxcid302070
dtxsid4022070 ,
NCGC00255260-01
cas-593-08-8
2td ,
FT-0613458
2-tridecanone [fhfi]
2-tridecanone [fcc]
SCHEMBL119126
methyl n-undecyl ketone
tridecanone-2
W-105331
2-tridecanone, >=98%, natural, fg
2-tridecanone, analytical standard
mfcd00008968
2-tridecanone, purum, >=97.0% (gc)
D78019
fema 3388
Q27147536
dimethoxy methyldopa hydrochloride(dmmd)
CS-W010527
HY-W009811
PD158263

Research Excerpts

Toxicity

2-Tridecanone was found not to be Persistent, Bioaccumulative, and Toxic (PBT) as per the International Fragrance Association.

ExcerptReferenceRelevance
" The environmental endpoints were evaluated; 2-Tridecanone was found not to be Persistent, Bioaccumulative, and Toxic (PBT) as per the International Fragrance Association (IFRA) Environmental Standards, and its risk quotients, based on its current volume of use in Europe and North America (i."( RIFM fragrance ingredient safety assessment, 2-tridecanone, CAS Registry Number 593-08-8.
Api, AM; Belsito, D; Botelho, D; Bruze, M; Burton, GA; Cancellieri, MA; Chon, H; Dagli, ML; Date, M; Dekant, W; Deodhar, C; Fryer, AD; Jones, L; Joshi, K; Kumar, M; Lapczynski, A; Lavelle, M; Lee, I; Liebler, DC; Moustakas, H; Na, M; Penning, TM; Ritacco, G; Romine, J; Sadekar, N; Schultz, TW; Selechnik, D; Siddiqi, F; Sipes, IG; Sullivan, G; Thakkar, Y; Tokura, Y, 2022
)
1.24

Dosage Studied

ExcerptRelevanceReference
" Using dose-response relationships assessed earlier (Chatzivasileiadis and Sabelis, 1997, 1998), we estimated that the number of mite-trichome contacts causing 50% mortality per day is equal to 88 on a tomato stem, whereas it equals 70 for another strain of spider mites collected from cucumber."( Accumulation and turnover of 2-tridecanone in Tetranychus urticae and its consequences for resistance of wild and cultivated tomatoes.
Boon, JJ; Chatzivasileiadis, EA; Sabelis, MW, 1999
)
0.59
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
plant metaboliteAny eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
flavouring agentA food additive that is used to added improve the taste or odour of a food.
[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
methyl ketoneA ketone of formula RC(=O)CH3 (R =/= H).
[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]

Protein Targets (3)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
estrogen nuclear receptor alphaHomo sapiens (human)Potency24.06230.000229.305416,493.5996AID743075; AID743079
peroxisome proliferator-activated receptor deltaHomo sapiens (human)Potency43.64120.001024.504861.6448AID743215
vitamin D (1,25- dihydroxyvitamin D3) receptorHomo sapiens (human)Potency43.64120.023723.228263.5986AID743223
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (11)

Assay IDTitleYearJournalArticle
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.
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.
AID377127Antiplatelet activity against rabbit platelets assessed as inhibition of arachidonic acid-induced platelet aggregation at 20 ug/ml preincubated for 3 mins by turbidimetric method1999Journal of natural products, Jun, Volume: 62, Issue:6
Chemical constituents and biological activities of the fruit of Zanthoxylum integrifoliolum.
AID1082317Nematicidal activity against second-stage juvenile Meloidogyne javanica (root-knot nematode) assessed as paralysis measured after 1 hr2011Journal of agricultural and food chemistry, Jul-13, Volume: 59, Issue:13
Aliphatic ketones from Ruta chalepensis (Rutaceae) induce paralysis on root knot nematodes.
AID377131Antiplatelet activity against rabbit platelets assessed as inhibition of collagen-induced platelet aggregation at 100 ug/ml preincubated for 3 mins by turbidimetric method1999Journal of natural products, Jun, Volume: 62, Issue:6
Chemical constituents and biological activities of the fruit of Zanthoxylum integrifoliolum.
AID1082319Nematicidal activity against second-stage juvenile Meloidogyne incognita (root-knot nematode) assessed as paralysis measured after 1 hr2011Journal of agricultural and food chemistry, Jul-13, Volume: 59, Issue:13
Aliphatic ketones from Ruta chalepensis (Rutaceae) induce paralysis on root knot nematodes.
AID1082316Nematicidal activity against second-stage juvenile Meloidogyne javanica (root-knot nematode) assessed as paralysis measured after 1 day2011Journal of agricultural and food chemistry, Jul-13, Volume: 59, Issue:13
Aliphatic ketones from Ruta chalepensis (Rutaceae) induce paralysis on root knot nematodes.
AID377132Antiplatelet activity against rabbit platelets assessed as inhibition of collagen-induced platelet aggregation at 50 ug/ml preincubated for 3 mins by turbidimetric method1999Journal of natural products, Jun, Volume: 62, Issue:6
Chemical constituents and biological activities of the fruit of Zanthoxylum integrifoliolum.
AID1659751Agonist activity at TRPA1 (unknown origin) at 1000 uM relative to AITC2020Bioorganic & medicinal chemistry letters, 06-01, Volume: 30, Issue:11
Identification of a new class of non-electrophilic TRPA1 agonists by a structure-based virtual screening approach.
AID1082318Nematicidal activity against second-stage juvenile Meloidogyne incognita (root-knot nematode) assessed as paralysis measured after 1 day2011Journal of agricultural and food chemistry, Jul-13, Volume: 59, Issue:13
Aliphatic ketones from Ruta chalepensis (Rutaceae) induce paralysis on root knot nematodes.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (40)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (5.00)18.7374
1990's3 (7.50)18.2507
2000's6 (15.00)29.6817
2010's22 (55.00)24.3611
2020's7 (17.50)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 32.24

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 Index32.24 (24.57)
Research Supply Index3.71 (2.92)
Research Growth Index5.20 (4.65)
Search Engine Demand Index35.22 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (32.24)

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%
Other40 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]