Page last updated: 2024-11-05
ethyl oenanthate
Description
Ethyl oenanthate, also known as ethyl heptanoate, is a colorless liquid ester with a fruity, wine-like aroma. It is naturally found in various fruits, wines, and cheeses. It is synthesized through the reaction of heptanoic acid with ethanol in the presence of a catalyst. Ethyl oenanthate is used as a flavoring agent in food and beverages, particularly in artificial fruit flavors, and is also used in perfumes. It is also employed as a solvent in some chemical processes. Studies on ethyl oenanthate focus on its sensory properties, its role in food chemistry, and its potential applications in various industries.'
ethyl heptanoate : The fatty acid ethyl ester of heptanoic acid. [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 Source | ID |
PubMed CID | 7797 |
CHEMBL ID | 3184220 |
CHEBI ID | 86618 |
SCHEMBL ID | 1585 |
MeSH ID | M0100619 |
Synonyms (65)
Synonym |
fema no. 2437 |
ai3-24251 |
ethyl heptanoate (natural) |
einecs 203-382-9 |
ccris 1344 |
brn 1752311 |
nsc 8891 |
ethyl enantate |
ethyl oenanthylate |
oenanthic ether |
ethyl heptanoate |
nsc8891 |
oleum vitis viniferae |
106-30-9 |
ethyl heptoate |
heptanoic acid, ethyl ester |
ethyl n-heptanoate |
enanthylic ether |
ethyl enanthate |
aether oenanthicus |
ethyl heptylate |
ethyl oenanthate |
ethyl heptanoate, natural, >=98%, fg |
ethyl heptanoate, >=98%, fcc, fg |
ethyl heptanoate, reagentplus(r), 99% |
BMSE000550 |
heptanoic acid ethyl ester |
H0031 |
enanthic acid ethyl ester |
A801415 |
NCGC00248014-01 |
cas-106-30-9 |
dtxcid9020112 |
dtxsid1040112 , |
tox21_300382 |
NCGC00254287-01 |
unii-45r404y5x8 |
45r404y5x8 , |
FT-0626189 |
AKOS015907945 |
ethyl oenanthate [mi] |
ethyl heptanoate [fcc] |
ethyl heptanoate [fhfi] |
ethyl n-heptoate |
SCHEMBL1585 |
hexane-6-carboxylic acid ethyl ester |
ethyl ester of heptanoic acid |
CHEMBL3184220 |
chebi:86618 , |
mfcd00009538 |
J-001569 |
LMFA07010984 |
ethyl heptanoate, purum, >=96.0% (gc) |
ethyl heptanoate, analytical standard |
ethyl heptanoate, vetec(tm) reagent grade, 98% |
heptanoic acid-ethyl ester |
ethyl heptoic acid |
ethyl heptanoic acid |
ethyl n-heptanoic acid |
Q419765 |
E75824 |
ethyl2-(4-chlorophenyl)-4-methyl-1,3-thiazole-5-carboxylate |
ethyl heptanoate(heptanoic acid ethyl ester) |
CS-W010893 |
HY-W010177 |
Roles (1)
Role | Description |
metabolite | Any 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)
Class | Description |
fatty acid ethyl ester | A fatty acid ester that is the carboxylic ester obtained by the formal condensation of a fatty acid with ethanol. |
[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 (4)
Potency Measurements
Bioassays (3)
Assay ID | Title | Year | Journal | Article |
AID1347083 | qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lassa (LASV) Arenavirus: Viability assay - alamar blue signal for LASV Primary Screen | 2020 | Antiviral research, 01, Volume: 173 | A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity. |
AID1347086 | qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lymphocytic Choriomeningitis Arenaviruses (LCMV): LCMV Primary Screen - GLuc reporter signal | 2020 | Antiviral research, 01, Volume: 173 | A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity. |
AID1347082 | qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lassa (LASV) Arenavirus: LASV Primary Screen - GLuc reporter signal | 2020 | Antiviral research, 01, Volume: 173 | A 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 (6)
Timeframe | Studies, This Drug (%) | All Drugs % |
pre-1990 | 1 (16.67) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 2 (33.33) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Market Indicators
Research Demand Index: 23.15
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.
Metric | This Compound (vs All) |
---|
Research Demand Index | 23.15 (24.57) | Research Supply Index | 1.95 (2.92) | Research Growth Index | 4.51 (4.65) | Search Engine Demand Index | 21.17 (26.88) | Search Engine Supply Index | 2.00 (0.95) |
| |
Study Types
Publication Type | This drug (%) | All Drugs (%) |
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 6 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |