Page last updated: 2024-12-11

oleoyl-coenzyme a

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

Description

oleoyl-coenzyme A: RN given refers to (Z)-isomer [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID5497111
CHEBI ID15534
MeSH IDM0068464

Synonyms (51)

Synonym
gtpl2386
3'-phosphoadenosine 5'-{3-[(3r)-3-hydroxy-2,2-dimethyl-4-({3-[(2-{[(9z)-octadec-9-enoyl]sulfanyl}ethyl)amino]-3-oxopropyl}amino)-4-oxobutyl] dihydrogen diphosphate}
cis-delta(9)-octadecenoyl-coenzyme a
cis-9-octadecenoyl-coenzyme a
(9z)-octadec-9-enoyl-coenzyme a
cis-9-octadecenoyl-coa
s-oleoyl-coa
s-[(9z)-octadec-9-enoyl]-coenzyme a
s-oleoylcoenzyme a
oleoyl-coenzyme a
cis-delta(9)-octadecenoyl-coa
CHEBI:15534
s-[(9z)-octadec-9-enoyl]-coa
coenzyme a, oleoyl-
(9z)-octadec-9-enoyl-coa
coenzyme a cis-9-octadecenoate
9-octadecenoyl-coenzyme a
o-beta-d-ribofuranosyl]-
9-octadecenoyl-coa
coenzyme a, s-(9z)-9-octadecenoate (9ci)
coenzyme a, s-9-octadecenoate, (z)-
18:1, oleoyl-coa 9-[5-o-[hydroxy[[hydroxy[[(3r)-3-hydroxy-2,2-dimethyl-4-oxo-4-[[3-oxo-3-[[2-[[(9z)-1-oxo-9-octadecenyl]thio]ethyl]amino]propyl]amino]butyl]oxy]phosphinyl]oxy]phosphinyl]-3-o-phosphon
coenzyme a, s-oleate (7ci,8ci)
oleyl coenzyme a
1716-06-9
oleoyl coenzyme a
(9z)-octadecenoyl-coa
oleoyl-coa ,
C00510
[14c]oleoyl-coa
bdbm27948
{[(2r,3s,4r,5r)-5-(6-amino-9h-purin-9-yl)-4-hydroxy-2-({[hydroxy({hydroxy[(3r)-3-hydroxy-2,2-dimethyl-3-{[2-({2-[(9z)-octadec-9-enoylsulfanyl]ethyl}carbamoyl)ethyl]carbamoyl}propoxy]phosphoryl}oxy)phosphoryl]oxy}methyl)oxolan-3-yl]oxy}phosphonic acid
[14c]oleyl-coa
[14c] oleoyl coenzyme a
cis-9-octadecenoyl coenzyme a
s-[2-[3-[[(2r)-4-[[[(2r,3s,4r,5r)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-2-hydroxy-3,3-dimethylbutanoyl]amino]propanoylamino]ethyl] (z)-octadec-9-enethioate
spv646a327 ,
einecs 216-998-8
unii-spv646a327
s-{(3r,5r,9r)-1-[(2r,3s,4r,5r)-5-(6-amino-9h-purin-9-yl)-4-hydroxy-3-(phosphonooxy)tetrahydrofuran-2-yl]-3,5,9-trihydroxy-8,8-dimethyl-3,5-dioxido-10,14-dioxo-2,4,6-trioxa-11,15-diaza-3lambda~5~,5lambda~5~-diphosphaheptadecan-17-yl} (9z)-octadec-9-enethio
coenzyme a, s-(9z)-9-octadecenoate
coenzyme a, s-oleate
oleoyl coenzyme a lithium salt
LMFA07050356
J-012171
octadecenoyl-coa (n-c18:1coa)
Q27088172
DTXSID601318533
coenzyme a oleate
HY-109591
CS-0032765

Research Excerpts

Bioavailability

ExcerptReferenceRelevance
" Pharmacokinetic studies indicated that RP 64477 were very poorly absorbed following oral administration to rats."( RP 64477: a potent inhibitor of acyl-coenzyme A:cholesterol O-acyltransferase with low systemic bioavailability.
Bello, AA; Bright, C; Burton, BJ; Bush, RC; Casey, JH; Dron, DI; Facchini, V; Joannou, PP; Parrott, DP; Riddell, D; Roberts, SA; Williams, RJ, 1996
)
0.29

Dosage Studied

ExcerptRelevanceReference
"5 to 2 microM, these FFA metabolites stimulated ATP synthesis; however, above 5 microM, there was a dose-response inhibition of ATP synthesis."( Deleterious action of FA metabolites on ATP synthesis: possible link between lipotoxicity, mitochondrial dysfunction, and insulin resistance.
Abdul-Ghani, MA; Balas, B; Chang, Z; Chavez, AO; DeFronzo, RA; Folli, F; Jani, R; Liu, Y; Molina-Carrion, M; Monroy, A; Muller, FL; Tripathy, D; Van Remmen, H; Zuo, P, 2008
)
0.35
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
Escherichia coli metaboliteAny bacterial metabolite produced during a metabolic reaction in Escherichia coli.
mouse metaboliteAny mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
[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
octadecenoyl-CoAAny unsaturated fatty acyl-CoA in which the S-acyl moiety contains 18 carbons and 1 double bond.
[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 (6)

PathwayProteinsCompounds
Metabolism14961108
Metabolism of lipids500463
Fatty acid metabolism113203
Fatty acyl-CoA biosynthesis1635
Omega-9 fatty acid synthesis226
Mitochondrial beta-oxidation064

Bioassays (2)

Assay IDTitleYearJournalArticle
AID1346519Mouse Kir2.1 (Inwardly rectifying potassium channels)2005The Journal of biological chemistry, Sep-02, Volume: 280, Issue:35
Long chain CoA esters as competitive antagonists of phosphatidylinositol 4,5-bisphosphate activation in Kir channels.
AID1346519Mouse Kir2.1 (Inwardly rectifying potassium channels)2006The Journal of physiology, Sep-01, Volume: 575, Issue:Pt 2
Cytoplasmic accumulation of long-chain coenzyme A esters activates KATP and inhibits Kir2.1 channels.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (166)

TimeframeStudies, This Drug (%)All Drugs %
pre-199055 (33.13)18.7374
1990's50 (30.12)18.2507
2000's36 (21.69)29.6817
2010's23 (13.86)24.3611
2020's2 (1.20)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 30.31

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 Index30.31 (24.57)
Research Supply Index5.14 (2.92)
Research Growth Index4.41 (4.65)
Search Engine Demand Index42.09 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (30.31)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews2 (1.18%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other168 (98.82%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]