CHEBI:15541 - stearoyl-CoA

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ChEBI Name stearoyl-CoA
ChEBI ID CHEBI:15541
Definition A long-chain fatty acyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of stearic acid.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:9256, CHEBI:15107, CHEBI:26754
Supplier Information No supplier information found for this compound.
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Stearoyl-CoA is a coenzyme involved in the metabolism of fatty acids. Stearoyl-CoA is an 18-carbon long fatty acyl-CoA chain that participates in an unsaturation reaction. The reaction is catalyzed by the enzyme stearoyl-CoA desaturase, which is located in the endoplasmic reticulum. It forms a cis-double bond between the ninth and tenth carbons within the chain to form the product oleoyl-CoA.
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Formula C39H70N7O17P3S
Net Charge 0
Average Mass 1034.000
Monoisotopic Mass 1033.37618
InChI InChI=1S/C39H70N7O17P3S/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-30(48)67-23-22-41-29(47)20-21-42-37(51)34(50)39(2,3)25-60-66(57,58)63-65(55,56)59-24-28-33(62-64(52,53)54)32(49)38(61-28)46-27-45-31-35(40)43-26-44-36(31)46/h26-28,32-34,38,49-50H,4-25H2,1-3H3,(H,41,47)(H,42,51)(H,55,56)(H,57,58)(H2,40,43,44)(H2,52,53,54)/t28-,32-,33-,34+,38-/m1/s1
InChIKey SIARJEKBADXQJG-LFZQUHGESA-N
SMILES CCCCCCCCCCCCCCCCCC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
Metabolite of Species Details
Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed
Escherichia coli (NCBI:txid562) See: PubMed
Roles Classification
Chemical Role(s): acyl donor
Any donor that can transfer acyl groups between molecular entities.
(via acyl-CoA )
Biological Role(s): Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing stearoyl-CoA (CHEBI:15541) has functional parent octadecanoic acid (CHEBI:28842)
stearoyl-CoA (CHEBI:15541) has role Escherichia coli metabolite (CHEBI:76971)
stearoyl-CoA (CHEBI:15541) has role mouse metabolite (CHEBI:75771)
stearoyl-CoA (CHEBI:15541) is a 11,12-saturated fatty acyl-CoA (CHEBI:85348)
stearoyl-CoA (CHEBI:15541) is a long-chain fatty acyl-CoA (CHEBI:33184)
stearoyl-CoA (CHEBI:15541) is a saturated fatty acyl-CoA (CHEBI:231546)
stearoyl-CoA (CHEBI:15541) is conjugate acid of stearoyl-CoA(4−) (CHEBI:57394)
Incoming stearoyl-CoA(4−) (CHEBI:57394) is conjugate base of stearoyl-CoA (CHEBI:15541)
IUPAC Name
3'-phosphoadenosine 5'-(3-{(3R)-3-hydroxy-2,2-dimethyl-4-[(3-{[2-(octadecanoylsulfanyl)ethyl]amino}-3-oxopropyl)amino]-4-oxobutyl} dihydrogen diphosphate)
Synonyms Sources
C18:0-CoA ChEBI
C18:0-coenzyme A ChEBI
octadecanoyl-CoA ChEBI
octadecanoyl-coenzyme A ChEBI
S-stearoyl-CoA ChEBI
S-stearoylcoenzyme A ChemIDplus
Stearoyl-CoA KEGG COMPOUND
stearoyl-coenzyme A ChEBI
Stearyl coenzyme A KEGG COMPOUND
Stearyl-CoA KEGG COMPOUND
Manual Xrefs Databases
84957 ChemSpider
C00412 KEGG COMPOUND
FDB022431 FooDB
HMDB0001114 HMDB
LMFA07050369 LIPID MAPS
ST9 PDBeChem
Stearoyl-CoA Wikipedia
View more database links
Registry Numbers Types Sources
362-66-3 CAS Registry Number KEGG COMPOUND
362-66-3 CAS Registry Number ChemIDplus
8033851 Reaxys Registry Number Reaxys
Citations
Kikuchi K, Tsukamoto H (2020)
Stearoyl-CoA desaturase and tumorigenesis.
Chemico-biological interactions 316, 108917 [PubMed:31838050]
[show Abstract]
O'Neill LM, Guo CA, Ding F, Phang YX, Liu Z, Shamsuzzaman S, Ntambi JM (2020)
Stearoyl-CoA Desaturase-2 in Murine Development, Metabolism, and Disease.
International journal of molecular sciences 21, E8619 [PubMed:33207603]
[show Abstract]
Olichwier A, Balatskyi VV, Wolosiewicz M, Ntambi JM, Dobrzyn P (2020)
Interplay between Thyroid Hormones and Stearoyl-CoA Desaturase 1 in the Regulation of Lipid Metabolism in the Heart.
International journal of molecular sciences 22, E109 [PubMed:33374300]
[show Abstract]
Zhang Y, Zheng Y, Wang X, Qiu J, Liang C, Cheng G, Wang H, Zhao C, Yang W, Zan L, Li A (2020)
Bovine Stearoyl-CoA Desaturase 1 Promotes Adipogenesis by Activating the PPARγ Receptor.
Journal of agricultural and food chemistry 68, 12058-12066 [PubMed:33052678]
[show Abstract]
Gao Y, Zhang H, Fan M, Jia C, Shi L, Pan X, Cao P, Zhao X, Chang W, Li M (2020)
Structural insights into catalytic mechanism and product delivery of cyanobacterial acyl-acyl carrier protein reductase.
Nature communications 11, 1525 [PubMed:32251275]
[show Abstract]
Chen X, Chen J, Yan B, Zhang W, Guddat LW, Liu X, Rao Z (2020)
Structural basis for the broad substrate specificity of two acyl-CoA dehydrogenases FadE5 from mycobacteria.
Proceedings of the National Academy of Sciences of the United States of America 117, 16324-16332 [PubMed:32601219]
[show Abstract]
Bai Y, McCoy JG, Levin EJ, Sobrado P, Rajashankar KR, Fox BG, Zhou M (2015)
X-ray structure of a mammalian stearoyl-CoA desaturase.
Nature 524, 252-256 [PubMed:26098370]
[show Abstract]
Wang H, Klein MG, Zou H, Lane W, Snell G, Levin I, Li K, Sang BC (2015)
Crystal structure of human stearoyl-coenzyme A desaturase in complex with substrate.
Nature structural & molecular biology 22, 581-585 [PubMed:26098317]
[show Abstract]
Fujihashi M, Nakatani T, Hirooka K, Matsuoka H, Fujita Y, Miki K (2014)
Structural characterization of a ligand-bound form of Bacillus subtilis FadR involved in the regulation of fatty acid degradation.
Proteins 82, 1301-1310 [PubMed:24356978]
[show Abstract]
Høvik KE, Spydevold OS, Bremer J (1997)
Thia fatty acids as substrates and inhibitors of stearoyl-CoA desaturase.
Biochimica et biophysica acta 1349, 251-256 [PubMed:9434139]
[show Abstract]
Ntambi JM (1995)
The regulation of stearoyl-CoA desaturase (SCD).
Progress in lipid research 34, 139-150 [PubMed:7480063]
[show Abstract]
Boiron F, Heape MA, Cassagne C (1984)
Assay of stearoyl-CoA synthesis in microsomes from normal and Trembler mouse sciatic nerves.
Neuroscience letters 48, 7-12 [PubMed:6472736]
[show Abstract]
Last Modified
07 June 2024
General Comment
2011-05-13 A long-chain fatty acyl-CoA thioester that acts as an intermediate metabolite in the biosynthesis of monounsaturated fatty acids.