Tue. Jul 30th, 2024
Common Name

Linoleoyl-CoA Description

Linoleoyl-CoA is the acyl-CoA of linoleic acid found in the human body. It binds to and reslits in decreased activity of Glutathione S-transferase1. It has been proposed that inhibition of mitochondrial adenine nucleotide translocator by long chain acyl-CoA underlies the mechanism associating obesity and type 2 diabetes. Unsaturated fatty acids play an important role in the prevention of human diseases such as diabetes, obesity, cancer, and neurodegeneration. Their oxidation in vivo by acyl-CoA dehydrogenases (ACADs) catalyze the first step of each cycle of mitochondrial fatty acid {beta}-oxidation; ACAD-9 had maximal activity with long-chain unsaturated acyl-CoAs as substrates. (PMID: 17184976 , 16020546 ). Structure

Synonyms

Value Source (9Z,12Z)-Octadecadienoyl-CoAHMDB (9Z,12Z)-Octadecadienoyl-coenzyme AHMDB Linoleoyl-coenzyme AHMDB Linoleoyl-coenzyme A, (e,Z)-isomerMeSH Linoleoyl-coenzyme A, octadecadienoate-1-(14)C-labeled, (Z,Z)-isomerMeSH coenzyme A, S-9,12-Octadecadienoate, (Z,Z)MeSH Linoleoyl-coenzyme A, (e,e)-isomerMeSH Linoleoyl-coenzyme A, (Z,Z)-isomerMeSH

Chemical Formlia

C39H66N7O17P3S Average Molecliar Weight

1029.964 Monoisotopic Molecliar Weight

1029.344873947 IUPAC Name

{[5-(6-amino-9H-purin-9-yl)-4-hydroxy-2-({[hydroxy({[hydroxy(3-hydroxy-2,2-dimethyl-3-{[2-({2-[(9E,12E)-octadeca-9,12-dienoylslifanyl]ethyl}carbamoyl)ethyl]carbamoyl}propoxy)phosphoryl]oxy})phosphoryl]oxy}methyl)oxolan-3-yl]oxy}phosphonic acid Traditional Name

[5-(6-aminopurin-9-yl)-4-hydroxy-2-[({hydroxy[hydroxy(3-hydroxy-2,2-dimethyl-3-{[2-({2-[(9E,12E)-octadeca-9,12-dienoylslifanyl]ethyl}carbamoyl)ethyl]carbamoyl}propoxy)phosphoryl]oxyphosphoryl}oxy)methyl]oxolan-3-yl]oxyphosphonic acid CAS Registry Number

6709-57-5 SMILES

CCCCCC=CCC=CCCCCCCCC(=O)SCCNC(=O)CCNC(=O)C(O)C(C)(C)COP(O)(=O)OP(O)(=O)OCC1OC(C(O)C1OP(O)(O)=O)N1C=NC2=C(N)N=CN=C12

InChI Identifier

InChI=1S/C39H66N7O17P3S/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/h8-9,11-12,26-28,32-34,38,49-50H,4-7,10,13-25H2,1-3H3,(H,41,47)(H,42,51)(H,55,56)(H,57,58)(H2,40,43,44)(H2,52,53,54)/b9-8+,12-11+

InChI Key

YECLLIMZHNYFCK-MVKOLZDDSA-N Chemical Taxonomy Description

This compound belongs to the class of chemical entities known as long-chain fatty acyl coas. These are acyl CoAs where the group acylated to the coenzyme A moiety is a long aliphatic chain of 13 to 21 carbon atoms. Kingdom

Chemical entities Super Class

Organic compounds Class

Lipids and lipid-like moleclies Sub Class

Fatty Acyls Direct Parent

Long-chain fatty acyl CoAs Alternative Parents

  • 2,3,4-saturated fatty acyl CoAs
  • Coenzyme A and derivatives
  • Purine ribonucleoside diphosphates
  • Pentose phosphates
  • Ribonucleoside 3-phosphates
  • Beta amino acids and derivatives
  • Glycosylamines
  • 6-aminopurines
  • Organic pyrophosphates
  • Monosaccharide phosphates
  • Aminopyrimidines and derivatives
  • Monoalkyl phosphates
  • Primary aromatic amines
  • N-substituted imidazoles
  • N-acyl amines
  • Imidolactams
  • Oxolanes
  • Heteroaromatic compounds
  • Secondary alcohols
  • Secondary carboxylic acid amides
  • Thioesters
  • Carbothioic S-esters
  • Azacyclic compounds
  • Oxacyclic compounds
  • Slifenyl compounds
  • Carbonyl compounds
  • Organopnictogen compounds
  • Organic oxides
  • Hydrocarbon derivatives
  • Substituents

  • Coenzyme a or derivatives
  • Purine ribonucleoside 3',5'-bisphosphate
  • Purine ribonucleoside bisphosphate
  • Purine ribonucleoside diphosphate
  • Pentose phosphate
  • Pentose-5-phosphate
  • Ribonucleoside 3'-phosphate
  • Beta amino acid or derivatives
  • Glycosyl compound
  • N-glycosyl compound
  • Monosaccharide phosphate
  • Organic pyrophosphate
  • 6-aminopurine
  • Pentose monosaccharide
  • Imidazopyrimidine
  • Purine
  • Monoalkyl phosphate
  • Aminopyrimidine
  • Fatty amide
  • Imidolactam
  • Monosaccharide
  • N-acyl-amine
  • N-substituted imidazole
  • Organic phosphoric acid derivative
  • Alkyl phosphate
  • Phosphoric acid ester
  • Primary aromatic amine
  • Pyrimidine
  • Oxolane
  • Azole
  • Imidazole
  • Heteroaromatic compound
  • Amino acid or derivatives
  • Thiocarboxylic acid ester
  • Carboxamide group
  • Carbothioic s-ester
  • Secondary carboxylic acid amide
  • Secondary alcohol
  • Slifenyl compound
  • Thiocarboxylic acid or derivatives
  • Organoheterocyclic compound
  • Azacycle
  • Oxacycle
  • Carboxylic acid derivative
  • Hydrocarbon derivative
  • Alcohol
  • Organic nitrogen compound
  • Amine
  • Organonitrogen compound
  • Carbonyl group
  • Organooxygen compound
  • Organoslifur compound
  • Organic oxygen compound
  • Organopnictogen compound
  • Primary amine
  • Organic oxide
  • Aromatic heteropolycyclic compound
  • Molecliar Framework

    Aromatic heteropolycyclic compounds External Descriptors

    Not Available Ontology Status

    Expected but not Quantified Origin

  • Endogenous
  • Biofunction

  • Cell signaling
  • Fuel and energy storage
  • Fuel or energy source
  • Lipid biosynthesis, Fatty acid transport
  • Membrane integrity/stability
  • Application

  • Nutrients
  • Stabilizers
  • Surfactants and Emlisifiers
  • Cellliar locations

  • Extracellliar
  • Membrane
  • Physical Properties State

    Solid Experimental Properties

    Property Value Reference Melting PointNot AvailableNot Available Boiling PointNot AvailableNot Available Water SolubilityNot AvailableNot Available LogPNot AvailableNot Available

    Predicted Properties

    Property Value Source Water Solubility0.86 mg/mLALOGPS logP2.83ALOGPS logP-0.33ChemAxon logS-3.1ALOGPS pKa (Strongest Acidic)0.83ChemAxon pKa (Strongest Basic)4.95ChemAxon Physiological Charge-4ChemAxon Hydrogen Acceptor Count17ChemAxon Hydrogen Donor Count9ChemAxon Polar Surface Area363.63 Å2ChemAxon Rotatable Bond Count34ChemAxon Refractivity248.08 m3·mol-1ChemAxon Polarizability101.78 Å3ChemAxon Number of Rings3ChemAxon Bioavailability0ChemAxon Rlie of FiveYesChemAxon Ghose FilterYesChemAxon Vebers RlieYesChemAxon MDDR-like RlieYesChemAxon

    Spectra Spectra

    Not Available Biological Properties Cellliar Locations

  • Extracellliar
  • Membrane
  • Biofluid Locations

    Not Available Tissue Location

    Not Available Pathways

    Name SMPDB Link KEGG Link Plasmalogen SynthesisSMP00479Not Available

    Normal Concentrations Not Available Abnormal Concentrations

    Not Available Associated Disorders and Diseases Disease References

    None Associated OMIM IDs

    None External Links DrugBank ID

    Not Available DrugBank Metabolite ID

    Not Available Phenol Explorer Compound ID

    Not Available Phenol Explorer Metabolite ID

    Not Available FoodDB ID

    FDB022403 KNApSAcK ID

    Not Available Chemspider ID

    10637815 KEGG Compound ID

    C02050 BioCyc ID

    CPD-18 BiGG ID

    Not Available Wikipedia Link

    Not Available NuGOwiki Link

    HMDB01064 Metagene Link

    HMDB01064 METLIN ID

    5977 PubChem Compound

    5462164 PDB ID

    Not Available ChEBI ID

    15530

    Product: MRT68921 (hydrochloride)

    References Synthesis Reference Kawaguchi, Akihiko; Yoshimura, Tsutomu; Okuda, Shigenobu. A new method for the preparation of acyl-CoA thioesters. Journal of Biochemistry (Tokyo, Japan) (1981), 89(2), 337-9. Material Safety Data Sheet (MSDS) Not Available General References
    1. Ramsay RR, Mancinelli G, Arduini A: Carnitine palmitoyltransferase in human erythrocyte membrane. Properties and malonyl-CoA sensitivity. Biochem J. 1991 May 1;275 ( Pt 3):685-8. [PubMed:2039446 ]
    2. Domergue F, Abbadi A, Ott C, Zank TK, Zahringer U, Heinz E: Acyl carriers used as substrates by the desaturases and elongases involved in very long-chain polyunsaturated fatty acids biosynthesis reconstituted in yeast. J Biol Chem. 2003 Sep 12;278(37):35115-26. Epub 2003 Jun 30. [PubMed:12835316 ]
    3. Kawasaki T, Snyder F: Synthesis of a novel acetylated neutral lipid related to platelet-activating factor by acyl-CoA:1-O-alkyl-2-acetyl-sn-glycerol acyltransferase in HL-60 cells. J Biol Chem. 1988 Feb 25;263(6):2593-6. [PubMed:3422635 ]
    4. Ensenauer R, He M, Willard JM, Goetzman ES, Corydon TJ, Vandahl BB, Mohsen AW, Isaya G, Vockley J: Human acyl-CoA dehydrogenase-9 plays a novel role in the mitochondrial beta-oxidation of unsaturated fatty acids. J Biol Chem. 2005 Sep 16;280(37):32309-16. Epub 2005 Jul 14. [PubMed:16020546 ]
    5. Ciapaite J, Bakker SJ, Van Eikenhorst G, Wagner MJ, Teerlink T, Schalkwijk CG, Fodor M, Ouwens DM, Diamant M, Heine RJ, Westerhoff HV, Krab K: Functioning of oxidative phosphorylation in liver mitochondria of high-fat diet fed rats. Biochim Biophys Acta. 2007 Mar;1772(3):307-16. Epub 2006 Nov 10. [PubMed:17184976 ]
    6. (). Silva C, Loyola G, Valenzuela R, García-Huidobro T, Monasterio O, Bronfman M. High-affinity binding of fatty acyl-CoAs and peroxisome proliferator-CoA esters to glutathione S-transferases effect on enzymatic activity. Eur J Biochem. 1999 Nov;266(1):143-50.. .

    Enzymes

    General function:
    Involved in thiolester hydrolase activity
    Specific function:
    Involved in bile acid metabolism. In liver hepatocytes catalyzes the second step in the conjugation of C24 bile acids (choloneates) to glycine and taurine before excretion into bile canaliculi. The major components of bile are cholic acid and chenodeoxycholic acid. In a first step the bile acids are converted to an acyl-CoA thioester, either in peroxisomes (primary bile acids deriving from the cholesterol pathway), or cytoplasmic at the endoplasmic reticulum (secondary bile acids). May catalyze the conjugation of primary or secondary bile acids, or both. The conjugation increases the detergent properties of bile acids in the intestine, which facilitates lipid and fat-soluble vitamin absorption. In turn, bile acids are deconjugated by bacteria in the intestine and are recycled back to the liver for reconjugation (secondary bile acids). May also act as an acyl-CoA thioesterase that regulates intracellular levels of free fatty acids. In vitro, catalyzes the hydrolysis of long- and very long-chain saturated acyl-CoAs to the free fatty acid and coenzyme A (CoASH), and conjugates glycine to these acyl-CoAs.
    Gene Name:
    BAAT
    Uniprot ID:
    Q14032
    Molecular weight:
    46298.865
    General function:
    Lipid transport and metabolism
    Specific function:
    Acyl-CoA thioesterases are a group of enzymes that catalyze the hydrolysis of acyl-CoAs to the free fatty acid and coenzyme A (CoASH), providing the potential to regulate intracellular levels of acyl-CoAs, free fatty acids and CoASH. May play an important physiological function in brain. May play a regulatory role by modulating the cellular levels of fatty acyl-CoA ligands for certain transcription factors as well as the substrates for fatty acid metabolizing enzymes, contributing to lipid homeostasis. Has broad specificity, active towards fatty acyl-CoAs with chain-lengths of C8-C18. Has a maximal activity toward palmitoyl-CoA.
    Gene Name:
    ACOT7
    Uniprot ID:
    O00154
    Molecular weight:
    40454.945
    Reactions
    Linoleoyl-CoA + Water → Coenzyme A + Linoleic acid details
    General function:
    Involved in thiolester hydrolase activity
    Specific function:
    Acyl-CoA thioesterases are a group of enzymes that catalyze the hydrolysis of acyl-CoAs to the free fatty acid and coenzyme A (CoASH), providing the potential to regulate intracellular levels of acyl-CoAs, free fatty acids and CoASH. Displays high levels of activity on medium- and long chain acyl CoAs.
    Gene Name:
    ACOT2
    Uniprot ID:
    P49753
    Molecular weight:
    53218.02
    Reactions
    Linoleoyl-CoA + Water → Coenzyme A + Linoleic acid details
    General function:
    Involved in thiolester hydrolase activity
    Specific function:
    Acyl-CoA thioesterases are a group of enzymes that catalyze the hydrolysis of acyl-CoAs to the free fatty acid and coenzyme A (CoASH), providing the potential to regulate intracellular levels of acyl-CoAs, free fatty acids and CoASH (By similarity). Succinyl-CoA thioesterase that also hydrolyzes long chain saturated and unsaturated monocarboxylic acyl-CoAs.
    Gene Name:
    ACOT4
    Uniprot ID:
    Q8N9L9
    Molecular weight:
    46326.09
    Reactions
    Linoleoyl-CoA + Water → Coenzyme A + Linoleic acid details
    General function:
    Involved in acyl-CoA thioesterase activity
    Specific function:
    Acyl-CoA thioesterases are a group of enzymes that catalyze the hydrolysis of acyl-CoAs to the free fatty acid and coenzyme A (CoASH), providing the potential to regulate intracellular levels of acyl-CoAs, free fatty acids and CoASH. May mediate Nef-induced down-regulation of CD4. Major thioesterase in peroxisomes. Competes with BAAT (Bile acid CoA: amino acid N-acyltransferase) for bile acid-CoA substrate (such as chenodeoxycholoyl-CoA). Shows a preference for medium-length fatty acyl-CoAs (By similarity). May be involved in the metabolic regulation of peroxisome proliferation.
    Gene Name:
    ACOT8
    Uniprot ID:
    O14734
    Molecular weight:
    35914.02
    General function:
    Involved in acyltransferase activity
    Specific function:
    Acyl-CoA:lysocardiolipin acyltransferase. Possesses both lysophosphatidylinositol acyltransferase (LPIAT) and lysophosphatidylglycerol acyltransferase (LPGAT) activities. Recognizes both monolysocardiolipin and dilysocardiolipin as substrates with a preference for linoleoyl-CoA and oleoyl-CoA as acyl donors. Acts as a remodeling enzyme for cardiolipin, a major membrane polyglycerophospholipid. Converts lysophosphatidic acid (LPA) into phosphatidic acid (PA) with a relatively low activity. Required for establishment of the hematopoietic and endothelial lineages.
    Gene Name:
    LCLAT1
    Uniprot ID:
    Q6UWP7
    Molecular weight:
    44560.815
    General function:
    Involved in thiolester hydrolase activity
    Specific function:
    Acyl-CoA thioesterases are a group of enzymes that catalyze the hydrolysis of acyl-CoAs to the free fatty acid and coenzyme A (CoASH), providing the potential to regulate intracellular levels of acyl-CoAs, free fatty acids and CoASH. Active towards fatty acyl-CoA with chain-lengths of C12-C16 (By similarity).
    Gene Name:
    ACOT1
    Uniprot ID:
    Q86TX2
    Molecular weight:
    46276.96
    Reactions
    Linoleoyl-CoA + Water → Coenzyme A + Linoleic acid details

    PMID: 26395965

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