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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 17:40:55 UTC
Update Date2022-03-07 02:52:49 UTC
HMDB IDHMDB0031094
Secondary Accession Numbers
  • HMDB31094
Metabolite Identification
Common NameGlycerol tributanoate
DescriptionGlycerol tributanoate, also known as butyrin or 1,2,3-tributyrylglycerol, belongs to the class of organic compounds known as triacylglycerols. These are glycerides consisting of three fatty acid chains covalently bonded to a glycerol molecule through ester linkages. Based on a literature review a significant number of articles have been published on Glycerol tributanoate.
Structure
Data?1563862081
Synonyms
ValueSource
1,2,3-Propanetriol, tributyrateChEBI
1,2,3-Propanetriyl tributanoateChEBI
1,2,3-TributanoylglycerolChEBI
1,2,3-TributyrylglycerolChEBI
2,3-Bis(butyryloxy)propyl butyrateChEBI
Butanoic acid, 1,2,3-propanetriyl esterChEBI
ButyrinChEBI
Butyryl triglycerideChEBI
Glycerin tributyrateChEBI
Glycerol tributyrateChEBI
GlyceroltributyrinChEBI
Glyceryl tributyrateChEBI
Propane-1,2,3-triyl tributyrateChEBI
Tri-N-butyrinChEBI
TributinChEBI
Tributyryl glycerideChEBI
1,2,3-Propanetriol, tributyric acidGenerator
1,2,3-Propanetriyl tributanoic acidGenerator
2,3-Bis(butyryloxy)propyl butyric acidGenerator
Butanoate, 1,2,3-propanetriyl esterGenerator
Glycerin tributyric acidGenerator
Glycerol tributyric acidGenerator
Glyceryl tributyric acidGenerator
Propane-1,2,3-triyl tributyric acidGenerator
Glycerol tributanoic acidGenerator
TributyrylglycerolMeSH
Butyric acid triester with glycerinHMDB
FEMA 2223HMDB
KodaflexHMDB
NSC 661583HMDB
Tri-butyrinHMDB
TributyrinHMDB
TributyrinineHMDB
Tributyrl glycerideHMDB
TributyroinHMDB
Glycerol tributanoateChEBI
Chemical FormulaC15H26O6
Average Molecular Weight302.3633
Monoisotopic Molecular Weight302.172938564
IUPAC Name1,3-bis(butanoyloxy)propan-2-yl butanoate
Traditional Nametributyrin
CAS Registry Number60-01-5
SMILES
CCCC(=O)OCC(COC(=O)CCC)OC(=O)CCC
InChI Identifier
InChI=1S/C15H26O6/c1-4-7-13(16)19-10-12(21-15(18)9-6-3)11-20-14(17)8-5-2/h12H,4-11H2,1-3H3
InChI KeyUYXTWWCETRIEDR-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as triacylglycerols. These are glycerides consisting of three fatty acid chains covalently bonded to a glycerol molecule through ester linkages.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassGlycerolipids
Sub ClassTriradylcglycerols
Direct ParentTriacylglycerols
Alternative Parents
Substituents
  • Triacyl-sn-glycerol
  • Tricarboxylic acid or derivatives
  • Fatty acid ester
  • Fatty acyl
  • Carboxylic acid ester
  • Carboxylic acid derivative
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Carbonyl group
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
Ontology
Physiological effect
Disposition
Biological locationRoute of exposureSource
Process
Role
Physical Properties
StateLiquid
Experimental Molecular Properties
PropertyValueReference
Melting Point-75 °CNot Available
Boiling Point189.00 to 190.00 °C. @ 760.00 mm Hg (est)The Good Scents Company Information System
Water Solubility0.13 mg/mL at 37 °CNot Available
LogP4.054 (est)The Good Scents Company Information System
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.32 g/LALOGPS
logP2.71ALOGPS
logP2.92ChemAxon
logS-3ALOGPS
pKa (Strongest Basic)-6.6ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area78.9 ŲChemAxon
Rotatable Bond Count14ChemAxon
Refractivity75.65 m³·mol⁻¹ChemAxon
Polarizability32.97 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+172.0631661259
DarkChem[M-H]-170.40331661259
DeepCCS[M+H]+177.35730932474
DeepCCS[M-H]-174.99930932474
DeepCCS[M-2H]-207.88630932474
DeepCCS[M+Na]+183.45130932474
AllCCS[M+H]+178.032859911
AllCCS[M+H-H2O]+175.432859911
AllCCS[M+NH4]+180.532859911
AllCCS[M+Na]+181.232859911
AllCCS[M-H]-171.332859911
AllCCS[M+Na-2H]-172.232859911
AllCCS[M+HCOO]-173.332859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Glycerol tributanoateCCCC(=O)OCC(COC(=O)CCC)OC(=O)CCC2707.6Standard polar33892256
Glycerol tributanoateCCCC(=O)OCC(COC(=O)CCC)OC(=O)CCC1746.6Standard non polar33892256
Glycerol tributanoateCCCC(=O)OCC(COC(=O)CCC)OC(=O)CCC1931.7Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Experimental GC-MSGC-MS Spectrum - Glycerol tributanoate EI-B (Non-derivatized)splash10-00di-9100000000-a0f9426f5cd5d1ad3c832017-09-12HMDB team, MONA, MassBankView Spectrum
Experimental GC-MSGC-MS Spectrum - Glycerol tributanoate EI-B (Non-derivatized)splash10-00di-9110000000-053a735053ae0621fe882017-09-12HMDB team, MONA, MassBankView Spectrum
Experimental GC-MSGC-MS Spectrum - Glycerol tributanoate EI-B (Non-derivatized)splash10-00di-9100000000-a0f9426f5cd5d1ad3c832018-05-18HMDB team, MONA, MassBankView Spectrum
Experimental GC-MSGC-MS Spectrum - Glycerol tributanoate EI-B (Non-derivatized)splash10-00di-9110000000-053a735053ae0621fe882018-05-18HMDB team, MONA, MassBankView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Glycerol tributanoate GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glycerol tributanoate 10V, Positive-QTOFsplash10-00di-0009000000-c4d130796e01a45caada2017-10-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glycerol tributanoate 20V, Positive-QTOFsplash10-00di-0009000000-c4d130796e01a45caada2017-10-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glycerol tributanoate 40V, Positive-QTOFsplash10-0gb9-0097000000-b93aef222c9f718aa3b22017-10-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glycerol tributanoate 10V, Positive-QTOFsplash10-0a4i-0009000000-38db4a07206d842844152021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glycerol tributanoate 20V, Positive-QTOFsplash10-0a4i-0009000000-38db4a07206d842844152021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glycerol tributanoate 40V, Positive-QTOFsplash10-0ai2-9099000000-12c3d7bdd61a16d085a52021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glycerol tributanoate 10V, Positive-QTOFsplash10-0udi-0459000000-babf77e8c5a51a5e69dd2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glycerol tributanoate 20V, Positive-QTOFsplash10-0v00-2953000000-f878b874e5b39892ae4d2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glycerol tributanoate 40V, Positive-QTOFsplash10-00ds-8900000000-a1b857778d6727f6a47b2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glycerol tributanoate 10V, Positive-QTOFsplash10-00di-0009000000-1e1f8e781385aeed294d2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glycerol tributanoate 20V, Positive-QTOFsplash10-00di-0009000000-1e1f8e781385aeed294d2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glycerol tributanoate 40V, Positive-QTOFsplash10-0gb9-1097000000-9e038df610fe764fc17e2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glycerol tributanoate 10V, Negative-QTOFsplash10-0gw0-9756000000-9862c21f5688e05dd3b02021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glycerol tributanoate 20V, Negative-QTOFsplash10-000i-9800000000-48475bab8381d831aee32021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glycerol tributanoate 40V, Negative-QTOFsplash10-000i-6900000000-acef2739fe3f4e2cd0662021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glycerol tributanoate 10V, Positive-QTOFsplash10-004i-0009000000-ab75fe3f6e5f939e6f272021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glycerol tributanoate 20V, Positive-QTOFsplash10-004i-0009000000-ab75fe3f6e5f939e6f272021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glycerol tributanoate 40V, Positive-QTOFsplash10-004i-0009000000-ab75fe3f6e5f939e6f272021-09-24Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Extracellular
  • Membrane
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDDB12709
Phenol Explorer Compound IDNot Available
FooDB IDFDB003099
KNApSAcK IDNot Available
Chemspider ID13849665
KEGG Compound IDC13870
BioCyc IDCPD-13014
BiGG IDNot Available
Wikipedia LinkButyrin
METLIN IDNot Available
PubChem Compound6050
PDB IDNot Available
ChEBI ID35020
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1595801
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Kobayashi R, Hirano N, Kanaya S, Haruki M: Enhancement of the enzymatic activity of Escherichia coli acetyl esterase by a double mutation obtained by random mutagenesis. Biosci Biotechnol Biochem. 2012;76(11):2082-8. Epub 2012 Nov 7. [PubMed:23132590 ]
  2. Lookene A, Bengtsson-Olivecrona G: Chymotryptic cleavage of lipoprotein lipase. Identification of cleavage sites and functional studies of the truncated molecule. Eur J Biochem. 1993 Apr 1;213(1):185-94. [PubMed:8477692 ]
  3. Biver S, Vandenbol M: Characterization of three new carboxylic ester hydrolases isolated by functional screening of a forest soil metagenomic library. J Ind Microbiol Biotechnol. 2013 Feb;40(2):191-200. doi: 10.1007/s10295-012-1217-7. Epub 2012 Nov 18. [PubMed:23160923 ]
  4. Feng X, Patterson DA, Balaban M, Emanuelsson EA: Enabling the utilization of wool as an enzyme support: enhancing the activity and stability of lipase immobilized onto woolen cloth. Colloids Surf B Biointerfaces. 2013 Feb 1;102:526-33. doi: 10.1016/j.colsurfb.2012.08.037. Epub 2012 Sep 4. [PubMed:23174670 ]
  5. Lesot P, Serhan Z, Aroulanda C, Billault I: Analytical contribution of NAD 2D-NMR spectroscopy in polypeptide mesophases to the investigation of triglycerides. Magn Reson Chem. 2012 Dec;50 Suppl 1:S2-11. doi: 10.1002/mrc.3855. [PubMed:23280656 ]
  6. Heidor R, Ortega JF, de Conti A, Ong TP, Moreno FS: Anticarcinogenic actions of tributyrin, a butyric acid prodrug. Curr Drug Targets. 2012 Dec;13(14):1720-9. [PubMed:23140283 ]
  7. Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
  8. Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
  9. Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
  10. Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
  11. Ghosh S, Strum JC, Bell RM: Lipid biochemistry: functions of glycerolipids and sphingolipids in cellular signaling. FASEB J. 1997 Jan;11(1):45-50. [PubMed:9034165 ]
  12. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
  13. Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.
  14. Linda T. Welson (2006). Triglycerides and Cholesterol Research. Nova Science Publishers Inc..