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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2006-08-13 13:48:23 UTC
Update Date2020-02-26 21:25:01 UTC
HMDB IDHMDB0004185
Secondary Accession Numbers
  • HMDB04185
Metabolite Identification
Common Name5-Hydroxyindoleacetylglycine
Description5-Hydroxyindoleacetylglycine belongs to the class of organic compounds known as n-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 5-Hydroxyindoleacetylglycine exists in all living organisms, ranging from bacteria to humans. 5-Hydroxyindoleacetylglycine has been detected, but not quantified in, a few different foods, such as anatidaes (Anatidae), chickens (Gallus gallus), and domestic pigs (Sus scrofa domestica). This could make 5-hydroxyindoleacetylglycine a potential biomarker for the consumption of these foods. 5-Hydroxyindoleacetylglycine is a primary metabolite. Primary metabolites are metabolically or physiologically essential metabolites. They are directly involved in an organism’s growth, development or reproduction. Based on a literature review a significant number of articles have been published on 5-Hydroxyindoleacetylglycine.
Structure
Data?1582752301
Synonyms
ValueSource
2-[2-(5-Hydroxy-1H-indol-3-yl)acetamido]acetic acidChEBI
5-Hydroxyindoleacetyl glycineChEBI
N-[(5-Hydroxyindol-3-yl)acetyl]-glycineChEBI
2-[2-(5-Hydroxy-1H-indol-3-yl)acetamido]acetateGenerator
5-Hydroxyindole acetylglycineHMDB
Chemical FormulaC12H12N2O4
Average Molecular Weight248.2347
Monoisotopic Molecular Weight248.079706882
IUPAC Name2-[2-(5-hydroxy-1H-indol-3-yl)acetamido]acetic acid
Traditional Name5-hydroxyindoleacetylglycine
CAS Registry NumberNot Available
SMILES
OC(=O)CNC(=O)CC1=CNC2=C1C=C(O)C=C2
InChI Identifier
InChI=1S/C12H12N2O4/c15-8-1-2-10-9(4-8)7(5-13-10)3-11(16)14-6-12(17)18/h1-2,4-5,13,15H,3,6H2,(H,14,16)(H,17,18)
InChI KeyLFUCRBSGQMAKCO-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as n-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
Sub ClassAmino acids, peptides, and analogues
Direct ParentN-acyl-alpha amino acids
Alternative Parents
Substituents
  • N-acyl-alpha-amino acid
  • Hydroxyindole
  • 3-alkylindole
  • Indole
  • Indole or derivatives
  • 1-hydroxy-2-unsubstituted benzenoid
  • Substituted pyrrole
  • Benzenoid
  • Pyrrole
  • Heteroaromatic compound
  • Carboxamide group
  • Secondary carboxylic acid amide
  • Carboxylic acid
  • Monocarboxylic acid or derivatives
  • Azacycle
  • Organoheterocyclic compound
  • Organonitrogen compound
  • Organic oxide
  • Carbonyl group
  • Organopnictogen compound
  • Organic oxygen compound
  • Organooxygen compound
  • Hydrocarbon derivative
  • Organic nitrogen compound
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
RoleNot Available
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogP0.242Not Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.77 g/LALOGPS
logP0.83ALOGPS
logP0.3ChemAxon
logS-2.5ALOGPS
pKa (Strongest Acidic)3.65ChemAxon
pKa (Strongest Basic)-2.8ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count4ChemAxon
Polar Surface Area102.42 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity63.24 m³·mol⁻¹ChemAxon
Polarizability24.15 ųChemAxon
Number of Rings2ChemAxon
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]+157.30631661259
DarkChem[M-H]-152.26331661259
DeepCCS[M+H]+153.64530932474
DeepCCS[M-H]-151.26430932474
DeepCCS[M-2H]-184.38430932474
DeepCCS[M+Na]+159.71530932474
AllCCS[M+H]+154.732859911
AllCCS[M+H-H2O]+151.032859911
AllCCS[M+NH4]+158.132859911
AllCCS[M+Na]+159.132859911
AllCCS[M-H]-156.432859911
AllCCS[M+Na-2H]-156.232859911
AllCCS[M+HCOO]-156.232859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
5-HydroxyindoleacetylglycineOC(=O)CNC(=O)CC1=CNC2=C1C=C(O)C=C24322.2Standard polar33892256
5-HydroxyindoleacetylglycineOC(=O)CNC(=O)CC1=CNC2=C1C=C(O)C=C22260.4Standard non polar33892256
5-HydroxyindoleacetylglycineOC(=O)CNC(=O)CC1=CNC2=C1C=C(O)C=C22920.1Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
5-Hydroxyindoleacetylglycine,1TMS,isomer #1C[Si](C)(C)OC(=O)CNC(=O)CC1=C[NH]C2=CC=C(O)C=C122700.0Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,1TMS,isomer #2C[Si](C)(C)OC1=CC=C2[NH]C=C(CC(=O)NCC(=O)O)C2=C12712.2Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,1TMS,isomer #3C[Si](C)(C)N(CC(=O)O)C(=O)CC1=C[NH]C2=CC=C(O)C=C122685.4Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,1TMS,isomer #4C[Si](C)(C)N1C=C(CC(=O)NCC(=O)O)C2=CC(O)=CC=C212747.5Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,2TMS,isomer #1C[Si](C)(C)OC(=O)CNC(=O)CC1=C[NH]C2=CC=C(O[Si](C)(C)C)C=C122747.7Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,2TMS,isomer #2C[Si](C)(C)OC(=O)CN(C(=O)CC1=C[NH]C2=CC=C(O)C=C12)[Si](C)(C)C2660.9Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,2TMS,isomer #3C[Si](C)(C)OC(=O)CNC(=O)CC1=CN([Si](C)(C)C)C2=CC=C(O)C=C122720.1Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,2TMS,isomer #4C[Si](C)(C)OC1=CC=C2C(=C1)C(CC(=O)NCC(=O)O)=CN2[Si](C)(C)C2768.5Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,2TMS,isomer #5C[Si](C)(C)OC1=CC=C2[NH]C=C(CC(=O)N(CC(=O)O)[Si](C)(C)C)C2=C12678.1Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,2TMS,isomer #6C[Si](C)(C)N(CC(=O)O)C(=O)CC1=CN([Si](C)(C)C)C2=CC=C(O)C=C122705.9Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,3TMS,isomer #1C[Si](C)(C)OC(=O)CN(C(=O)CC1=C[NH]C2=CC=C(O[Si](C)(C)C)C=C12)[Si](C)(C)C2690.1Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,3TMS,isomer #1C[Si](C)(C)OC(=O)CN(C(=O)CC1=C[NH]C2=CC=C(O[Si](C)(C)C)C=C12)[Si](C)(C)C2736.8Standard non polar33892256
5-Hydroxyindoleacetylglycine,3TMS,isomer #1C[Si](C)(C)OC(=O)CN(C(=O)CC1=C[NH]C2=CC=C(O[Si](C)(C)C)C=C12)[Si](C)(C)C2997.8Standard polar33892256
5-Hydroxyindoleacetylglycine,3TMS,isomer #2C[Si](C)(C)OC(=O)CNC(=O)CC1=CN([Si](C)(C)C)C2=CC=C(O[Si](C)(C)C)C=C122746.1Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,3TMS,isomer #2C[Si](C)(C)OC(=O)CNC(=O)CC1=CN([Si](C)(C)C)C2=CC=C(O[Si](C)(C)C)C=C122647.8Standard non polar33892256
5-Hydroxyindoleacetylglycine,3TMS,isomer #2C[Si](C)(C)OC(=O)CNC(=O)CC1=CN([Si](C)(C)C)C2=CC=C(O[Si](C)(C)C)C=C123001.6Standard polar33892256
5-Hydroxyindoleacetylglycine,3TMS,isomer #3C[Si](C)(C)OC(=O)CN(C(=O)CC1=CN([Si](C)(C)C)C2=CC=C(O)C=C12)[Si](C)(C)C2678.8Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,3TMS,isomer #3C[Si](C)(C)OC(=O)CN(C(=O)CC1=CN([Si](C)(C)C)C2=CC=C(O)C=C12)[Si](C)(C)C2790.3Standard non polar33892256
5-Hydroxyindoleacetylglycine,3TMS,isomer #3C[Si](C)(C)OC(=O)CN(C(=O)CC1=CN([Si](C)(C)C)C2=CC=C(O)C=C12)[Si](C)(C)C3033.7Standard polar33892256
5-Hydroxyindoleacetylglycine,3TMS,isomer #4C[Si](C)(C)OC1=CC=C2C(=C1)C(CC(=O)N(CC(=O)O)[Si](C)(C)C)=CN2[Si](C)(C)C2692.7Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,3TMS,isomer #4C[Si](C)(C)OC1=CC=C2C(=C1)C(CC(=O)N(CC(=O)O)[Si](C)(C)C)=CN2[Si](C)(C)C2734.7Standard non polar33892256
5-Hydroxyindoleacetylglycine,3TMS,isomer #4C[Si](C)(C)OC1=CC=C2C(=C1)C(CC(=O)N(CC(=O)O)[Si](C)(C)C)=CN2[Si](C)(C)C3072.0Standard polar33892256
5-Hydroxyindoleacetylglycine,4TMS,isomer #1C[Si](C)(C)OC(=O)CN(C(=O)CC1=CN([Si](C)(C)C)C2=CC=C(O[Si](C)(C)C)C=C12)[Si](C)(C)C2709.5Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,4TMS,isomer #1C[Si](C)(C)OC(=O)CN(C(=O)CC1=CN([Si](C)(C)C)C2=CC=C(O[Si](C)(C)C)C=C12)[Si](C)(C)C2722.9Standard non polar33892256
5-Hydroxyindoleacetylglycine,4TMS,isomer #1C[Si](C)(C)OC(=O)CN(C(=O)CC1=CN([Si](C)(C)C)C2=CC=C(O[Si](C)(C)C)C=C12)[Si](C)(C)C2828.3Standard polar33892256
5-Hydroxyindoleacetylglycine,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CNC(=O)CC1=C[NH]C2=CC=C(O)C=C122992.2Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=CC=C2[NH]C=C(CC(=O)NCC(=O)O)C2=C13006.4Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)N(CC(=O)O)C(=O)CC1=C[NH]C2=CC=C(O)C=C122955.2Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)N1C=C(CC(=O)NCC(=O)O)C2=CC(O)=CC=C212981.5Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CNC(=O)CC1=C[NH]C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C123311.6Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CN(C(=O)CC1=C[NH]C2=CC=C(O)C=C12)[Si](C)(C)C(C)(C)C3187.3Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CNC(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O)C=C123226.8Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)C(CC(=O)NCC(=O)O)=CN2[Si](C)(C)C(C)(C)C3291.3Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC1=CC=C2[NH]C=C(CC(=O)N(CC(=O)O)[Si](C)(C)C(C)(C)C)C2=C13220.8Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)N(CC(=O)O)C(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O)C=C123179.4Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CN(C(=O)CC1=C[NH]C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C12)[Si](C)(C)C(C)(C)C3430.5Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CN(C(=O)CC1=C[NH]C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C12)[Si](C)(C)C(C)(C)C3364.1Standard non polar33892256
5-Hydroxyindoleacetylglycine,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CN(C(=O)CC1=C[NH]C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C12)[Si](C)(C)C(C)(C)C3230.7Standard polar33892256
5-Hydroxyindoleacetylglycine,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CNC(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C123472.4Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CNC(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C123269.8Standard non polar33892256
5-Hydroxyindoleacetylglycine,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CNC(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C123206.7Standard polar33892256
5-Hydroxyindoleacetylglycine,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CN(C(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O)C=C12)[Si](C)(C)C(C)(C)C3364.4Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CN(C(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O)C=C12)[Si](C)(C)C(C)(C)C3369.8Standard non polar33892256
5-Hydroxyindoleacetylglycine,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CN(C(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O)C=C12)[Si](C)(C)C(C)(C)C3222.8Standard polar33892256
5-Hydroxyindoleacetylglycine,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)C(CC(=O)N(CC(=O)O)[Si](C)(C)C(C)(C)C)=CN2[Si](C)(C)C(C)(C)C3429.3Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)C(CC(=O)N(CC(=O)O)[Si](C)(C)C(C)(C)C)=CN2[Si](C)(C)C(C)(C)C3314.8Standard non polar33892256
5-Hydroxyindoleacetylglycine,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)C(CC(=O)N(CC(=O)O)[Si](C)(C)C(C)(C)C)=CN2[Si](C)(C)C(C)(C)C3263.7Standard polar33892256
5-Hydroxyindoleacetylglycine,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CN(C(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C12)[Si](C)(C)C(C)(C)C3579.7Semi standard non polar33892256
5-Hydroxyindoleacetylglycine,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CN(C(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C12)[Si](C)(C)C(C)(C)C3473.6Standard non polar33892256
5-Hydroxyindoleacetylglycine,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CN(C(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C12)[Si](C)(C)C(C)(C)C3156.9Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 5-Hydroxyindoleacetylglycine GC-MS (Non-derivatized) - 70eV, Positivesplash10-00dj-2910000000-8f9961b92d4cc975ff902017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 5-Hydroxyindoleacetylglycine GC-MS (2 TMS) - 70eV, Positivesplash10-00dm-9235000000-11c6442198c07ba85d062017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 5-Hydroxyindoleacetylglycine 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 - 5-Hydroxyindoleacetylglycine 10V, Positive-QTOFsplash10-0002-3390000000-267322535235e15256fe2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5-Hydroxyindoleacetylglycine 20V, Positive-QTOFsplash10-0a6s-9530000000-ed7fc433b7621b5b4cb12017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5-Hydroxyindoleacetylglycine 40V, Positive-QTOFsplash10-0691-5900000000-22519d1552585ade8ea52017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5-Hydroxyindoleacetylglycine 10V, Negative-QTOFsplash10-0002-0090000000-c9c63b6d897b01770e8a2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5-Hydroxyindoleacetylglycine 20V, Negative-QTOFsplash10-006t-4490000000-7e245b831db0a93cc0002017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5-Hydroxyindoleacetylglycine 40V, Negative-QTOFsplash10-05gi-9600000000-4109844798ae0129bc7e2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5-Hydroxyindoleacetylglycine 10V, Positive-QTOFsplash10-006t-0970000000-43e031352772fd99f5eb2021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5-Hydroxyindoleacetylglycine 20V, Positive-QTOFsplash10-0002-0900000000-7c41be203b1014f8e1672021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5-Hydroxyindoleacetylglycine 40V, Positive-QTOFsplash10-000t-0900000000-511a18631f279b1065db2021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5-Hydroxyindoleacetylglycine 10V, Negative-QTOFsplash10-001j-0940000000-9645d51451c00d03a7322021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5-Hydroxyindoleacetylglycine 20V, Negative-QTOFsplash10-001i-1900000000-9e255dc577ae372b9ee62021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5-Hydroxyindoleacetylglycine 40V, Negative-QTOFsplash10-0ac3-9400000000-d45217f4fe448259003b2021-09-25Wishart LabView Spectrum
Biological Properties
Cellular LocationsNot Available
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 IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB023328
KNApSAcK IDNot Available
Chemspider ID389669
KEGG Compound IDC05832
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound440806
PDB IDNot Available
ChEBI ID27631
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available