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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 23:59:50 UTC
Update Date2021-10-13 07:15:02 UTC
HMDB IDHMDB0038665
Secondary Accession Numbers
  • HMDB38665
Metabolite Identification
Common NameIndole-3-acetylglutamic acid
DescriptionIndole-3-acetylglutamic acid belongs to the class of organic compounds known as glutamic acid and derivatives. Glutamic acid and derivatives are compounds containing glutamic acid or a derivative thereof resulting from the reaction of glutamic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. Indole-3-acetylglutamic acid is an extremely weak basic (essentially neutral) compound (based on its pKa). Indole-3-acetylglutamic acid is a constituent of various plant species including soybean (Glycine max) and pulses.
Structure
Data?1583942076
Synonyms
ValueSource
Indole-3-acetylglutamateGenerator
Indoleacetyl glutamateHMDB
IAA-gluHMDB
Indole-3-acetyl glutamateHMDB
Indole-3-acetyl-gluHMDB
Indole-3-acetyl-glutamic acidHMDB
L-N-(1H-indol-3-Ylacetyl)glutamic acidHMDB
N-(Indole-3-acetyl)glutamic acidHMDB
N-[2-(1H-indol-3-yl)Acetyl]-L-glutamic acidHMDB
Indole-3-acetylglutamic acidHMDB
Chemical FormulaC15H16N2O5
Average Molecular Weight304.302
Monoisotopic Molecular Weight304.105921623
IUPAC Name(2S)-2-{[1-hydroxy-2-(1H-indol-3-yl)ethylidene]amino}pentanedioic acid
Traditional Name(2S)-2-{[1-hydroxy-2-(1H-indol-3-yl)ethylidene]amino}pentanedioic acid
CAS Registry Number57105-48-3
SMILES
OC(=O)CC[C@H](NC(=O)CC1=CNC2=C1C=CC=C2)C(O)=O
InChI Identifier
InChI=1S/C15H16N2O5/c18-13(17-12(15(21)22)5-6-14(19)20)7-9-8-16-11-4-2-1-3-10(9)11/h1-4,8,12,16H,5-7H2,(H,17,18)(H,19,20)(H,21,22)/t12-/m0/s1
InChI KeyYRKLGWOHYXIKSF-LBPRGKRZSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as glutamic acid and derivatives. Glutamic acid and derivatives are compounds containing glutamic acid or a derivative thereof resulting from reaction of glutamic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
Sub ClassAmino acids, peptides, and analogues
Direct ParentGlutamic acid and derivatives
Alternative Parents
Substituents
  • Glutamic acid or derivatives
  • N-acyl-alpha-amino acid
  • N-acyl-l-alpha-amino acid
  • N-acyl-alpha amino acid or derivatives
  • 3-alkylindole
  • Indole
  • Indole or derivatives
  • Dicarboxylic acid or derivatives
  • Substituted pyrrole
  • Benzenoid
  • Heteroaromatic compound
  • Pyrrole
  • Secondary carboxylic acid amide
  • Carboxamide group
  • Carboxylic acid
  • Azacycle
  • Organoheterocyclic compound
  • Carbonyl group
  • Organooxygen compound
  • Organonitrogen compound
  • Hydrocarbon derivative
  • Organic oxide
  • Organic oxygen compound
  • Organic nitrogen compound
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Disposition

Biological location

Source

Route of exposure

Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point162.5 °CNot Available
Boiling PointNot AvailableNot Available
Water Solubility300.4 mg/L @ 25 °C (est)The Good Scents Company Information System
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.19 g/LALOGPS
logP10(1.04) g/LALOGPS
logP10(1.64) g/LChemAxon
logS10(-3.4) g/LALOGPS
pKa (Strongest Acidic)3.67ChemAxon
pKa (Strongest Basic)1.19ChemAxon
Physiological Charge-2ChemAxon
Hydrogen Acceptor Count6ChemAxon
Hydrogen Donor Count4ChemAxon
Polar Surface Area122.98 ŲChemAxon
Rotatable Bond Count7ChemAxon
Refractivity77.06 m³·mol⁻¹ChemAxon
Polarizability29.75 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Indole-3-acetylglutamic acidOC(=O)CC[C@H](NC(=O)CC1=CNC2=C1C=CC=C2)C(O)=O4371.5Standard polar33892256
Indole-3-acetylglutamic acidOC(=O)CC[C@H](NC(=O)CC1=CNC2=C1C=CC=C2)C(O)=O2429.4Standard non polar33892256
Indole-3-acetylglutamic acidOC(=O)CC[C@H](NC(=O)CC1=CNC2=C1C=CC=C2)C(O)=O3046.3Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Indole-3-acetylglutamic acid,1TMS,isomer #1C[Si](C)(C)OC(=O)CC[C@H](NC(=O)CC1=C[NH]C2=CC=CC=C12)C(=O)O2995.4Semi standard non polar33892256
Indole-3-acetylglutamic acid,1TMS,isomer #2C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)CC1=C[NH]C2=CC=CC=C122981.9Semi standard non polar33892256
Indole-3-acetylglutamic acid,1TMS,isomer #3C[Si](C)(C)N(C(=O)CC1=C[NH]C2=CC=CC=C12)[C@@H](CCC(=O)O)C(=O)O2989.4Semi standard non polar33892256
Indole-3-acetylglutamic acid,1TMS,isomer #4C[Si](C)(C)N1C=C(CC(=O)N[C@@H](CCC(=O)O)C(=O)O)C2=CC=CC=C213022.1Semi standard non polar33892256
Indole-3-acetylglutamic acid,2TMS,isomer #1C[Si](C)(C)OC(=O)CC[C@H](NC(=O)CC1=C[NH]C2=CC=CC=C12)C(=O)O[Si](C)(C)C2967.4Semi standard non polar33892256
Indole-3-acetylglutamic acid,2TMS,isomer #2C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C2954.5Semi standard non polar33892256
Indole-3-acetylglutamic acid,2TMS,isomer #3C[Si](C)(C)OC(=O)CC[C@H](NC(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)O2983.9Semi standard non polar33892256
Indole-3-acetylglutamic acid,2TMS,isomer #4C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C2960.9Semi standard non polar33892256
Indole-3-acetylglutamic acid,2TMS,isomer #5C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C122978.2Semi standard non polar33892256
Indole-3-acetylglutamic acid,2TMS,isomer #6C[Si](C)(C)N(C(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)[C@@H](CCC(=O)O)C(=O)O2941.8Semi standard non polar33892256
Indole-3-acetylglutamic acid,3TMS,isomer #1C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C2976.9Semi standard non polar33892256
Indole-3-acetylglutamic acid,3TMS,isomer #1C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C2880.5Standard non polar33892256
Indole-3-acetylglutamic acid,3TMS,isomer #2C[Si](C)(C)OC(=O)CC[C@H](NC(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)O[Si](C)(C)C2964.7Semi standard non polar33892256
Indole-3-acetylglutamic acid,3TMS,isomer #2C[Si](C)(C)OC(=O)CC[C@H](NC(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)O[Si](C)(C)C2813.4Standard non polar33892256
Indole-3-acetylglutamic acid,3TMS,isomer #3C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)[Si](C)(C)C2922.8Semi standard non polar33892256
Indole-3-acetylglutamic acid,3TMS,isomer #3C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)[Si](C)(C)C2902.7Standard non polar33892256
Indole-3-acetylglutamic acid,3TMS,isomer #4C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)[Si](C)(C)C2957.0Semi standard non polar33892256
Indole-3-acetylglutamic acid,3TMS,isomer #4C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)[Si](C)(C)C2869.6Standard non polar33892256
Indole-3-acetylglutamic acid,4TMS,isomer #1C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)[Si](C)(C)C2961.9Semi standard non polar33892256
Indole-3-acetylglutamic acid,4TMS,isomer #1C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)[Si](C)(C)C2870.8Standard non polar33892256
Indole-3-acetylglutamic acid,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)CC1=C[NH]C2=CC=CC=C12)C(=O)O3285.8Semi standard non polar33892256
Indole-3-acetylglutamic acid,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)CC1=C[NH]C2=CC=CC=C123265.6Semi standard non polar33892256
Indole-3-acetylglutamic acid,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)N(C(=O)CC1=C[NH]C2=CC=CC=C12)[C@@H](CCC(=O)O)C(=O)O3243.2Semi standard non polar33892256
Indole-3-acetylglutamic acid,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)N1C=C(CC(=O)N[C@@H](CCC(=O)O)C(=O)O)C2=CC=CC=C213251.3Semi standard non polar33892256
Indole-3-acetylglutamic acid,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)CC1=C[NH]C2=CC=CC=C12)C(=O)O[Si](C)(C)C(C)(C)C3491.3Semi standard non polar33892256
Indole-3-acetylglutamic acid,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C(C)(C)C3484.5Semi standard non polar33892256
Indole-3-acetylglutamic acid,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)O3459.5Semi standard non polar33892256
Indole-3-acetylglutamic acid,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C(C)(C)C3471.1Semi standard non polar33892256
Indole-3-acetylglutamic acid,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C123447.1Semi standard non polar33892256
Indole-3-acetylglutamic acid,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)N(C(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)[C@@H](CCC(=O)O)C(=O)O3419.9Semi standard non polar33892256
Indole-3-acetylglutamic acid,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C(C)(C)C3679.1Semi standard non polar33892256
Indole-3-acetylglutamic acid,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C(C)(C)C3447.1Standard non polar33892256
Indole-3-acetylglutamic acid,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)O[Si](C)(C)C(C)(C)C3580.3Semi standard non polar33892256
Indole-3-acetylglutamic acid,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)O[Si](C)(C)C(C)(C)C3370.2Standard non polar33892256
Indole-3-acetylglutamic acid,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)[Si](C)(C)C(C)(C)C3608.6Semi standard non polar33892256
Indole-3-acetylglutamic acid,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)[Si](C)(C)C(C)(C)C3426.8Standard non polar33892256
Indole-3-acetylglutamic acid,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)[Si](C)(C)C(C)(C)C3609.6Semi standard non polar33892256
Indole-3-acetylglutamic acid,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)[Si](C)(C)C(C)(C)C3399.5Standard non polar33892256
Indole-3-acetylglutamic acid,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)[Si](C)(C)C(C)(C)C3754.8Semi standard non polar33892256
Indole-3-acetylglutamic acid,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)[Si](C)(C)C(C)(C)C3559.8Standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Indole-3-acetylglutamic acid GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Experimental LC-MS/MSLC-MS/MS Spectrum - Indole-3-acetylglutamic acid LC-ESI-QTOF 10V, positive-QTOFsplash10-001i-0901000000-c38a8052c2b069a5f7fc2020-07-21HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Indole-3-acetylglutamic acid LC-ESI-QTOF 30V, positive-QTOFsplash10-001i-0900000000-f89084068ea0b8530e302020-07-21HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Indole-3-acetylglutamic acid LC-ESI-QTOF 50V, positive-QTOFsplash10-001i-0900000000-11cd3337a190b43b95132020-07-21HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Indole-3-acetylglutamic acid 10V, Positive-QTOFsplash10-0a4i-0419000000-4c565cd4880c4dfa1ab32021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Indole-3-acetylglutamic acid 10V, Positive-QTOFsplash10-001i-0901000000-4ec54d32aa860fc16a8c2021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Indole-3-acetylglutamic acid 6V, Positive-QTOFsplash10-0a4i-0519000000-2e141c602b5552d1d1712021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Indole-3-acetylglutamic acid 6V, Positive-QTOFsplash10-001i-0901000000-957cf97cd2fc86ba46fa2021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Indole-3-acetylglutamic acid 6V, Positive-QTOFsplash10-001i-0900000000-518ec0c0eb49bfb14bd12021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Indole-3-acetylglutamic acid 10V, Positive-QTOFsplash10-001i-0901000000-c5434dd0f658b9da96382021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Indole-3-acetylglutamic acid 30V, Positive-QTOFsplash10-001i-0900000000-b71effdb282a2722e47c2021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Indole-3-acetylglutamic acid 50V, Positive-QTOFsplash10-001i-0900000000-8bbdc99f808cf1e4990d2021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Indole-3-acetylglutamic acid 10V, Positive-QTOFsplash10-0a4i-0619000000-a40b2cf6d0d71d0c0ca82021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Indole-3-acetylglutamic acid 50V, Positive-QTOFsplash10-001i-0900000000-3017ad85b3ab640f57b02021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Indole-3-acetylglutamic acid 6V, Positive-QTOFsplash10-001i-0901000000-530696548ce11b92f81a2021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Indole-3-acetylglutamic acid 30V, Positive-QTOFsplash10-001i-0900000000-86ccfb443f396ec3bc9e2021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Indole-3-acetylglutamic acid 30V, Positive-QTOFsplash10-001i-0900000000-8d794b5818bf383877012021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Indole-3-acetylglutamic acid 6V, Positive-QTOFsplash10-001i-0900000000-ffb55bc04bc3f74807392021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Indole-3-acetylglutamic acid 50V, Positive-QTOFsplash10-001i-0900000000-ab089d60455f19290f802021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Indole-3-acetylglutamic acid 10V, Positive-QTOFsplash10-0a4i-0519000000-e3978748e96b65a19b8e2021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Indole-3-acetylglutamic acid 10V, Positive-QTOFsplash10-001i-0901000000-53cb9c184a6b28cccfb62021-09-20HMDB team, MONAView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Indole-3-acetylglutamic acid 10V, Positive-QTOFsplash10-0a4i-0954000000-e353414100b60f7627802021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Indole-3-acetylglutamic acid 20V, Positive-QTOFsplash10-053r-0910000000-f56ab928b534215da4ae2021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Indole-3-acetylglutamic acid 40V, Positive-QTOFsplash10-001i-0900000000-978930dad6a07387da482021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Indole-3-acetylglutamic acid 10V, Negative-QTOFsplash10-0f96-1931000000-6d2e52e90a49d39a79812021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Indole-3-acetylglutamic acid 20V, Negative-QTOFsplash10-0f6x-4920000000-2e6cf0ae290d9a0ebf202021-09-25Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm
  • Extracellular
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 IDFDB112397
KNApSAcK IDNot Available
Chemspider ID5445900
KEGG Compound IDNot Available
BioCyc IDINDOLE-3-ACETYL-GLU
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound7097227
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1743401
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .