Showing metabocard for Gamma Glutamylglutamic acid (BMDB0011737)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2016-10-03 18:23:46 UTC
Update Date2020-05-05 18:38:31 UTC
BMDB IDBMDB0011737
Secondary Accession Numbers
  • BMDB11737
Metabolite Identification
Common NameGamma Glutamylglutamic acid
Descriptiongamma-Glutamylglutamic acid, also known as g-glutamylglutamate or gamma-L-glu-L-glu, 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. Based on a literature review a small amount of articles have been published on gamma-Glutamylglutamic acid.
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
(5-L-Glutamyl)-L-glutamateChEBI
gamma-GlutamylglutamateChEBI
gamma-L-Glu-L-gluChEBI
(5-L-Glutamyl)-L-glutamic acidGenerator
g-GlutamylglutamateGenerator
g-Glutamylglutamic acidGenerator
Γ-glutamylglutamateGenerator
Γ-glutamylglutamic acidGenerator
g-L-Glu-L-gluGenerator
Γ-L-glu-L-gluGenerator
γ-Glu-GluHMDB, Generator
γ-L-Glutamyl-L-glutamic acidHMDB
γ-L-Glutamyl-L-glutamateHMDB
L-γ-Glutamyl-L-glutamic acidHMDB
L-γ-Glutamyl-L-glutamateHMDB
N-γ-Glutamylglutamic acidHMDB
N-γ-GlutamylglutamateHMDB
N-L-γ-Glutamylglutamic acidHMDB
N-L-γ-GlutamylglutamateHMDB
N-L-γ-Glutamyl-L-glutamic acidHMDB
N-L-γ-Glutamyl-L-glutamateHMDB
gamma-Glu-GluHMDB
gamma-L-Glutamyl-L-glutamic acidHMDB
gamma-L-Glutamyl-L-glutamateHMDB, MeSH
L-gamma-Glutamyl-L-glutamic acidHMDB
L-gamma-Glutamyl-L-glutamateHMDB
N-gamma-Glutamylglutamic acidHMDB
N-gamma-GlutamylglutamateHMDB
N-L-gamma-Glutamylglutamic acidHMDB
N-L-gamma-GlutamylglutamateHMDB
N-L-gamma-Glutamyl-L-glutamic acidHMDB
N-L-gamma-Glutamyl-L-glutamateHMDB
gamma-Glutamylglutamic acidHMDB, Generator
N-gamma-L-Glutamyl-L-glutamic acidHMDB
N-γ-L-Glutamyl-L-glutamic acidHMDB
N-γ-L-Glutamyl-L-glutamateHMDB
N-gamma-L-Glutamyl-L-glutamateHMDB
g-Glu-GluGenerator, HMDB
Chemical FormulaC10H16N2O7
Average Molecular Weight276.2432
Monoisotopic Molecular Weight276.095750876
IUPAC Name(2S)-2-[(4S)-4-amino-4-carboxybutanamido]pentanedioic acid
Traditional Name(2S)-2-[(4S)-4-amino-4-carboxybutanamido]pentanedioic acid
CAS Registry Number1116-22-9
SMILES
N[C@@H](CCC(=O)N[C@@H](CCC(O)=O)C(O)=O)C(O)=O
InChI Identifier
InChI=1S/C10H16N2O7/c11-5(9(16)17)1-3-7(13)12-6(10(18)19)2-4-8(14)15/h5-6H,1-4,11H2,(H,12,13)(H,14,15)(H,16,17)(H,18,19)/t5-,6-/m0/s1
InChI KeyOWQDWQKWSLFFFR-WDSKDSINSA-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-alpha amino acid or derivatives
  • Alpha-amino acid
  • L-alpha-amino acid
  • Tricarboxylic acid or derivatives
  • Amino acid
  • Carboximidic acid
  • Carboximidic acid derivative
  • Carboxylic acid
  • Propargyl-type 1,3-dipolar organic compound
  • Organic 1,3-dipolar compound
  • Organooxygen compound
  • Organonitrogen compound
  • Organopnictogen compound
  • Organic oxygen compound
  • Primary aliphatic amine
  • Amine
  • Organic nitrogen compound
  • Primary amine
  • Organic oxide
  • Carbonyl group
  • Hydrocarbon derivative
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
Ontology
StatusDetected but not Quantified
Origin
  • Endogenous
BiofunctionNot Available
ApplicationNot Available
Cellular locationsNot Available
Physical Properties
StateSolid
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP-3.2ALOGPS
logP-4.2ChemAxon
logS-1.6ALOGPS
pKa (Strongest Acidic)1.93ChemAxon
pKa (Strongest Basic)9.31ChemAxon
Physiological Charge-2ChemAxon
Hydrogen Acceptor Count8ChemAxon
Hydrogen Donor Count5ChemAxon
Polar Surface Area167.02 ŲChemAxon
Rotatable Bond Count9ChemAxon
Refractivity59.38 m³·mol⁻¹ChemAxon
Polarizability25.7 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Spectra
Spectra
Biological Properties
Cellular LocationsNot Available
Biospecimen Locations
  • Liver
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
LiverDetected but not QuantifiedNot QuantifiedNot SpecifiedNot Specified
Normal		 details
Abnormal Concentrations
Not Available
HMDB IDHMDB0011737
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB028415
KNApSAcK IDNot Available
Chemspider ID83831
KEGG Compound IDC05282
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound92865
PDB IDNot Available
ChEBI ID73705
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available