Record Information
Version1.0
Creation Date2020-05-06 19:43:18 UTC
Update Date2020-05-07 14:45:15 UTC
BMDB IDBMDB0109714
Secondary Accession NumbersNone
Metabolite Identification
Common Namebeta-Aminoglutaric acid
Descriptionisoglutamic acid, also known as 3-aminoglutarate or isoglutamate, belongs to the class of organic compounds known as amino fatty acids. These are fatty acids containing an amine group. isoglutamic acid is a very strong basic compound (based on its pKa).
Structure
Thumb
Synonyms
ValueSource
3-AminoglutarateChEBI
3-Aminoglutaric acidChEBI
3-Aminopentanedioic acidChEBI
3-Azanylpentanedioic acidChEBI
beta-Aminoglutaric acidChEBI
beta-Glutamic acidChEBI
IsoglutamateKegg
3-AminopentanedioateGenerator
3-AzanylpentanedioateGenerator
b-AminoglutarateGenerator
b-Aminoglutaric acidGenerator
beta-AminoglutarateGenerator
Β-aminoglutarateGenerator
Β-aminoglutaric acidGenerator
b-GlutamateGenerator
b-Glutamic acidGenerator
beta-GlutamateGenerator
Β-glutamateGenerator
Β-glutamic acidGenerator
3-Aminoglutaric acid, sodium saltMeSH
Isoglutamic acidKEGG
Chemical FormulaC5H9NO4
Average Molecular Weight147.1293
Monoisotopic Molecular Weight147.053157781
IUPAC Name3-aminopentanedioic acid
Traditional Nameisoglutamic acid
CAS Registry NumberNot Available
SMILES
NC(CC(O)=O)CC(O)=O
InChI Identifier
InChI=1S/C5H9NO4/c6-3(1-4(7)8)2-5(9)10/h3H,1-2,6H2,(H,7,8)(H,9,10)
InChI KeyBBJIPMIXTXKYLZ-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as amino fatty acids. These are fatty acids containing an amine group.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassFatty Acyls
Sub ClassFatty acids and conjugates
Direct ParentAmino fatty acids
Alternative Parents
Substituents
  • Amino fatty acid
  • Dicarboxylic acid or derivatives
  • Amino acid or derivatives
  • Amino acid
  • Carboxylic acid derivative
  • Carboxylic acid
  • Amine
  • Primary amine
  • Organooxygen compound
  • Organonitrogen compound
  • Primary aliphatic amine
  • Hydrocarbon derivative
  • Organic oxide
  • Organopnictogen compound
  • Carbonyl group
  • Organic oxygen compound
  • Organic nitrogen compound
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
Ontology
StatusDetected but not Quantified
OriginNot Available
BiofunctionNot Available
ApplicationNot Available
Cellular locationsNot Available
Physical Properties
StateNot Available
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP-3.6ALOGPS
logP-3.7ChemAxon
logS-0.21ALOGPS
pKa (Strongest Acidic)3.18ChemAxon
pKa (Strongest Basic)10.64ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count5ChemAxon
Hydrogen Donor Count3ChemAxon
Polar Surface Area100.62 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity31.16 m³·mol⁻¹ChemAxon
Polarizability13.3 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Spectra
SpectraNot Available
Biological Properties
Cellular LocationsNot Available
Biospecimen Locations
  • Liver
  • Mammary Gland
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
LiverDetected but not QuantifiedNot QuantifiedNot SpecifiedNot Specified
Normal
details
Mammary GlandDetected but not QuantifiedNot QuantifiedNot SpecifiedNot Specified
Normal
details
Abnormal Concentrations
Not Available
HMDB IDNot Available
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDC05574
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound73064
PDB IDNot Available
ChEBI ID28791
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available