Showing metabocard for Serinyl-Gamma-glutamate (BMDB0064067)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2020-03-03 19:38:51 UTC
Update Date2020-04-22 15:56:53 UTC
BMDB IDBMDB0064067
Secondary Accession Numbers
  • BMDB64067
Metabolite Identification
Common NameSerinyl-Gamma-glutamate
DescriptionSerinyl-Gamma-glutamate, also known as S-ge dipeptide or serinyl-g-glutamic acid, belongs to the class of organic compounds known as glutamine and derivatives. Glutamine and derivatives are compounds containing glutamine or a derivative thereof resulting from reaction of glutamine 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 very few articles have been published on Serinyl-Gamma-glutamate.
Structure
Thumb
MOLSDF3D-SDFPDBSMILESInChI View 3D Structure
Synonyms
ValueSource
Serinyl-g-glutamateGenerator
Serinyl-g-glutamic acidGenerator
Serinyl-gamma-glutamic acidGenerator
Serinyl-γ-glutamateGenerator
Serinyl-γ-glutamic acidGenerator
L-Serinyl-L-gamma-glutamateHMDB
S-GE dipeptideHMDB
Ser-ggluHMDB
Serine gamma-glutamate dipeptideHMDB
Serine-gamma-glutamate dipeptideHMDB
Serinylgamma-glutamateHMDB
SGE dipeptideHMDB
2-Amino-4-[(2-amino-3-hydroxypropanoyl)-C-hydroxycarbonimidoyl]butanoateHMDB
Chemical FormulaC8H15N3O5
Average Molecular Weight233.2218
Monoisotopic Molecular Weight233.101170605
IUPAC Name2-amino-4-[(2-amino-3-hydroxypropanoyl)carbamoyl]butanoic acid
Traditional Name2-amino-4-[(2-amino-3-hydroxypropanoyl)carbamoyl]butanoic acid
CAS Registry NumberNot Available
SMILES
NC(CCC(=O)NC(=O)C(N)CO)C(O)=O
InChI Identifier
InChI=1S/C8H15N3O5/c9-4(8(15)16)1-2-6(13)11-7(14)5(10)3-12/h4-5,12H,1-3,9-10H2,(H,15,16)(H,11,13,14)
InChI KeyXSBSFWZOXUFADP-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as glutamine and derivatives. Glutamine and derivatives are compounds containing glutamine or a derivative thereof resulting from reaction of glutamine 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 ParentGlutamine and derivatives
Alternative Parents
Substituents
  • Glutamine or derivatives
  • Alpha-amino acid amide
  • Serine or derivatives
  • Alpha-amino acid
  • N-acyl-amine
  • Fatty acid
  • Carboxylic acid imide
  • Dicarboximide
  • Carboxylic acid imide, n-unsubstituted
  • Amino acid
  • Monocarboxylic acid or derivatives
  • Carboxylic acid
  • Primary alcohol
  • Organooxygen compound
  • Organonitrogen compound
  • Hydrocarbon derivative
  • Alcohol
  • Primary aliphatic amine
  • Organic oxide
  • Organopnictogen compound
  • Carbonyl group
  • Amine
  • Organic oxygen compound
  • Organic nitrogen compound
  • Primary amine
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
Ontology
StatusExpected but not Quantified
Origin
  • Endogenous
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-3.4ALOGPS
logP-5.4ChemAxon
logS-1.1ALOGPS
pKa (Strongest Acidic)1.89ChemAxon
pKa (Strongest Basic)9.41ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count7ChemAxon
Hydrogen Donor Count5ChemAxon
Polar Surface Area155.74 ŲChemAxon
Rotatable Bond Count6ChemAxon
Refractivity52.07 m³·mol⁻¹ChemAxon
Polarizability22.19 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Spectra
Spectra
Biological Properties
Cellular LocationsNot Available
Biospecimen LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
HMDB IDHMDB0029053
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB112059
KNApSAcK IDNot Available
Chemspider ID35032824
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound131750784
PDB IDNot Available
ChEBI IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available