Record Information
Version1.0
Creation Date2020-03-03 19:23:58 UTC
Update Date2020-04-22 15:55:16 UTC
BMDB IDBMDB0063811
Secondary Accession Numbers
  • BMDB63811
Metabolite Identification
Common NameAspartyl-Aspartate
DescriptionAspartyl-Aspartate, also known as D-D dipeptide or asp-asp, belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond. Based on a literature review a significant number of articles have been published on Aspartyl-Aspartate.
Structure
Thumb
Synonyms
ValueSource
Aspartyl-aspartic acidGenerator
Asp-aspHMDB
Aspartate aspartate dipeptideHMDB
Aspartate-aspartate dipeptideHMDB
AspartylaspartateHMDB
D-D DipeptideHMDB
DD DipeptideHMDB
L-Aspartyl-L-aspartateHMDB
2-[(2-Amino-3-carboxy-1-hydroxypropylidene)amino]butanedioateHMDB
Chemical FormulaC8H12N2O7
Average Molecular Weight248.1901
Monoisotopic Molecular Weight248.064450748
IUPAC Name2-(2-amino-3-carboxypropanamido)butanedioic acid
Traditional Name2-(2-amino-3-carboxypropanamido)butanedioic acid
CAS Registry NumberNot Available
SMILES
NC(CC(O)=O)C(=O)NC(CC(O)=O)C(O)=O
InChI Identifier
InChI=1S/C8H12N2O7/c9-3(1-5(11)12)7(15)10-4(8(16)17)2-6(13)14/h3-4H,1-2,9H2,(H,10,15)(H,11,12)(H,13,14)(H,16,17)
InChI KeyFRYULLIZUDQONW-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
Sub ClassAmino acids, peptides, and analogues
Direct ParentDipeptides
Alternative Parents
Substituents
  • Alpha-dipeptide
  • Aspartic acid or derivatives
  • Acyl-homoserine
  • N-acyl-alpha-amino acid
  • N-acyl-alpha amino acid or derivatives
  • Alpha-amino acid amide
  • Alpha-amino acid or derivatives
  • Tricarboxylic acid or derivatives
  • Fatty amide
  • Fatty acyl
  • N-acyl-amine
  • Amino acid or derivatives
  • Carboxamide group
  • Amino acid
  • Secondary carboxylic acid amide
  • Carboxylic acid
  • Organooxygen compound
  • Primary amine
  • Primary aliphatic amine
  • Hydrocarbon derivative
  • Organic oxide
  • Carbonyl group
  • Organopnictogen compound
  • Amine
  • Organic oxygen compound
  • Organic nitrogen compound
  • Organonitrogen compound
  • 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-3.3ALOGPS
logP-4.9ChemAxon
logS-1.4ALOGPS
pKa (Strongest Acidic)2.79ChemAxon
pKa (Strongest Basic)8.53ChemAxon
Physiological Charge-2ChemAxon
Hydrogen Acceptor Count8ChemAxon
Hydrogen Donor Count5ChemAxon
Polar Surface Area167.02 ŲChemAxon
Rotatable Bond Count7ChemAxon
Refractivity49.87 m³·mol⁻¹ChemAxon
Polarizability21.48 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 IDHMDB0028749
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB111804
KNApSAcK IDNot Available
Chemspider ID295009
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound332965
PDB IDNot Available
ChEBI ID174279
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available