N-(gamma-L-glutamyl)-L-alaninol zwitterion (PAMDB100016)

IdentificationTaxonomyPhysical PropertiesBiological PropertiesSpectraConcentrationsLinksReferencesEnzymes Transporters
Proteins (3280)
Record Information
Version 1.0
Update Date 1/22/2018 11:54:54 AM
Metabolite IDPAMDB100016
Identification
Name: N-(gamma-L-glutamyl)-L-alaninol zwitterion
Description:An amino acid zwitterion obtained by transfer of a proton from the carboxy to the amino group of N-(γ-L-glutamyl)-L-alaninol; major species at pH 7.3.
Structure
Thumb
🔍MOLSDFPDBSMILESInChIView Structure
Synonyms:
  • γ-glutamyl-L-alaninol
Chemical Formula: C8H16N2O4
Average Molecular Weight: 204.2236
Monoisotopic Molecular Weight: 204.111
InChI Key: JJWXGBABENFUNJ-WDSKDSINSA-N
InChI:InChI=1S/C8H16N2O4/c1-5(4-11)10-7(12)3-2-6(9)8(13)14/h5-6,11H,2-4,9H2,1H3,(H,10,12)(H,13,14)/t5-,6-/m0/s1
CAS number: Not Available
IUPAC Name:(2S)-2-azaniumyl-5-{[(2S)-1-hydroxypropan-2-yl]amino}-5-oxopentanoate
Traditional IUPAC Name: Not Available
SMILES:C[C@@H](CO)NC(=O)CC[C@H]([NH3+])C([O-])=O
Chemical Taxonomy
Taxonomy DescriptionThis compound belongs to the class of organic compounds known as glutamine and derivatives. These 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.
Kingdom Organic compounds
Super ClassOrganic acids and derivatives
Class Carboxylic acids and derivatives
Sub ClassAmino acids, peptides, and analogues
Direct Parent Glutamine and derivatives
Alternative Parents
Substituents
  • Glutamine or derivatives
  • Alpha-amino acid
  • L-alpha-amino acid
  • Fatty amide
  • N-acyl-amine
  • Fatty acyl
  • Fatty acid
  • Carboxamide group
  • Carboxylic acid salt
  • Amino acid
  • Secondary carboxylic acid amide
  • Carboxylic acid
  • Monocarboxylic acid or derivatives
  • Primary amine
  • Primary alcohol
  • Organooxygen compound
  • Organonitrogen compound
  • Hydrocarbon derivative
  • Primary aliphatic amine
  • Organic oxide
  • Alcohol
  • Organopnictogen compound
  • Organic oxygen compound
  • Carbonyl group
  • Amine
  • Organic nitrogen compound
  • Organic salt
  • Organic zwitterion
  • Aliphatic acyclic compound
Molecular Framework Aliphatic acyclic compounds
External Descriptors
  • N(5)-alkyl-L-glutamine (CHEBI:85894)
Physical Properties
State: Not Available
Charge:0
Melting point: Not Available
Experimental Properties: Not Available
Predicted Properties
PropertyValueSource
Mass204.2237ChemAxon
logP-2.9851ChemAxon
H-bond acceptors6ChemAxon
H-bond donors3ChemAxon
Rotatable bonds7ChemAxon
PSA117.1000ChemAxon
RO5 violations0ChemAxon
RO3 violations3ChemAxon
Refractivity48.5281ChemAxon
Atoms30ChemAxon
Rings0ChemAxon
Heavy atoms14ChemAxon
Hydrogen atoms16ChemAxon
Heteroatoms6ChemAxon
N/O atoms6ChemAxon
Inorganic atoms0ChemAxon
Halogen atoms0ChemAxon
Chiral centers2ChemAxon
R/S chiral centers2ChemAxon
Unknown chiral centers0ChemAxon
Undefined chiral centers0ChemAxon
Stereo double bonds0ChemAxon
Cis/trans stereo double bonds0ChemAxon
Unknown stereo double bonds0ChemAxon
Undefined stereo double bonds 0ChemAxon
Biological Properties
Cellular Locations: Not Available
Reactions:
Pathways:
    Spectra
    Spectra: Not Available
    References
    References:
    • de Azevedo Wäsch SI, van der Ploeg JR, Maire T, Lebreton A, Kiener A, Leisinger T. Transformation of isopropylamine to L-alaninol by Pseudomonas sp. strain KIE171 involves N-glutamylated intermediates. Appl Environ Microbiol. 2002 May;68(5):2368-75. Pubmed: 11976110
    Synthesis Reference: Not Available
    Material Safety Data Sheet (MSDS) Not Available
    External Links:
    ResourceLink
    MetaCycCPD-9373