Record Information
Version 1.0
Update Date 1/22/2018 11:54:54 AM
Metabolite IDPAMDB100026
Identification
Name: 2-aminobenzoylacetic acid
Description:A 3-oxo monocarboxylic acid that is benzoylacetic acid substituted at position 2 on the benzene ring by an amino group.
Structure
Thumb
Synonyms:Not Available
Chemical Formula: C9H9NO3
Average Molecular Weight: 179.173
Monoisotopic Molecular Weight: 179.058
InChI Key: POAXUNDIOGWQOC-UHFFFAOYSA-N
InChI:InChI=1S/C9H9NO3/c10-7-4-2-1-3-6(7)8(11)5-9(12)13/h1-4H,5,10H2,(H,12,13)
CAS number: Not Available
IUPAC Name:3-(2-aminophenyl)-3-oxopropanoic acid
Traditional IUPAC Name: Not Available
SMILES:C=1(C(=CC=CC1)N)C(CC(O)=O)=O
Chemical Taxonomy
Taxonomy DescriptionThis compound belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group.
Kingdom Organic compounds
Super ClassOrganic oxygen compounds
Class Organooxygen compounds
Sub ClassCarbonyl compounds
Direct Parent Alkyl-phenylketones
Alternative Parents
Substituents
  • Alkyl-phenylketone
  • 3-phenylpropanoic-acid
  • Benzoyl
  • Aryl alkyl ketone
  • Aniline or substituted anilines
  • Beta-keto acid
  • Monocyclic benzene moiety
  • Beta-hydroxy ketone
  • Keto acid
  • 1,3-dicarbonyl compound
  • Benzenoid
  • Vinylogous amide
  • Amino acid
  • Amino acid or derivatives
  • Monocarboxylic acid or derivatives
  • Carboxylic acid
  • Carboxylic acid derivative
  • Primary amine
  • Organic nitrogen compound
  • Organonitrogen compound
  • Organopnictogen compound
  • Hydrocarbon derivative
  • Organic oxide
  • Amine
  • Aromatic homomonocyclic compound
Molecular Framework Aromatic homomonocyclic compounds
External Descriptors Not Available
Physical Properties
State: Not Available
Charge:0
Melting point: Not Available
Experimental Properties: Not Available
Predicted Properties
PropertyValueSource
Mass179.1722ChemAxon
logP1.5074ChemAxon
H-bond acceptors4ChemAxon
H-bond donors2ChemAxon
Rotatable bonds3ChemAxon
PSA80.3900ChemAxon
RO5 violations0ChemAxon
RO3 violations2ChemAxon
Refractivity47.6197ChemAxon
Atoms22ChemAxon
Rings1ChemAxon
Heavy atoms13ChemAxon
Hydrogen atoms9ChemAxon
Heteroatoms4ChemAxon
N/O atoms4ChemAxon
Inorganic atoms0ChemAxon
Halogen atoms0ChemAxon
Chiral centers0ChemAxon
R/S chiral centers0ChemAxon
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:
    • Drees SL, Fetzner S. PqsE of Pseudomonas aeruginosa Acts as Pathway-Specific Thioesterase in the Biosynthesis of Alkylquinolone Signaling Molecules. Chem Biol. 2015 May 21;22(5):611-8. Pubmed: 25960261
    Synthesis Reference: Not Available
    Material Safety Data Sheet (MSDS) Not Available
    External Links: Not Available