RefMet Compound Details

Created with Raphaƫl 2.1.0OOHNH2
RefMet ID, RefMet name, exact mass and formula
RefMet IDRM0013238
RefMet name2-Aminobenzoic acid
Systematic name2-aminobenzoic acid
SynonymsPubChem Synonyms
Exact mass137.047679 (neutral)
Calculate m/z:   
View other RefMet entries with this exact (neutral) mass:   +/- 0.05 amu   +/- 0.1 amu   +/- 0.2 amu   +/- 0.5 amu
FormulaC7H7NO2View other entries in RefMet with this formula
Molecular descriptors
Molfile37613 (Download molfile/View MW Metabolite Database details)
InChIInChI=1S/C7H7NO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4H,8H2,(H,9,10)
InChIKeyRWZYAGGXGHYGMB-UHFFFAOYSA-NView other enantiomers/diastereomers of this metabolite in RefMet
SMILESc1ccc(c(c1)C(=O)O)N
Run Tanimoto similarity search (with similarity coefficient >=0.6)
Chemical/Biochemical Classification
Super ClassBenzenoids
Main ClassBenzenes
Sub ClassAminobenzoic acids
Distribution of 2-Aminobenzoic acid in NMDR studies
SpeciesPlot Species distribution
Sample sourcePlot Sample source(tissue) distribution
PlatformPlatform (MS/NMR) used for detection
ChromatographyChromatography methods used for detection
StudiesNMDR Studies reporting 2-Aminobenzoic acid
External Links
Pubchem CID227
ChEBI ID30754
KEGG IDC00108
HMDB IDHMDB0001123
Chemspider ID222
MetaCyc IDANTHRANILATE
EPA CompToxDTXCID7094
Spectral data for 2-Aminobenzoic acid standards
BMRB ID(NMR)View NMR spectra
NP-MRD ID(NMR)View NMR spectra
MassBank(EU)View MS spectra
Structural annotation level
Annotation level1   (1:Known structure; 2:Known regiochemistry; 3:Partial structure; 4:Sum-composition)

Table of KEGG reactions in human pathways involving 2-Aminobenzoic acid

Rxn IDKEGG ReactionEnzyme
R00987 L-Kynurenine + H2O <=> Anthranilate + L-AlanineL-Kynurenine hydrolase
R00988 Formylanthranilate + H2O <=> Formate + AnthranilateN-Formylanthranilate amidohydrolase

Table of KEGG human pathways containing 2-Aminobenzoic acid

Pathway IDHuman Pathway# of reactions
hsa00380 Tryptophan metabolism 2
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