Metabolomics Structure Database

 
MW REGNO: 37817
Common Name:3-Hydroxyanthranilic acid
Systematic Name:2-amino-3-hydroxybenzoic acid
RefMet Name:3-Hydroxyanthranilic acid
Synonyms: [PubChem Synonyms]
Exact Mass:
153.0426 (neutral)    Calculate m/z:
Formula:C7H7NO3
InChIKey:WJXSWCUQABXPFS-UHFFFAOYSA-N
ClassyFire superclass:Benzenoids [C0002448]
ClassyFire class:Benzene and substituted derivatives [C0002279]
ClassyFire subclass:Benzoic acids and derivatives [C0000176]
ClassyFire direct parent:Hydroxybenzoic acid derivatives [C0001248]
Massbank MS spectra:View MS spectra
NP-MRD NMR spectra:View NMR spectra
SMILES:c1cc(c(c(c1)O)N)C(=O)O
Studies:Available studies (via RefMet name)

Select appropriate tab below to view additional details:

External database links:

PubChem CID:86
CHEBI ID:15793
HMDB ID:HMDB0001476
KEGG ID:C00632
Chemspider ID:84
METLIN ID:3275
BMRB ID:bmse000321
MetaCyc ID:3-HYDROXY-ANTHRANILATE
NP-MRD ID(NMR):NP0000205
Plant Metabolite Hub(Pmhub):MS000000175

Calculated physicochemical properties (?):

Heavy Atoms: 11  
Rings: 1  
Aromatic Rings: 1  
Rotatable Bonds: 1  
van der Waals Molecular volume: 133.21 Å3 molecule-1  
Toplogical Polar Sufrace Area: 83.55 Å2 molecule-1  
Hydrogen Bond Donors: 3  
Hydrogen Bond Acceptors: 3  
logP: 0.67  
Molar Refractivity: 39.48  
Fraction sp3 Carbons: 0.00  
sp3 Carbons: 0  

Human Pathway links:

HMDB and KEGG pathways containing this metabolite

REACTOME pathways containing this metabolite

References

LIPID MAPS classification: "Update of the LIPID MAPS comprehensive classification system for lipids", Fahy E, Subramaniam S, Murphy RC, Nishijima M, Raetz CR, Shimizu T, Spener F, van Meer G, Wakelam MJ, and Dennis EA, J. Lipid Res. (2009) 50: S9-S14. DOI: 10.1194/jlr.R800095-JLR200
ClassyFire classification: "ClassyFire: automated chemical classification with a comprehensive, computable taxonomy", Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS, J. Cheminformatics (2016) 8:61. DOI: 10.1186/s13321-016-0174-y

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