Metabolomics Structure Database

 
MW REGNO: 37183
Common Name:Uric acid
Systematic Name:2,3,6,7,8,9-hexahydro-1H-purine-2,6,8-trione
RefMet Name:Uric acid
Synonyms: [PubChem Synonyms]
Exact Mass:
168.0283 (neutral)    Calculate m/z:
Formula:C5H4N4O3
InChIKey:LEHOTFFKMJEONL-UHFFFAOYSA-N
ClassyFire superclass:Organoheterocyclic compounds [C0000002]
ClassyFire class:Imidazopyrimidines [C0001797]
ClassyFire subclass:Purines and purine derivatives [C0000245]
ClassyFire direct parent:Xanthines [C0000247]
MoNA MS spectra:View MS spectra
NP-MRD NMR spectra:View NMR spectra
SMILES:c12c([nH]c(=O)[nH]2)[nH]c(=O)[nH]c1=O
Studies:Available studies (via RefMet name)

Select appropriate tab below to view additional details:

External database links:

PubChem CID:1175
CHEBI ID:17775
HMDB ID:HMDB0000289
KEGG ID:C00366
Chemspider ID:1142
METLIN ID:88
BMRB ID:bmse000126
MetaCyc ID:URATE
NP-MRD ID(NMR):NP0001495
EPA CompTox DB:DTXCID60197182
Plant Metabolite Hub(Pmhub):MS000000609

Calculated physicochemical properties (?):

Heavy Atoms: 12  
Rings: 2  
Aromatic Rings: 2  
Rotatable Bonds: 0  
van der Waals Molecular volume: 108.35 Å3 molecule-1  
Toplogical Polar Sufrace Area: 114.37 Å2 molecule-1  
Hydrogen Bond Donors: 4  
Hydrogen Bond Acceptors: 3  
logP: 0.31  
Molar Refractivity: 40.21  
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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