Metabolomics Structure Database

 
MW REGNO: 37135
Common Name:Oxoglutaric acid
Systematic Name:2-oxopentanedioic acid
RefMet Name:2-Oxoglutaric acid
Synonyms:alpha-ketoglutaric acid; alpha-ketoglutarate; Oxoglutarate [PubChem Synonyms]
Exact Mass:
146.0215 (neutral)    Calculate m/z:
Formula:C5H6O5
InChIKey:KPGXRSRHYNQIFN-UHFFFAOYSA-N
ClassyFire superclass:Organic acids and derivatives [C0000264]
ClassyFire class:Keto acids and derivatives [C0000389]
ClassyFire subclass:Gamma-keto acids and derivatives [C0001115]
ClassyFire direct parent:Gamma-keto acids and derivatives [C0001115]
MoNA MS spectra:View MS spectra
NP-MRD NMR spectra:View NMR spectra
SMILES:C(CC(=O)O)C(=O)C(=O)O
Studies:Available studies (via RefMet name)

Select appropriate tab below to view additional details:

External database links:

PubChem CID:51
CHEBI ID:30915
HMDB ID:HMDB0000208
KEGG ID:C00026
Chemspider ID:50
METLIN ID:5218
BMRB ID:bmse000937
MetaCyc ID:2-KETOGLUTARATE
NP-MRD ID(NMR):NP0000103
Plant Metabolite Hub(Pmhub):MS000000269

Calculated physicochemical properties (?):

Heavy Atoms: 10  
Rings: 0  
Aromatic Rings: 0  
Rotatable Bonds: 4  
van der Waals Molecular volume: 131.09 Å3 molecule-1  
Toplogical Polar Sufrace Area: 91.67 Å2 molecule-1  
Hydrogen Bond Donors: 2  
Hydrogen Bond Acceptors: 5  
logP: -0.50  
Molar Refractivity: 29.51  
Fraction sp3 Carbons: 0.40  
sp3 Carbons: 2  

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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