Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	37557
Common Name:	Phosphohydroxypyruvic acid
Systematic Name:	2-oxo-3-(phosphonooxy)propanoic acid
RefMet Name:	Phosphohydroxypyruvic acid
Synonyms:	[PubChem Synonyms]
Exact Mass:	183.9773 (neutral)    Calculate m/z: (Choose adduct) [M+H]+ [M+H-H2O]+ [M.]+ [M+2H]2+ [M+3H]3+ [M+4H]4+ [M+K]+ [M+2K]2+ [M-H+2K]+ [M+Na]+ [M+2Na]2+ [M-H+2Na]+ [M+Li]+ [M+2Li]2+ [M+NH4]+ [M-H]- [M-2H]2- [M-3H]3- [M-4H]4- [M+Cl]- [M+OAc]- [M+HCOO]- M(neutral)
Formula:	C3H5O7P
InChIKey:	LFLUCDOSQPJJBE-UHFFFAOYSA-N
ClassyFire superclass:	Organic oxygen compounds [C0004603]
ClassyFire class:	Organooxygen compounds [C0000323]
ClassyFire subclass:	Carbonyl compounds [C0001831]
ClassyFire direct parent:	Glycerone phosphates [C0003446]
SMILES:	C(C(=O)C(=O)O)OP(=O)(O)O
Studies:	Available studies (via RefMet name)

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All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	105
CHEBI ID:	30933
HMDB ID:	HMDB0001024
KEGG ID:	C03232
Chemspider ID:	103
METLIN ID:	484
MetaCyc ID:	3-P-HYDROXYPYRUVATE
Plant Metabolite Hub(Pmhub):	MS000017859

Calculated physicochemical properties (?):

Heavy Atoms:	11
Rings:	0
Aromatic Rings:	0
Rotatable Bonds:	4
van der Waals Molecular volume:	136.54 Å3 molecule-1
Toplogical Polar Sufrace Area:	121.13 Å2 molecule-1
Hydrogen Bond Donors:	3
Hydrogen Bond Acceptors:	7
logP:	-0.62
Molar Refractivity:	30.85
Fraction sp3 Carbons:	0.33
sp3 Carbons:	1

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