Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	68719
Common Name:	6-Hydroxykynurenic acid
Systematic Name:	6-hydroxy-4-oxo-1H-quinoline-2-carboxylic acid
RefMet Name:	6-Hydroxykynurenic acid
Synonyms:	6-hydroxy-4-oxo-1H-quinoline-2-carboxylic acid; 6-Hydroxykynurenate; SureCN975885; SureCN4516264 [PubChem Synonyms]
Exact Mass:	205.0375 (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:	C10H7NO4
InChIKey:	CQUUHDQRJWXDPY-UHFFFAOYSA-N
ClassyFire superclass:	Organoheterocyclic compounds [C0000002]
ClassyFire class:	Quinolines and derivatives [C0001253]
ClassyFire subclass:	Quinoline carboxylic acids [C0002552]
ClassyFire direct parent:	Quinoline carboxylic acids [C0002552]
SMILES:	c1cc2c(cc1O)c(=O)cc(C(=O)O)[nH]2
Studies:	Available studies (via RefMet name)

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All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	440752
CHEBI ID:	2195
HMDB ID:	HMDB0033528
KEGG ID:	C05663
EPA CompTox DB:	DTXCID801194244
Plant Metabolite Hub(Pmhub):	MS000016174

Calculated physicochemical properties (?):

Heavy Atoms:	15
Rings:	2
Aromatic Rings:	2
Rotatable Bonds:	1
van der Waals Molecular volume:	165.36 Å3 molecule-1
Toplogical Polar Sufrace Area:	90.39 Å2 molecule-1
Hydrogen Bond Donors:	3
Hydrogen Bond Acceptors:	4
logP:	1.68
Molar Refractivity:	53.23
Fraction sp3 Carbons:	0.00
sp3 Carbons:	0

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