Metabolomics Structure Database

 
MW REGNO: 39106
Common Name:2-Methyl-3-hydroxy-5-formylpyridine-4-carboxylate
Systematic Name:5-formyl-3-hydroxy-2-methylpyridine-4-carboxylic acid
RefMet Name:2-Methyl-3-hydroxy-5-formylpyridine-4-carboxylate
Synonyms: [PubChem Synonyms]
Exact Mass:
181.0375 (neutral)    Calculate m/z:
Formula:C8H7NO4
InChIKey:JTWNWNJMNSJYDL-UHFFFAOYSA-N
ClassyFire superclass:Organoheterocyclic compounds [C0000002]
ClassyFire class:Pyridines and derivatives [C0000089]
ClassyFire subclass:Pyridinecarboxylic acids and derivatives [C0001322]
ClassyFire direct parent:Pyridinecarboxylic acids [C0002414]
SMILES:Cc1c(c(c(cn1)C=O)C(=O)O)O
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:440898
CHEBI ID:28038
HMDB ID:HMDB0006954
KEGG ID:C06050
Chemspider ID:389728
Plant Metabolite Hub(Pmhub):MS000018982

Calculated physicochemical properties (?):

Heavy Atoms: 13  
Rings: 1  
Aromatic Rings: 1  
Rotatable Bonds: 2  
van der Waals Molecular volume: 156.66 Å3 molecule-1  
Toplogical Polar Sufrace Area: 87.49 Å2 molecule-1  
Hydrogen Bond Donors: 2  
Hydrogen Bond Acceptors: 5  
logP: 0.61  
Molar Refractivity: 42.99  
Fraction sp3 Carbons: 0.12  
sp3 Carbons: 1  

Human Pathway links:

HMDB and KEGG 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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