Metabolomics Structure Database

 
MW REGNO: 41989
Common Name:Vanillin
Systematic Name:4-hydroxy-3-methoxybenzaldehyde
RefMet Name:Vanillin
Synonyms: [PubChem Synonyms]
Exact Mass:
152.0473 (neutral)    Calculate m/z:
Formula:C8H8O3
InChIKey:MWOOGOJBHIARFG-UHFFFAOYSA-N
LIPID MAPS Category:Polyketides
LIPID MAPS mainclass:Phenolic acids
LIPID MAPS subclass:Phenolic acids
Massbank MS spectra:View MS spectra
SMILES:COc1cc(ccc1O)C=O
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:1183
CHEBI ID:18346
HMDB ID:HMDB0012308
KEGG ID:C00755
Chemspider ID:13860434
BMRB ID:bmse010006
MetaCyc ID:VANILLIN
EPA CompTox DB:DTXCID301969
Plant Metabolite Hub(Pmhub):MS000001893
PhytoHub ID:PHUB000645

Calculated physicochemical properties (?):

Heavy Atoms: 11  
Rings: 1  
Aromatic Rings: 1  
Rotatable Bonds: 2  
van der Waals Molecular volume: 139.51 Å3 molecule-1  
Toplogical Polar Sufrace Area: 46.53 Å2 molecule-1  
Hydrogen Bond Donors: 1  
Hydrogen Bond Acceptors: 3  
logP: 1.21  
Molar Refractivity: 40.05  
Fraction sp3 Carbons: 0.12  
sp3 Carbons: 1  

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
NPClassifier classification: "NPClassifier: A Deep Neural Network-Based Structural Classification Tool for Natural Products", Kim HW, Wang M, Leber CA, Nothias LF, Reher R, Kang KB, van der Hooft JJJ, Dorrestein PC, Gerwick WH and Cottrell GW. J Nat Prod. 2021 Nov 26;84(11):2795-2807.DOI: 10.1021/acs.jnatprod.1c00399.

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