Metabolomics Structure Database

 
MW REGNO: 52332
Common Name:(S)-3-phenyllactic acid
Systematic Name:(2S)-2-hydroxy-3-phenylpropanoic acid
RefMet Name:Phenyllactic acid
Synonyms: [PubChem Synonyms]
Exact Mass:
166.0630 (neutral)    Calculate m/z:
Formula:C9H10O3
InChIKey:VOXXWSYKYCBWHO-QMMMGPOBSA-N
ClassyFire superclass:Phenylpropanoids and polyketides [C0000261]
ClassyFire class:Phenylpropanoic acids [C0002551]
ClassyFire subclass:Phenylpropanoic acids [C0002551]
ClassyFire direct parent:Aromatic homomonocyclic compounds
Massbank MS spectra:View MS spectra
SMILES:c1ccc(cc1)C[C@@H](C(=O)O)O
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:444718
CHEBI ID:43065
HMDB ID:HMDB0000563
Plant Metabolite Hub(Pmhub):MS000000274

Calculated physicochemical properties (?):

Heavy Atoms: 12  
Rings: 1  
Aromatic Rings: 1  
Rotatable Bonds: 3  
van der Waals Molecular volume: 156.81 Å3 molecule-1  
Toplogical Polar Sufrace Area: 57.53 Å2 molecule-1  
Hydrogen Bond Donors: 2  
Hydrogen Bond Acceptors: 3  
logP: 0.96  
Molar Refractivity: 44.30  
Fraction sp3 Carbons: 0.22  
sp3 Carbons: 2  

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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