Metabolomics Structure Database

 
MW REGNO: 42476
Common Name:Coniferin
Systematic Name:(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-{4-[(1E)-3-hydroxyprop-1-en-1-yl]-2-methoxyphenoxy}oxane-3,4,5-triol
RefMet Name:Coniferin
Synonyms: [PubChem Synonyms]
Exact Mass:
342.1315 (neutral)    Calculate m/z:
Formula:C16H22O8
InChIKey:SFLMUHDGSQZDOW-FAOXUISGSA-N
ClassyFire superclass:Organic oxygen compounds
ClassyFire class:Organooxygen compounds
ClassyFire subclass:Carbohydrates and carbohydrate conjugates
ClassyFire direct parent:Phenolic glycosides
NP-MRD NMR spectra:View NMR spectra
SMILES:COc1cc(/C=C/CO)ccc1O[C@H]1[C@@H]([C@H]([C@@H]([C@@H](CO)O1)O)O)O
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:5280372
CHEBI ID:16220
HMDB ID:HMDB0013682
KEGG ID:C00761
Chemspider ID:4444067
BMRB ID:bmse000608
MetaCyc ID:CPD-1777
NP-MRD ID(NMR):NP0002813
Plant Metabolite Hub(Pmhub):MS000011532

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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