Metabolomics Structure Database

 
MW REGNO: 70443
Common Name:Verbascoside
Systematic Name:[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxy-tetrahydropyran-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate
RefMet Name:Verbascoside
Synonyms:Acteoside; Kusaginin; TJC 160; NSC 603831 [PubChem Synonyms]
Exact Mass:
624.2054 (neutral)    Calculate m/z:
Formula:C29H36O15
InChIKey:FBSKJMQYURKNSU-ZLSOWSIRSA-N
ClassyFire superclass:Phenylpropanoids and polyketides
ClassyFire class:Cinnamic acids and derivatives
ClassyFire subclass:Hydroxycinnamic acids and derivatives
ClassyFire direct parent:Coumaric acids and derivatives
NP-MRD NMR spectra:View NMR spectra
SMILES:C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@@H]1[C@H]([C@H](OCCc2ccc(c(c2)O)O)O[C@H](CO)[C@H]1OC(=O)/C=C/c1ccc(c(c1)O)O)O)O)O)O
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:5281800
KEGG ID:C10501
NP-MRD ID(NMR):NP0030572
Plant Metabolite Hub(Pmhub):MS000011021

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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