Metabolomics Structure Database

 
MW REGNO: 48490
Common Name:6''-O-Malonylglycitin
Systematic Name:3-oxo-3-{[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-{[3-(4-hydroxyphenyl)-6-methoxy-4-oxo-4H-chromen-7-yl]oxy}oxan-2-yl]methoxy}propanoic acid
RefMet Name:Glycitein 6''-O-malonylglucoside
Synonyms: [PubChem Synonyms]
Exact Mass:
532.1217 (neutral)    Calculate m/z:
Formula:C25H24O13
InChIKey:OWMHCYFEIJPHFB-GOZZSVHWSA-N
ClassyFire superclass:Phenylpropanoids and polyketides
ClassyFire class:Isoflavonoids
ClassyFire subclass:Isoflavonoid O-glycosides
ClassyFire direct parent:Isoflavonoid O-glycosides
Massbank MS spectra:View MS spectra
SMILES:COc1cc2c(cc1O[C@H]1[C@@H]([C@H]([C@@H]([C@@H](COC(=O)CC(=O)O)O1)O)O)O)occ(c1ccc(cc1)O)c2=O
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:23724657
HMDB ID:HMDB0039323
KEGG ID:C16197
Plant Metabolite Hub(Pmhub):MS000108165

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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