Metabolomics Structure Database

 
MW REGNO: 69316
Common Name:Pinocembrin 7-rhamnosylglucoside
Systematic Name:(2S)-7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxy-tetrahydropyran-2-yl]oxy-5-hydroxy-2-phenyl-chroman-4-one
Synonyms:AC1L9CUZ; C09828 [PubChem Synonyms]
Exact Mass:
564.1843 (neutral)    Calculate m/z:
Formula:C27H32O13
InChIKey:UVPBNPUZWAOBQX-AFUJZTQMSA-N
ClassyFire superclass:Phenylpropanoids and polyketides
ClassyFire class:Flavonoids
ClassyFire subclass:Flavonoid glycosides
ClassyFire direct parent:Flavonoid-7-O-glycosides
SMILES:C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@@H]1[C@H]([C@@H]([C@@H](CO)O[C@H]1Oc1cc(c2C(=O)C[C@@H](c3ccccc3)Oc2c1)O)O)O)O)O)O
Studies:Available studies(via PubChem CID)

Select appropriate tab below to view additional details:

External database links:

PubChem CID:442454
LIPID MAPS ID:LMPK12140136
KEGG ID:C09828
EPA CompTox DB:DTXCID60964316
Plant Metabolite Hub(Pmhub):MS000021057

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.

  logo