Metabolomics Structure Database

 
MW REGNO: 206760
Common Name:4-Hydroxy-duloxetine glucuronide
Systematic Name:(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[[4-[(1S)-3-(methylamino)-1-(2-thienyl)propoxy]-1-naphthyl]oxy]tetrahydropyran-2-carboxylic acid
RefMet Name:4-Hydroxy-duloxetine glucuronide
Synonyms:Duloxetine 4-hydroxyglucuronide; 4-Hydroxy Duloxetine b-D-Glucuronide [PubChem Synonyms]
Exact Mass:
489.1457 (neutral)    Calculate m/z:
Formula:C24H27NO8S
InChIKey:OBIZFSZXDHWUJZ-ANUWOGMRSA-N
ClassyFire superclass:Organic oxygen compounds
ClassyFire class:Organooxygen compounds
ClassyFire subclass:Carbohydrates and carbohydrate conjugates
ClassyFire direct parent:Phenolic glycosides
SMILES:CNCC[C@@H](c1cccs1)Oc1ccc(c2ccccc12)O[C@H]1[C@@H]([C@H]([C@@H]([C@@H](C(=O)O)O1)O)O)O
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:29981513
CHEBI ID:169567
HMDB ID:HMDB0060763

Calculated physicochemical properties:

No data available

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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