Metabolomics Structure Database

 
MW REGNO: 36910
Common Name:Testosterone glucuronide
Systematic Name:17beta-hydroxyandrost-4-en-3-one 3-D-glucuronide
RefMet Name:Testosterone glucuronide
Synonyms: [PubChem Synonyms]
Exact Mass:
464.2410 (neutral)    Calculate m/z:
Formula:C25H36O8
InChIKey:NIKZPECGCSUSBV-HMAFJQTKSA-N
LIPID MAPS Category:Sterol Lipids [ST]
LIPID MAPS mainclass:Steroid conjugates [ST05]
LIPID MAPS subclass:Glucuronides [ST0501]
MoNA MS spectra:View MS spectra
SMILES:C[C@]12CCC(=O)C=C1CC[C@H]1[C@@H]3CC[C@@H]([C@@]3(C)CC[C@H]21)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:108192
LIPID MAPS ID:LMST05010012
CHEBI ID:28835
HMDB ID:HMDB0003193
KEGG ID:C11134
Chemspider ID:97270
METLIN ID:2794
Plant Metabolite Hub(Pmhub):MS000004553

Calculated physicochemical properties (?):

Heavy Atoms: 33  
Rings: 5  
Aromatic Rings: 0  
Rotatable Bonds: 3  
van der Waals Molecular volume: 441.66 Å3 molecule-1  
Toplogical Polar Sufrace Area: 135.59 Å2 molecule-1  
Hydrogen Bond Donors: 4  
Hydrogen Bond Acceptors: 8  
logP: 3.51  
Molar Refractivity: 118.97  
Fraction sp3 Carbons: 0.84  
sp3 Carbons: 21  

Human Pathway links:

HMDB and KEGG pathways containing this metabolite

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

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