Metabolomics Structure Database

 
MW REGNO: 35312
Common Name:Androsterone
Systematic Name:3alpha-hydroxy-5alpha-androstan-17-one
RefMet Name:Androsterone
Synonyms:Androsterone [PubChem Synonyms]
Exact Mass:
290.2246 (neutral)    Calculate m/z:
Formula:C19H30O2
InChIKey:QGXBDMJGAMFCBF-HLUDHZFRSA-N
LIPID MAPS Category:Sterol Lipids [ST]
LIPID MAPS mainclass:Steroids [ST02]
LIPID MAPS subclass:C19 steroids (androgens) and derivatives [ST0202]
Massbank MS spectra:View MS spectra
NP-MRD NMR spectra:View NMR spectra
SMILES:C[C@]12CC[C@H](C[C@@H]1CC[C@H]1[C@@H]3CCC(=O)[C@@]3(C)CC[C@H]21)O
Studies:Available studies (via RefMet name)

Select appropriate tab below to view additional details:

External database links:

PubChem CID:5879
LIPID MAPS ID:LMST02020001
CHEBI ID:16032
HMDB ID:HMDB0000031
KEGG ID:C00523
BMRB ID:bmse000543
MetaCyc ID:ANDROSTERONE
NP-MRD ID(NMR):NP0002785
EPA CompTox DB:DTXCID70209568
Plant Metabolite Hub(Pmhub):MS000004151

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

  logo