Metabolomics Structure Database

 
MW REGNO: 35325
Common Name:Dehydroepiandrosterone
Systematic Name:3beta-hydroxyandrost-5-en-17-one
RefMet Name:Dehydroepiandrosterone
Synonyms: [PubChem Synonyms]
Exact Mass:
288.2089 (neutral)    Calculate m/z:
Formula:C19H28O2
InChIKey:FMGSKLZLMKYGDP-USOAJAOKSA-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](CC1=CC[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:5881
LIPID MAPS ID:LMST02020021
CHEBI ID:28689
HMDB ID:HMDB0000077
KEGG ID:C01227
BMRB ID:bmse000665
MetaCyc ID:3-BETA-HYDROXYANDROST-5-EN-17-ONE
NP-MRD ID(NMR):NP0000667
EPA CompTox DB:DTXCID00209036
Plant Metabolite Hub(Pmhub):MS000000172

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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