Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	36956
Common Name:	Pregnenolone sulfate
Systematic Name:	20-oxopregn-5-en-3beta-yl sulfate
RefMet Name:	Pregnenolone sulfate
Synonyms:	(3beta)-3-(sulfooxy)pregn-5-en-20-one; 5-pregnen-3beta-ol-20-one sulfate; pregnenolone sulfate [PubChem Synonyms]
Exact Mass:	396.1970 (neutral)    Calculate m/z: (Choose adduct) [M+H]+ [M+H-H2O]+ [M.]+ [M+2H]2+ [M+3H]3+ [M+4H]4+ [M+K]+ [M+2K]2+ [M-H+2K]+ [M+Na]+ [M+2Na]2+ [M-H+2Na]+ [M+Li]+ [M+2Li]2+ [M+NH4]+ [M-H]- [M-2H]2- [M-3H]3- [M-4H]4- [M+Cl]- [M+OAc]- [M+HCOO]- M(neutral)
Formula:	C21H32O5S
InChIKey:	DIJBBUIOWGGQOP-QGVNFLHTSA-N
LIPID MAPS Category:	Sterol Lipids [ST]
LIPID MAPS mainclass:	Steroid conjugates [ST05]
LIPID MAPS subclass:	Sulfates [ST0502]
NP-MRD NMR spectra:	View NMR spectra
SMILES:	CC(=O)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@H](CC[C@]4(C)[C@H]3CC[C@]12C)OS(=O)(=O)O
Studies:	Available studies (via RefMet name)

Select appropriate tab below to view additional details:

All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	105074
LIPID MAPS ID:	LMST05020014
CHEBI ID:	35420
HMDB ID:	HMDB0060382
KEGG ID:	C18044
NP-MRD ID(NMR):	NP0000939
Plant Metabolite Hub(Pmhub):	MS000026316

Calculated physicochemical properties (?):

Heavy Atoms:	27
Rings:	4
Aromatic Rings:	0
Rotatable Bonds:	3
van der Waals Molecular volume:	379.60 Å3 molecule-1
Toplogical Polar Sufrace Area:	80.67 Å2 molecule-1
Hydrogen Bond Donors:	1
Hydrogen Bond Acceptors:	5
logP:	5.88
Molar Refractivity:	102.71
Fraction sp3 Carbons:	0.86
sp3 Carbons:	18

Human Pathway links:

REACTOME 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