Record Information
Version1.0
Creation Date2016-09-30 23:01:48 UTC
Update Date2020-05-11 20:56:00 UTC
BMDB IDBMDB0002833
Secondary Accession Numbers
  • BMDB02833
Metabolite Identification
Common NameTestosterone sulfate
DescriptionTestosterone sulfate, also known as 17-O-sulfotestosterone or androgel, belongs to the class of organic compounds known as sulfated steroids. These are sterol lipids containing a sulfate group attached to the steroid skeleton. Testosterone sulfate is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.
Structure
Thumb
Synonyms
ValueSource
Testosterone-17beta-sulfateChEBI
Testosterone-17b-sulfateGenerator
Testosterone-17b-sulfuric acidGenerator
Testosterone-17b-sulphateGenerator
Testosterone-17b-sulphuric acidGenerator
Testosterone-17beta-sulfuric acidGenerator
Testosterone-17beta-sulphateGenerator
Testosterone-17beta-sulphuric acidGenerator
Testosterone-17β-sulfateGenerator
Testosterone-17β-sulfuric acidGenerator
Testosterone-17β-sulphateGenerator
Testosterone-17β-sulphuric acidGenerator
Testosterone sulfuric acidGenerator
Testosterone sulphateGenerator
Testosterone sulphuric acidGenerator
17-O-SulfotestosteroneHMDB
17beta-(Sulfooxy)androst-4-en-3-oneHMDB
Testosterone 17-sulfateHMDB
Testosterone 17-sulphateHMDB
Testosterone 17b-sulfateHMDB
Testosterone 17b-sulphateHMDB
Testosterone hydrogen sulfateHMDB
Testosterone hydrogen sulphateHMDB
Testosterone monosulfateHMDB
Testosterone monosulphateHMDB
Testosterone-17-sulfateHMDB
Testosterone-17-sulphateHMDB
AndroGelHMDB
AstraZeneca brand OF testosteroneHMDB
GlaxoSmithKline brand OF testosteroneHMDB
Hauck brand OF testosteroneHMDB
Schering brand OF testosteroneHMDB
TestolinHMDB
Testosterone-17-sulfate, (17alpha)-isomerHMDB
Testosterone-17-sulfate, ammonium saltHMDB
Testosterone-17-sulfate, sodium saltHMDB
17 beta Hydroxy 4 androsten 3 oneHMDB
17 beta Hydroxy 8 alpha 4 androsten 3 oneHMDB
HisteroneHMDB
SustanonHMDB
17-beta-Hydroxy-4-androsten-3-oneHMDB
Faulding brand OF testosteroneHMDB
Ferring brand OF testosteroneHMDB
8 IsotestosteroneHMDB
8-IsotestosteroneHMDB
Paladin brand OF testosteroneHMDB
Pasadena brand OF testosteroneHMDB
Solvay brand OF testosteroneHMDB
SterotateHMDB
TestosteroneHMDB
Unimed brand OF testosteroneHMDB
Dr. kade brand OF testosteroneHMDB
TestimHMDB
TestopelHMDB
AndropatchHMDB
CEPA brand OF testosteroneHMDB
Ortho brand OF testosteroneHMDB
17-beta-Hydroxy-8 alpha-4-androsten-3-oneHMDB
Auxilium pharmaceuticals inc. brand OF testosteroneHMDB
Bartor brand OF testosteroneHMDB
Ulmer brand OF testosteroneHMDB
Watson brand OF testosteroneHMDB
AndrodermHMDB
AndrotopHMDB
SmithKline beecham brand OF testosteroneHMDB
TestodermHMDB
Chemical FormulaC19H28O5S
Average Molecular Weight368.488
Monoisotopic Molecular Weight368.165744696
IUPAC Name[(1S,2R,10R,11S,14S,15S)-2,15-dimethyl-5-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-6-en-14-yl]oxidanesulfonic acid
Traditional Nametestosterone sulfate
CAS Registry Number651-45-6
SMILES
[H][C@@]12CC[C@H](OS(O)(=O)=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CCC2=CC(=O)CC[C@]12C
InChI Identifier
InChI=1S/C19H28O5S/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(24-25(21,22)23)19(15,2)10-8-16(14)18/h11,14-17H,3-10H2,1-2H3,(H,21,22,23)/t14-,15-,16-,17-,18-,19-/m0/s1
InChI KeyWAQBISPOEAOCOG-DYKIIFRCSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as sulfated steroids. These are sterol lipids containing a sulfate group attached to the steroid skeleton.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassSteroids and steroid derivatives
Sub ClassSulfated steroids
Direct ParentSulfated steroids
Alternative Parents
Substituents
  • Sulfated steroid skeleton
  • Androgen-skeleton
  • Androstane-skeleton
  • 3-oxo-delta-4-steroid
  • 3-oxosteroid
  • Oxosteroid
  • Delta-4-steroid
  • Cyclohexenone
  • Sulfuric acid ester
  • Alkyl sulfate
  • Sulfate-ester
  • Sulfuric acid monoester
  • Organic sulfuric acid or derivatives
  • Ketone
  • Cyclic ketone
  • Organic oxygen compound
  • Carbonyl group
  • Organooxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Aliphatic homopolycyclic compound
Molecular FrameworkAliphatic homopolycyclic compounds
External Descriptors
Ontology
StatusDetected but not Quantified
Origin
  • Endogenous
  • Exogenous
BiofunctionNot Available
ApplicationNot Available
Cellular locations
  • Cell membrane
  • Cytoplasm
  • Membrane
Physical Properties
StateSolid
Experimental Properties
PropertyValueReference
Melting Point155 - 156 °CNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP0.13ALOGPS
logP3.42ChemAxon
logS-4.7ALOGPS
pKa (Strongest Acidic)-1.3ChemAxon
pKa (Strongest Basic)-4.8ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area80.67 ŲChemAxon
Rotatable Bond Count2ChemAxon
Refractivity94.42 m³·mol⁻¹ChemAxon
Polarizability39.59 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash Key
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positivesplash10-0f76-0479000000-bdb3d4908eb17de0bf8eView in MoNA
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, PositiveNot AvailableView in JSpectraViewer
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-014i-0039000000-3c70201ac318944d2318View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-00di-0291000000-40eaf6c5a80279466483View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0udl-4973000000-432f25c70a6a5a3f7b22View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-014i-0029000000-c0079f3c134f1d99c4edView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-00kr-1092000000-705a336c46754ed24422View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-008i-4090000000-c74eaf7f9b7239e6720bView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-014i-0009000000-c58c9c29bacda1fca240View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-014j-7009000000-fd0f50e05b7ebfdcc66aView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0002-9003000000-58fd5118dcd0e2d4f5c4View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-014i-0019000000-810038c8bedbbf20ea25View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0300-0891000000-45adc8bb06a4d3a47728View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0a4i-0910000000-abcfbb505d2cd01adbeaView in MoNA
Biological Properties
Cellular Locations
  • Cell membrane
  • Cytoplasm
  • Membrane
Biospecimen Locations
  • Brain
  • Kidney
  • Liver
  • Placenta
  • Skeletal Muscle
  • Testis
  • Urine
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BrainExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
details
KidneyExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
details
LiverExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
details
PlacentaExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
details
Skeletal MuscleExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
details
TestisExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
details
Abnormal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
UrineDetected but not QuantifiedNot QuantifiedNot SpecifiedNot Specified
Treated with steroids
details
UrineDetected but not QuantifiedNot QuantifiedNot SpecifiedNot Specified
Treated with steroids
details
HMDB IDHMDB0002833
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB023072
KNApSAcK IDNot Available
Chemspider ID106493
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG ID2794968
Wikipedia LinkTestosterone sulfate
METLIN ID3558
PubChem Compound119207
PDB IDNot Available
ChEBI ID84094
References
Synthesis ReferenceHolden, G. W.; Levi, I.; Bromley, R. Sodium testosterone sulfate. Journal of the American Chemical Society (1949), 71 3844.
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available