Substance

ID:312312

trans-Dehydroandrosterone

Names and Identifiers
Synonyms
反式-脱氢雄甾酮普拉睾酮去氢表雄酮脱氢异雄酮雄素-5-烯-3β-醇-17-酮DHEA3β-羟基-5-雄烯-17-酮trans-Dehydroandrosterone5-Androsten-3β-ol-17-onePrasteroneDehydroepiandrosteroneDehydroisoandrosterone3β-Hydroxy-5-androsten-17-one
IUPAC Traditional name
dehydroepiandrosterone
IUPAC name
(1S,2R,5S,10R,11S,15S)-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.02,7.011,15]heptadec-7-en-14-one
Registration numbers
Beilstein Number
CAS Number
MDL Number
EC Number
Properties
Product Information
Purity
97%
Empirical Formula (Hill Notation)
C19H28O2
Safety Information
GHS Hazard statements
H315-H319-H335
Drug Control
regulated under CDSA - not available from Sigma-Aldrich Canada
GHS Signal Word
Warning
Safety Statements
26-36
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
RTECS
BV8396000
MSDS Link
Risk Statements
36/37/38
GHS Pictograms
GHS07
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
German water hazard class
2
European Hazard Symbols
Irritant Irritant (Xi)
GHS Precautionary statements
P261-P305+P351+P338
Physical Property
Melting Point
149-151 °C(lit.)
Optical Rotation
[α]25/D +13.0°, c = 1 in ethanol
Molecule Details
Biochem/physiol Actions
Negative modulator of GABAA receptors. Steroid secreted by the adrenal gland with both estrogenic and androgenic properties. Its conversion to 5-androstenediol, a potent estrogen, enhances the growth and survival of estrogen-sensitive breast tumors. At high but physiologically valid concentrations, DHEA inhibits proliferation of chromaffin progenitor cells and induces dopaminergic differentiation.1
Molecular Spectra
No Data Available
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References
No Data Available
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