| Weight | 368.495 g/mol |
|---|---|
| Formula | C19H28O5S |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
Prasterone sulfate (651-48-9)
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- The Effects of Grinding and Drying on the Solid State Stability of Sodium Prasterone Sulfate (Chemical & Pharmaceutical Bulletin, 1982)
- Stability of lyophilized sodium prasterone sulfate. (Journal of parenteral science and technology : a publication of the Parenteral Drug Association, 1981)
- The Properties of Water of Crystallization of Sodium Prasterone Sulfate (Chemical & Pharmaceutical Bulletin, 1981)
- The Biological Fate of Sodium Prasterone Sulfate after Vaginal Administration. I. Absorption and Excretion in Rats (Journal of pharmacobio-dynamics, 1992)
- Contributions of Various Serum Proteins to the Binding of Prasterone Sulfate in Humans (Chemical & Pharmaceutical Bulletin, 1992)
- The Biological Fate of Sodium Prasterone Sulfate after Vaginal Administration II: Distribution after Single and Multiple Administration to Pregnant Rats. (Drug Metabolism and Pharmacokinetics, 1992)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESCC12CCC3C(C1CCC2=O)CC=C4C3(CCC(C4)OS(=O)(=O)O)C
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InChIKeyCZWCKYRVOZZJNM-UHFFFAOYSA-N
- Pubchem - Prasterone sulfate
- Wikipedia - prasterone sulfate
Prasterone sulfate (brand names Astenile, Levospa, Mylis, Teloin), also known as dehydroepiandrosterone sulfate (DHEA-S), is a naturally occurring androstane steroid which is marketed and used in Japan as a labor inducer in the treatment of insufficient cervical ripening and dilation during childbirth. It is the C3 sulfate ester of prasterone (dehydroepiandrosterone; DHEA), and is known to act as a prohormone of DHEA and by extension of androgens and estrogens, although it also has its own activity as a neurosteroid. Prasterone sulfate is used medically as the sodium salt via injection and is referred to by the name sodium prasterone sulfate (JAN).
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