| Weight | 290.447 g/mol |
|---|---|
| Formula | C19H30O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
EPIANDROSTERONE (481-29-8)
Androsterone · 5 alpha Androstan 3 alpha ol 17 one · 5 alpha-Androstan-3 alpha-ol-17-one
Score:
#1782 in Biochemistry
,
#3901 in Biology
,
#4913 in Chemistry
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- The conversion of testosterone to 5-alpha-androstan-17-beta-ol-3-one by rat prostate in vivo and in vitro. (Journal of Biological Chemistry, 1968)
- The intranuclear binding of testosterone and 5-alpha-androstan-17-beta-ol-3-one by rat prostate. (Journal of Biological Chemistry, 1968)
- DEHYDROEPIANDROSTERONE AND ANDROSTERONE LEVELS IN HUMAN PLASMA. EFFECT OF AGE AND SEX; DAY-TO-DAY AND DIURNAL VARIATIONS* (The Journal of Clinical Endocrinology and Metabolism, 1957)
- The conversion of testosterone to 5 alpha-androstan-17 beta-ol-3-one (dihydrotestosterone) by skin slices of man. (Journal of Clinical Investigation, 1969)
- EXPERIMENTAL EVALUATION OF AN ORALLY ACTIVE COMBINATION OF ANDROSTERONE WITH ETHYL CHLOROPHENOXYISOBUTYRATE (The Lancet, 1962)
- Selectivity of substrate (trifluoperazine) and inhibitor (amitriptyline, androsterone, canrenoic acid, hecogenin, phenylbutazone, quinidine, quinine, and sulfinpyrazone) "probes" for human udp-glucuronosyltransferases. (Drug Metabolism and Disposition, 2005)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Androsterone
- 5 alpha Androstan 3 alpha ol 17 one
- 5 alpha-Androstan-3 alpha-ol-17-one
- 3-alpha-Hydroxy-5-alpha-Androstan-17-One
- 3 alpha Hydroxy 5 alpha Androstan 17 One
-
SMILESCC12CCC(CC1CCC3C2CCC4(C3CCC4=O)C)O
-
InChIKeyQGXBDMJGAMFCBF-UHFFFAOYSA-N
- Pubchem - EPIANDROSTERONE
- Wikipedia - epiandrosterone
Epiandrosterone, or isoandrosterone, also known as 3-androsterone, 3-hydroxy-5-androstan-17-one, or 5-androstan-3-ol-17-one, is a steroid hormone with weak androgenic activity. It is a metabolite of testosterone and dihydrotestosterone (DHT). It was first isolated in 1931, by Adolf Friedrich Johann Butenandt and Kurt Tscherning.
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