| Names | |
|---|---|
| IUPAC name 5β-Androstane-3β,17β-diol | |
| Systematic IUPAC name (1S,3aS,3bR,5aR,7S,9aS,9bS,11aS)-9a,11a-Dimethylhexadecahydro-1H-cyclopenta[a]phenanthrene-1,7-diol | |
| Other names Epietiocholanediol; Etiocholane-3β,17β-diol | |
| Identifiers | |
3D model (JSmol) | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| UNII | |
| |
| |
| Properties | |
| C19H32O2 | |
| Molar mass | 292.463 g·mol−1 |
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa). | |
3β-Etiocholanediol, orepietiocholanediol, also known as3β,5β-androstanediol or asetiocholane-3β,17β-diol, is anaturally occurringetiocholane (5β-androstane)steroid and anendogenousmetabolite oftestosterone. It is formed from5β-dihydrotestosterone (after5β-reduction of testosterone) and is transformed intoepietiocholanolone.[1]
Thisbiochemistry article is astub. You can help Wikipedia byadding missing information. |