Chemistry:3β-Etiocholanediol
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| Names | |
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| IUPAC name
5β-Androstane-3β,17β-diol
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| 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
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| Identifiers | |
3D model (JSmol)
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PubChem CID
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| Properties | |
| C19H32O2 | |
| Molar mass | 292.463 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Tracking categories (test):
3β-Etiocholanediol, or epietiocholanediol, also known as 3β,5β-androstanediol or as etiocholane-3β,17β-diol, is a naturally occurring etiocholane (5β-androstane) steroid and an endogenous metabolite of testosterone. It is formed from 5β-dihydrotestosterone (after 5β-reduction of testosterone) and is transformed into epietiocholanolone.[1]
See also
References
- ↑ "Metabolism of the steroid hormones; the isolation of etiocholanediol-3(alpha), 17(alpha) from human urine". Endocrinology 42 (3): 174–175. March 1948. doi:10.1210/endo-42-3-174. PMID 18914211.
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