Names | |
---|---|
IUPAC name 5β-Androstane-3α,17β-diol | |
Systematic IUPAC name (1S,3aS,3bR,5aR,7R,9aS,9bS,11aS)-9a,11a-Dimethylhexadecahydro-1H-cyclopentaphenanthrene-1,7-diol | |
Other names Etiocholanediol; Etiocholane-3α,17β-diol | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ChEBI | |
ChEMBL | |
ChemSpider | |
PubChem CID | |
UNII | |
InChI
| |
SMILES
| |
Properties | |
Chemical formula | C19H32O2 |
Molar mass | 292.463 g·mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references |
3α-Etiocholanediol, or simply etiocholanediol, also known as 3α,5β-androstanediol or as etiocholane-3α,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 further transformed into etiocholanolone.
See also
References
- PEARLMAN WH; CERCEO E (1948). "The isolation of pregnanol-3(alpha)-one-20,pregnanediol-3(alpha), 20(beta), and etiocholanediol-3(alpha),17(beta) from the bile of pregnant cows". The Journal of Biological Chemistry. 176 (2): 847–856. doi:10.1016/S0021-9258(19)52700-4. PMID 18889940.
External links
This article about a steroid is a stub. You can help Misplaced Pages by expanding it. |
This biochemistry article is a stub. You can help Misplaced Pages by expanding it. |