CAS 739-26-4
:11β-Hydroxyetiocholanolone
Description:
11β-Hydroxyetiocholanolone, also known as 11β-hydroxyandrostenedione, is a steroid hormone that is a metabolite of testosterone and plays a role in the biosynthesis of other steroid hormones. It is characterized by its hydroxyl group at the 11β position, which distinguishes it from other androgens. This compound is typically found in the adrenal glands and is involved in various physiological processes, including the regulation of metabolism and immune response. Its chemical structure includes a steroid backbone, which is common to all steroid hormones, and it exhibits both anabolic and androgenic properties. The substance is of interest in both clinical and research settings, particularly in studies related to hormonal balance, athletic performance, and endocrine disorders. Due to its potential effects on muscle growth and recovery, it has also been scrutinized in the context of sports and anti-doping regulations. As with many steroids, its use and distribution are regulated in many countries due to potential side effects and health risks associated with misuse.
Formula:C19H30O3
InChI:InChI=1S/C19H30O3/c1-18-8-7-12(20)9-11(18)3-4-13-14-5-6-16(22)19(14,2)10-15(21)17(13)18/h11-15,17,20-21H,3-10H2,1-2H3/t11-,12-,13+,14+,15+,17-,18+,19+/m1/s1
InChI key:InChIKey=PIXFHVWJOVNKQK-DLAZEALESA-N
SMILES:C[C@@]12[C@@]3([C@]([C@]4([C@](C)(C[C@@H]3O)C(=O)CC4)[H])(CC[C@@]1(C[C@H](O)CC2)[H])[H])[H]
Synonyms:- (3α,5β,11β)-3,11-Dihydroxyandrostan-17-one
- 11β-Hydroxyaetiocholanolone
- 3-Alpha,11-Beta-Dihydroxy-5-Beta-Androstan-17-One
- 3α,11β-Dihydroxy-5β-androstan-17-one
- 3α,11β-Dihydroxy-5β-androstane-17-one
- 3α,11β-Dihydroxyetiocholan-17-one
- 5β-Androstan-17-one, 3α,11β-dihydroxy-
- 5β-Androstan-3α,11β-diol-17-one
- 5β-Androstane-3α,11β-diol-17-one
- Androstan-17-one, 3,11-dihydroxy-, (3α,5β,11β)-
- Ba 2686
- NSC 53897
- See more synonyms
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Found 7 products.
11b-Hydroxy etiocholanolone
CAS:Controlled Product<p>11b-Hydroxy etiocholanolone is a major metabolite of 11-ketotestosterone. It is formed from the reaction of 11-ketotestosterone with either carbon disulphide or plasma cortisol. The physiological levels of 11b-hydroxy etiocholanolone are not well known, but it has been observed that there are higher levels in women than in men. This metabolite is an active form of testosterone and can be detected in urine samples. 11b-hydroxy etiocholanolone has been shown to have a biphasic response to testosterone treatment, where it increases at low concentrations and decreases at high concentrations. This metabolite is also involved in the synthesis of estradiol through the side chain cleavage, which leads to a chromatographic peak during gas chromatography analysis.</p>Formula:C19H30O3Purity:Min. 95%Color and Shape:White PowderMolecular weight:306.44 g/mol11b-Hydroxy Etiocholanolone
CAS:Controlled Product<p>Applications A metabolite of Etiocholanolone.<br>References Eriksson, H., et al.: Eur. J. Biochem., 15, 132 (1970), Cook, D., et al.: Endocrinology, 93, 1019 (1973),<br></p>Formula:C19H30O3Color and Shape:White To Off-WhiteMolecular weight:306.4411β-Hydroxy Etiocholanolone-d4
CAS:Controlled ProductFormula:C19D4H26O3Color and Shape:NeatMolecular weight:310.46411β-hydroxy Etiocholanolone
CAS:<p>11β-Hydroxyetiocholanolone, a hydrocortisone metabolite, exhibits elevated fecal levels in giraffes (G. camelopardalis) and plains zebras (E. quagga) in response to environmental stress.</p>Formula:C19H30O3Color and Shape:SolidMolecular weight:306.44



