CAS 10417-86-4
:5β-Pregnan-21-ol-3,11,20-trione
Description:
5β-Pregnan-21-ol-3,11,20-trione, also known as 5β-pregnane-3,11,20-trione, is a steroid compound characterized by its specific structural features, including a pregnane backbone with three ketone groups at positions 3, 11, and 20. This compound is a derivative of progesterone and is part of the larger class of steroid hormones. It is typically found in various biological systems and can be involved in metabolic pathways related to steroidogenesis. The presence of multiple carbonyl groups contributes to its reactivity and potential biological activity, influencing processes such as hormone regulation and signaling. The compound is of interest in both pharmacological and biochemical research, particularly in studies related to reproductive health and endocrine function. Its CAS number, 10417-86-4, serves as a unique identifier for regulatory and research purposes, facilitating the tracking of its properties and applications in scientific literature.
Formula:C21H30O4
InChI:InChI=1S/C21H30O4/c1-20-8-7-13(23)9-12(20)3-4-14-15-5-6-16(18(25)11-22)21(15,2)10-17(24)19(14)20/h12,14-16,19,22H,3-11H2,1-2H3/t12-,14+,15+,16-,19-,20+,21+/m1/s1
InChI key:InChIKey=ZDUVZJUTJOBJHS-XYEQKYNMSA-N
SMILES:C[C@@]12[C@@]3([C@]([C@]4([C@](C)(CC3=O)[C@@H](C(CO)=O)CC4)[H])(CC[C@@]1(CC(=O)CC2)[H])[H])[H]
Synonyms:- (5Beta)-21-Hydroxypregnane-3,11,20-Trione
- (5β)-21-Hydroxypregnane-3,11,20-trione
- 21-Hydroxy-5beta-pregnane-3,11,20-trione
- 5β-Pregnan-21-ol-3,11,20-trione
- 5β-Pregnane-3,11,20-trione, 21-hydroxy-
- NSC 79098
- Pregnane-3,11,20-trione, 21-hydroxy-, (5β)-
- DHA
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Found 2 products.
5β-Pregnan-21-ol-3,11,20-trione
CAS:Controlled Product<p>Applications 5β-Pregnan-21-ol-3,11,20-trione is a metabolite of corticosterone.<br>References Jellinck, P.H., et. al.: J. Steroid Biochem., 71, 139 (1999)<br></p>Formula:C21H30O4Color and Shape:NeatMolecular weight:346.4615β-Pregnan-21-ol-3,11,20-trione
CAS:Controlled Product<p>5Beta-Pregnan-21-ol-3,11,20-trione is a steroid derivative, which is commonly sourced from the metabolic pathways of corticosteroids. Its mode of action involves interaction with steroid receptors, functioning primarily in the modulation of biological processes that are sensitive to glucocorticoids. This compound is particularly valuable in the study of steroid metabolism and in exploring the structural-activity relationship inherent in steroid hormones.</p>Formula:C21H30O4Purity:Min. 95%Molecular weight:346.50 g/mol

