CAS 2089-06-7
:5A-pregnane-3,11,20-trione
Description:
5A-pregnane-3,11,20-trione, with the CAS number 2089-06-7, is a steroid compound characterized by its three ketone functional groups located at positions 3, 11, and 20 of the pregnane backbone. This compound is a derivative of progesterone and is part of the larger class of steroid hormones, which are known for their significant biological activities. It is typically a white to off-white crystalline solid and is soluble in organic solvents. The presence of multiple carbonyl groups contributes to its reactivity and potential interactions with biological systems, particularly in relation to steroid hormone activity. 5A-pregnane-3,11,20-trione may be utilized in research settings to study steroid metabolism and hormonal regulation. Its structural features allow it to interact with steroid receptors, influencing various physiological processes. As with many steroid compounds, handling and usage should be approached with caution due to potential biological effects and regulatory considerations.
Formula:C21H30O3
InChI:InChI=1/C21H30O3/c1-12(22)16-6-7-17-15-5-4-13-10-14(23)8-9-20(13,2)19(15)18(24)11-21(16,17)3/h13,15-17,19H,4-11H2,1-3H3/t13-,15-,16+,17-,19+,20-,21+/m0/s1
Synonyms:- (5S,8S,9S,10S,13S,14S,17S)-17-ACETYL-10,13-DIMETHYL-TETRADECAHYDRO-CYCLOPENTA[A]PHENANTHRENE-3,11-DIONE
- 5-ALPHA-DIHYDRO-11-KETOPROGESTERONE
- ALLOPREGNANETRIONE
- 5-ALPHA-PREGNAN-3,11,20-TRIONE
- 5ALPHA-PREGNANE-3,11,20-TRIONE
- ALLOPREGNANTRIONE
- 5A-pregnane-3,11,20-trione
- P3421_FLUKA
- 5α-pregnane-3,11,20-trione
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Found 2 products.
5α-Pregnane-3,11,20-trione
CAS:Controlled Product<p>Pregnenolone is a pregnane steroid that is synthesized from cholesterol. It can be converted to other hormones, such as progesterone, androgens, estrogens, and glucocorticoids. Pregnenolone has a strong affinity for the progesterone receptor and is used in the treatment of polycystic ovarian syndrome. It also has an anti-inflammatory effect and may be useful in the treatment of cancer. Hydrocortisone acetate (HC) inhibits protein synthesis by binding to the DNA-dependent RNA polymerase II at the transcriptional level. HC also binds to other proteins involved in transcription or translation such as histones, ribosomes, and transfer RNA synthetases. This results in decreased production of proteins necessary for cell division or growth.</p>Formula:C21H30O3Purity:Min. 95%Color and Shape:White PowderMolecular weight:330.46 g/mol

