Interesting facts
Interesting Facts about [(8R,9S,13S,14S,17R)-17-hydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl] benzoate
This compound represents a fascinating class of chemicals known as steroids, specifically a derivative of a steroid molecule. Steroids play a critical role in biological systems, often functioning as hormones that regulate a variety of physiological processes. Here are some engaging highlights:
- Structure and Function: The complex stereochemistry of this compound, indicated by its multiple chiral centers, suggests that its three-dimensional shape is essential for its biological activity. In many cases, the chirality of a molecule can significantly influence its interaction with biological receptors.
- Uses in Medicine: Compounds similar to this one are frequently explored for their medicinal properties. They can act as anti-inflammatory agents, potential treatments for various diseases, and even as anabolic agents in sports.
- Source of Inspiration: Such compounds are often derived from natural sources like plants and animals, inspiring scientists to synthesize derivatives that may enhance desired effects while minimizing side effects.
- Research Significance: As research on hormonal pathways and steroid functions continues, compounds of this nature are invaluable to chemists and biochemists seeking to unlock new therapeutic avenues.
- Analytical Techniques: Analyzing the properties of this compound can involve advanced techniques such as NMR spectroscopy and mass spectrometry, helping scientists thoroughly explore its structure and function.
In summary, [(8R,9S,13S,14S,17R)-17-hydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl] benzoate is not just a chemical entity; it holds potential that could lead to significant advancements in medical science and therapeutic applications.
Synonyms
alpha-Estradiol 3-benzoate
6045-53-0
Estra-1,3,5(10)-triene-3,17alpha-diol 3-benzoate
UNII-EB090UC9W9
EB090UC9W9
17.alpha.-Estradiol, 3-benzoate
EINECS 227-938-5
DTXSID90858951
.ALPHA.-ESTRADIOL 3-BENZOATE
[(8R,9S,13S,14S,17R)-17-hydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl] benzoate
a-Estradiol 3-Benzoate
Estra-1,3,5(10)-triene-3,17-diol, 3-benzoate, (17.alpha.)-
ESTRADIOL BENZOATE IMPURITY E [EP IMPURITY]
3-BENZOYLOXY-17.ALPHA.-HYDROXYOESTRA-1,3,5(10)-TRIENE
17alpha-Hydroxyestra-1,3,5(10)-trien-3-yl Benzoate (17-epi-Estradiol Benzoate)
ESTRADIOL BENZOATE IMPURITY E (EP IMPURITY)
17alpha-Hydroxyestra-1,3,5(10)-trien-3-yl Benzoate; Estradiol Benzoate Imp. E (EP); 17-epi-Estradiol Benzoate; Estradiol Benzoate Impurity E
SCHEMBL301616
DTXCID501324365
AKOS025402169
17ALPHA-ESTRADIOL, 3-BENZOATE
AC-6013
NS00081191
Q27277079
3-BENZOYLOXY-17ALPHA-HYDROXYOESTRA-1,3,5(10)-TRIENE
ESTRA-1,3,5(10)-TRIENE-3,17-DIOL, 3-BENZOATE, (17ALPHA)-
227-938-5
Solubility of [(8R,9S,13S,14S,17R)-17-hydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl] benzoate
The solubility of the compound with the formula C26H34O3 can be quite intriguing. This complex structure indicates potential variations in solubility based on several factors:
This particular compound, featuring a benzoate group, may be expected to be more soluble in organic solvents due to its hydrophobic characteristics. However, it might show limited solubility in water due to the lack of strong ionic or polar interactions.
In conclusion, understanding the solubility behavior requires careful consideration of the compound's structure, the properties of the solvent, and the environmental conditions. As noted, "the context of solubility is as essential as the compound itself," shaping its potential applications and interactions.