Interesting facts
Interesting Facts About (8R,9S,10R,13S,14S,17R)-17-acetyl-17-hydroxy-6,10,13-trimethyl-2,8,9,11,12,14,15,16-octahydro-1H-cyclopenta[a]phenanthren-3-one
This compound, a steroid-derived substance, presents a fascinating combination of structure and potential applications in various fields including pharmacology and biochemistry. Here are some intriguing aspects:
- Steroidal Framework: The compound belongs to a class of molecules that are structurally related to steroids, which are vital in biochemical processes including hormonal function.
- Natural Occurrence: Steroid compounds like this one can be found in various plants and animals, playing crucial roles in metabolism and regulatory functions.
- Biological Activity: The functional groups (acetyl and hydroxy) suggest potential biological activity, making it a subject of interest for drug development and therapeutic applications.
- Stereochemistry: With multiple stereocenters, this compound exhibits chirality, which can affect its biological interactions. The specific stereochemical configuration may lead to diverse biological effects.
As stated by prominent chemists, “The shape of a molecule determines its function.” Thus, the intricate structure of this octahydro-cyclopenta compound may influence its binding affinity to biological targets.
Researchers continue to investigate similar compounds for their potential in treating diseases, especially in the realms of cancer and hormonal therapies, reflecting the ongoing importance of natural products in developing innovative pharmaceutical solutions.
Synonyms
megestrol
3562-63-8
Megestrolo
Pregna-4,6-diene-3,20-dione, 17-hydroxy-6-methyl-
Chronopil
Megestrolum
17-Hydroxy-6-methylpregna-4,6-diene-3,20-dione
Megestrolum [INN-Latin]
HSDB 3233
UNII-EA6LD1M70M
EINECS 222-628-6
EA6LD1M70M
CHEBI:6722
DTXSID001009330
Megestrolum (INN-Latin)
Compound 5071
G03AC05
G03DB02
L02AB01
DTXCID001436159
222-628-6
Megestrol (INN)
(8R,9S,10R,13S,14S,17R)-17-acetyl-17-hydroxy-6,10,13-trimethyl-2,8,9,11,12,14,15,16-octahydro-1H-cyclopenta[a]phenanthren-3-one
(8R,9S,10R,13S,14S,17R)-17-Acetyl-17-hydroxy-6,10,13-trimethyl-8,9,10,11,12,13,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3(2H)-one
MEGESTROL [INN]
Megestrol [INN:BAN]
Megestrol (Acetate)
Chronopil (TN)
Pregna-4,6-diene-3,20-dione, 17-hydroxy-6-methyl-; 17-Hydroxy-6-methylpregna-4,6-diene-3,20-dione; Megestrol; 6-Methyl-17-hydroxypregna-4,6-diene-3,20-dione
Megestrol (Standard)
MEGESTROL [HSDB]
MEGESTROL [VANDF]
MEGESTROL [WHO-DD]
SCHEMBL8942
GTPL9128
CHEMBL4071215
HY-B1834R
VXIMPSPISRVBPZ-NWUMPJBXSA-N
HY-B1834
s5738
FH39644
AC-32473
MS-25250
CS-0013903
NS00014345
C07120
D08167
MEGESTROL ACETATE IMPURITY B [EP IMPURITY]
Q410513
Solubility of (8R,9S,10R,13S,14S,17R)-17-acetyl-17-hydroxy-6,10,13-trimethyl-2,8,9,11,12,14,15,16-octahydro-1H-cyclopenta[a]phenanthren-3-one
The solubility of complex organic compounds like (8R,9S,10R,13S,14S,17R)-17-acetyl-17-hydroxy-6,10,13-trimethyl-2,8,9,11,12,14,15,16-octahydro-1H-cyclopenta[a]phenanthren-3-one can be influenced by various factors. Understanding its solubility characteristics is crucial for its application in pharmaceuticals and other fields. Here are some key points:
It is essential to conduct empirical experiments to establish precise solubility data, as theoretical predictions may not always align perfectly with reality. Therefore, a thorough understanding of the compound's solubility profile is vital for its effective use and formulation.