Estrone
ADVERTISEMENT
- Molecular formula
- C18H22O2
- CAS Number
- 53-16-7
- IUPAC Name
- (8R,9S,10R,13S,14S,17S)-17-hydroxy-10,13,17-trimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-one
- Molecular Weight
- 270.37g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2300g/cm3
- Synonyms
- methyltestosterone
Identification
Interesting facts
Exploring the Compound: (8R,9S,10R,13S,14S,17S)-17-Hydroxy-10,13,17-trimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-one
This compound is a fascinating member of the steroid family, notable for its complex and stereospecific structure that contributes significantly to its biological activity. As you delve into the study of this compound, here are some intriguing aspects to consider:
- Stereochemistry: This compound features multiple stereocenters, indicated by its detailed stereochemical descriptors (8R, 9S, 10R, etc.). Understanding the spatial arrangement of these atoms is crucial, as it often dictates the compound's behavior in biological systems.
- Natural Occurrence: Compounds with similar structures can be found in various biological systems, where they may serve as hormones or signaling molecules, exemplifying the profound connection between chemistry and life.
- Applications: The unique properties of this compound suggest potential applications in pharmaceuticals, particularly in areas involving hormonal regulation or therapeutic targets in treating specific diseases.
- Mechanism of Action: Studying how such compounds interact with biological receptors can unravel mechanisms that are critical in medicinal chemistry, potentially leading to the development of new drugs.
As you continue your exploration of this compound, remember that every detail contributes to the bigger picture of how chemistry influences not only materials but also the very fabric of life itself. The intricate interplay between structure and function is what makes the study of compounds like this one both challenging and rewarding.