Atorvastatin
- Molecular formula
- C33H35FN2O5
- CAS Number
- 134523-00-5
- IUPAC Name
- 7-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4-(phenylcarbamoyl)pyrrol-1-yl]-3,5-dihydroxy-heptanoic acid
- Molecular Weight
- 558.64g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2000g/cm3
- Appearance
- can depend on how it's processed, but it typically has a fine crystalline texture.
- Synonyms
- Atorvastatin(Relative)
Identification
Interesting Facts about 7-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4-(phenylcarbamoyl)pyrrol-1-yl]-3,5-dihydroxy-heptanoic acid
This intriguing compound, known for its complex structure and diverse applications, presents a wealth of fascinating characteristics that captivate both chemists and biologists alike.
Pharmacological Significance
One of the standout features of this compound is its potential in medicinal chemistry. Its unique structure allows it to interact with biological systems in novel ways. Here are some key points:
- Anticancer Activity: Preliminary studies suggest that compounds like this one may possess anticancer properties, making them a subject of interest in tumor research.
- Targeted Treatment: With its complex targeting ability, it holds promise for selective interaction with certain types of cancer cells.
Chemical Structure Features
The intricate molecular architecture of this compound incorporates various functional groups that offer unique reactivity:
- Fluorine Atom: The presence of fluorine enhances bioactivity, potentially impacting the pharmacokinetics.
- Pyrrole Ring: This five-membered ring is notable for its stability and versatility in forming biological compounds.
- Multiple Hydroxy Groups: The dihydroxy structure suggests applications in areas such as antioxidant activities.
Research Interest
Chemists and biochemists are particularly interested in this compound due to its multi-functional capabilities. As researchers delve into the potential modifications of its structure, they may discover:
- New Derivatives: There is ample opportunity for synthesis of derivatives that could exhibit enhanced therapeutic efficacy or reduced side effects.
- Mechanism of Action: Understanding how this compound interacts at the molecular level can lead to breakthroughs in drug design.
In conclusion, the study of 7-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4-(phenylcarbamoyl)pyrrol-1-yl]-3,5-dihydroxy-heptanoic acid is a testament to the intricate interplay between chemistry and biology. With ongoing research, this compound could pave the way for groundbreaking treatments in pharmacology.