Celecoxib
- Molecular formula
- C17H14ClN3O2S
- CAS Number
- 169590-42-5
- IUPAC Name
- 5-chloro-N-[2-[4-(cyclohexylcarbamoylsulfamoyl)phenyl]ethyl]-2-methoxy-benzamide
- Molecular Weight
- 381.38g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4040g/cm3
- Synonyms
- glyburide
Identification
Interesting Facts about 5-Chloro-N-[2-[4-(Cyclohexylcarbamoylsulfamoyl)phenyl]ethyl]-2-methoxy-benzamide
This compound is a member of the benzamide family, a class of compounds known for their diverse biological activities. As an advanced organic molecule, it incorporates a variety of functional groups that contribute to its unique properties and potential applications.
Key Features
- Anti-inflammatory Properties: Many compounds within the benzamide category, particularly those with sulfamoyl groups, exhibit significant anti-inflammatory effects, making them promising candidates for treating various inflammatory diseases.
- Complex Structure: This molecule’s structure includes a chlorobenzene moiety, a methoxy group, and a cyclohexylcarbamoyl moiety, which all enhance its biological activity and hydrophobic character.
- Cyclohexylcarbamoylsulfamoyl Group: The inclusion of this group is particularly interesting, as it can influence the binding affinity and selectivity towards biological targets, such as enzymes or receptors.
Moreover, research suggests that compounds like this can interfere with key biological pathways, potentially allowing for innovations in medicinal chemistry. The development of similar compounds has led to new therapeutics for diseases such as cancer and autoimmune disorders.
Quote from a Chemist
"The precise arrangement of atoms in complex molecules like this one holds the key to unlocking new therapeutic avenues. Each element plays a crucial role in its overall behavior." - A Chemistry Researcher
In summary, the intricate structure and potential biological applications of 5-chloro-N-[2-[4-(cyclohexylcarbamoylsulfamoyl)phenyl]ethyl]-2-methoxy-benzamide make it a fascinating subject of study in the world of pharmaceutical research.