Ethenimose
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- Molecular formula
- C10H13Cl2N1O3S
- CAS Number
- 51-94-9
- IUPAC Name
- N-[4-[bis(2-chloroethyl)sulfamoyl]phenyl]acetamide
- Molecular Weight
- 271.16g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.8030g/cm3
- Synonyms
- ACETANILIDE, 4'-(BIS(2-CHLOROETHYL)SULFAMOYL)-
Identification
Interesting facts
Interesting Facts about N-[4-[bis(2-chloroethyl)sulfamoyl]phenyl]acetamide
N-[4-[bis(2-chloroethyl)sulfamoyl]phenyl]acetamide, often referred to by its shortened name, is a fascinating compound that has garnered attention in the field of medicinal chemistry due to its potential applications. Here are some remarkable insights into this compound:
- Anticancer Properties: This compound is explored as a potential chemotherapeutic agent. Its structure allows for interactions that may help in targeting cancer cells effectively.
- Mechanism of Action: The sulfamoyl functional group is important in its mechanism of action. It may inhibit enzymes such as carbonic anhydrase and has shown to interfere with the proliferation of specific tumor types.
- Biochemical Interactions: The presence of bis(2-chloroethyl) moiety suggests that this compound can undergo nucleophilic substitution reactions, which are typical in many anticancer agents.
- Drug Development: As researchers explore compounds like this, they focus on improving bioavailability and reducing toxicity, leading to the development of safer and more effective drugs.
- Structure-Activity Relationship (SAR): The design of this compound highlights the importance of its functional groups. Enhancing or modifying parts of its structure could lead to variations with improved efficacy and reduced side effects.
Overall, N-[4-[bis(2-chloroethyl)sulfamoyl]phenyl]acetamide showcases the intricate relationship between chemical structure and biological activity, which is a focal point of study in drug discovery. Keep an eye on this compound as research continues, and it may lead to breakthroughs in therapeutic interventions!