Sulinamid

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Identification

Molecular formula
C18H17NO4S
CAS Number
680-39-7
IUPAC Name
2-[4-(2-naphthylsulfonylamino)phenyl]ethanehydroxamic acid
Molecular Weight
377.44g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3560g/cm3
Synonyms
HDInhib_000022
Interesting facts

Interesting Facts about 2-[4-(2-naphthylsulfonylamino)phenyl]ethanehydroxamic acid

This fascinating compound, 2-[4-(2-naphthylsulfonylamino)phenyl]ethanehydroxamic acid, showcases a unique combination of functional groups that contributes to its biological significance. It is a synthetic derivative that has piqued the interest of chemists due to its potential therapeutic applications.

Here are some key highlights:

  • Anticancer Potential: Research has indicated that compounds related to hydroxamic acids can inhibit histone deacetylases (HDACs), a family of enzymes known to play a critical role in cancer progression.
  • Sulfonamide Group: The sulfonylamino moiety in this compound enhances its ability to interact with biological targets, providing important insights into drug design.
  • Structure-Activity Relationship (SAR): The intricate architecture of this compound, including the naphthalene and phenyl rings, lends itself well to studies aimed at expanding our understanding of how structural modifications can influence activity.

Interestingly, the hydroxamic acid functional group is renowned for its ability to chelate metal ions, which is not only valuable for therapeutic agents but also for applications in biochemistry and environmental science.

In summary, 2-[4-(2-naphthylsulfonylamino)phenyl]ethanehydroxamic acid is more than just a compound; it embodies the depth and complexity of organic chemistry, sparking curiosity for future research and applications. As scientists continue to explore its properties, we can expect to uncover even more about its potential in various fields, including medicinal chemistry and drug development.

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