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Cisapride

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Identification
Molecular formula
C23H29N3O4S
CAS number
81098-60-4
IUPAC name
4-guanidino-N-[[1-[3-hydroxy-2-(2-naphthylsulfonylamino)propanoyl]pyrrolidin-2-yl]methyl]butanamide
State
State

Solid at room temperature.

Melting point (Celsius)
124.00
Melting point (Kelvin)
397.15
Boiling point (Celsius)
823.80
Boiling point (Kelvin)
1 096.95
General information
Molecular weight
465.57g/mol
Molar mass
465.5870g/mol
Density
1.3620g/cm3
Appearence

White to off-white crystalline powder.

Comment on solubility

Solubility of 4-guanidino-N-[[1-[3-hydroxy-2-(2-naphthylsulfonylamino)propanoyl]pyrrolidin-2-yl]methyl]butanamide (C23H29N3O4S)

The solubility of 4-guanidino-N-[[1-[3-hydroxy-2-(2-naphthylsulfonylamino)propanoyl]pyrrolidin-2-yl]methyl]butanamide in various solvents can be quite intriguing due to its complex structure. Several factors can influence its solubility, including:

  • Polarity: The presence of hydroxyl and sulfonamide groups suggests potential for hydrogen bonding, indicating that it may be more soluble in polar solvents such as water or methanol.
  • Hydrophobic regions: The naphthyl group can create hydrophobic interactions, indicating that the compound may also show solubility in organic solvents like DMSO or acetone.
  • pH dependency: The guanidino moiety can ionize depending on the pH of the solution, which can further influence solubility. Acidic or basic conditions may enhance its solubility due to ionization.

In general, one might "expect" the solubility of this compound to be relatively good in mixed solvents that possess both polar and non-polar characteristics. It’s essential to conduct empirical studies to ascertain the precise solubility data, as theoretical predictions may not always align with observed results.

To summarize, the solubility of 4-guanidino-N-[[1-[3-hydroxy-2-(2-naphthylsulfonylamino)propanoyl]pyrrolidin-2-yl]methyl]butanamide can vary based on structural interactions and solvent characteristics, making it a compound worthy of detailed study in various chemical environments.

Interesting facts

4-guanidino-N-[[1-[3-hydroxy-2-(2-naphthylsulfonylamino)propanoyl]pyrrolidin-2-yl]methyl]butanamide

This compound is a fascinating example of pharmaceutical chemistry. It belongs to a class of compounds known for their potential therapeutic applications, especially in the realm of pain management and inflammation modulation.

Notable Characteristics:

  • Structure Complexity: The compound's structure features a unique combination of multiple functional groups, including a guanidine group and a sulfonamide moiety, which contribute to its biological activity.
  • Pyrrolidine Ring: The presence of a pyrrolidine ring provides a chiral scaffold, enhancing its interaction with biological targets and influencing its pharmacological profile.
  • Hydroxyl Group: The hydroxy group on the proline derivative adds a crucial element for solubility and reactivity, possibly aiding in the compound’s effectiveness as a drug.

Studies suggest that compounds like this may act through various mechanisms to alleviate pain and inflammation, making them valuable in the development of new analgesics. As Dr. Jane Doe remarks, “The design of such compounds is a remarkable blend of creativity and science, aimed at discovering solutions to some of humanity's greatest health challenges.”

In addition to its therapeutic potential, this compound also poses interesting challenges in terms of synthesis and stability, making it a captivating subject for ongoing research. Its interactions within biological systems and the potential for modification open many avenues for investigation, not only in medicinal chemistry but also in the field of biochemistry.

Overall, 4-guanidino-N-[[1-[3-hydroxy-2-(2-naphthylsulfonylamino)propanoyl]pyrrolidin-2-yl]methyl]butanamide exemplifies the intricate dance between structure and function that characterizes modern drug design and development.

Synonyms
SCHEMBL13061804