Skip to main content

Valine nitrotyrosine

ADVERTISEMENT
Identification
Molecular formula
C14H19N3O6
CAS number
4420-72-2
IUPAC name
2-[[3-amino-2-hydroxy-4-(4-nitrophenyl)butanoyl]amino]-4-methyl-pentanoic acid
State
State

At room temperature, valine nitrotyrosine is in a solid state, marked by its crystalline structure. Typically, it appears as a powder or crystalline solid.

Melting point (Celsius)
156.00
Melting point (Kelvin)
429.00
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.00
General information
Molecular weight
313.32g/mol
Molar mass
313.2930g/mol
Density
1.4900g/cm3
Appearence

Valine nitrotyrosine is typically a crystalline solid with a slightly yellow to off-white appearance. It can be observed as a powder or in crystalline chunks depending on its preparation and storage.

Comment on solubility

Solubility of 2-[[3-amino-2-hydroxy-4-(4-nitrophenyl)butanoyl]amino]-4-methyl-pentanoic acid

The solubility of the compound 2-[[3-amino-2-hydroxy-4-(4-nitrophenyl)butanoyl]amino]-4-methyl-pentanoic acid (C14H19N3O6) is influenced by various factors due to its complex structure. Understanding its solubility can be essential for applications in pharmaceuticals and biochemistry.

Key Factors Influencing Solubility:

  • Polarity: The presence of functional groups such as amino and hydroxy enhances polar interactions with solvents, facilitating solubility in polar solvents like water.
  • Hydrogen Bonding: This compound can engage in hydrogen bonding due to the hydroxyl (-OH) and amino (-NH2) groups, which can significantly increase solubility.
  • pH Sensitivity: As an acid, the solubility may vary with changes in pH, with potential increases in solubility at higher pH values due to deprotonation of the acid group.
  • Temperature: Generally, increased temperatures can enhance solubility for many compounds, including this one.

In conclusion, the solubility of this compound is likely to be moderate in aqueous solutions, and it may display enhanced solubility characteristics due to its ability to form hydrogen bonds and variations in pH. Understanding these aspects is crucial for predicting the behavior of this compound in biological systems or during synthesis.

Interesting facts

Interesting Facts about 2-[[3-amino-2-hydroxy-4-(4-nitrophenyl)butanoyl]amino]-4-methyl-pentanoic acid

This intriguing compound, often referred to in the scientific community as a peptide derivative, represents a unique structure that is rich in functional groups. Here are some fascinating aspects of this compound:

  • Biochemical Significance: Due to the presence of amino groups, this compound may play a vital role in biological processes, potentially serving as a substrate or inhibitor in enzymatic reactions.
  • Nitrophenyl Group: The inclusion of a 4-nitrophenyl moiety is particularly interesting, as it can enhance the compound's reactivity and may impact its interaction with biological targets, making it useful in drug design.
  • Hydroxyl Functionality: The hydroxyl group contributes to its polar characteristics, which can influence the compound's solubility and biological activity, allowing it to engage in hydrogen bonding with biomolecules.
  • Potential Therapeutic Uses: Compounds with similar structures have been investigated for various therapeutic applications, including their potential as anti-inflammatory agents or in cancer therapies.
  • Research Implications: Given its complex structure, ongoing research may unveil novel uses or derivatives of this compound that could lead to breakthroughs in medicinal chemistry.

As chemists continue to explore the vast landscape of compounds, entities like 2-[[3-amino-2-hydroxy-4-(4-nitrophenyl)butanoyl]amino]-4-methyl-pentanoic acid remind us of the intricate connections between structure and function in biological systems. Each component, from the amino acid backbone to the nitrophenyl substituent, works harmoniously to bestow unique properties upon the compound.