Valine nitrotyrosine

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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
Molecular Weight
313.32g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.4900g/cm3
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.

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