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Catalog Number:
06162
CAS Number:
33173-53-4
4-Azido-L-phénylalanine
Purity:
≥ 99,9 % (HPLC chirale)
Synonym(s):
L-Phe(4-azido)-OH, p-Azido-L-phénylalanine
Documents
$77.32 /100 mg
Taille
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Informations sur le produit

4-Azido-L-phenylalanine is a versatile amino acid derivative that has gained significant attention in the fields of biochemistry and molecular biology. This compound, characterized by its unique azido group, serves as a powerful tool for bioconjugation and labeling applications. Researchers utilize 4-Azido-L-phenylalanine to incorporate azide functionalities into proteins and peptides, facilitating the study of protein interactions and dynamics. Its ability to undergo click chemistry reactions makes it particularly valuable for creating complex biomolecular structures, enhancing the understanding of cellular processes.

In addition to its applications in protein engineering, 4-Azido-L-phenylalanine is also explored in drug development and delivery systems. The azido group allows for selective modification of therapeutic agents, potentially improving their efficacy and targeting capabilities. With its unique properties and diverse applications, 4-Azido-L-phenylalanine stands out as an essential compound for researchers aiming to innovate in the fields of biotechnology and pharmaceuticals.

Numéro CAS 
33173-53-4
Formule moléculaire
C9H10N4O2
Poids moléculaire 
206.1
Informations générales
Numéro CAS 
33173-53-4
Formule moléculaire
C9H10N4O2
Poids moléculaire 
206.1
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

4-Azido-L-phenylalanine is widely utilized in research focused on:

  • Bioconjugation: This compound is often used in bioconjugation techniques to attach biomolecules to surfaces or other molecules, enhancing the development of targeted drug delivery systems.
  • Protein Labeling: Researchers employ 4-Azido-L-phenylalanine for the site-specific labeling of proteins, allowing for better tracking and analysis of protein interactions in cellular studies.
  • Photochemistry: Its azido group can undergo photochemical reactions, making it valuable in creating light-responsive materials and in studies involving photo-crosslinking.
  • Drug Development: The compound is explored in the synthesis of novel pharmaceuticals, particularly in creating compounds that can selectively target specific cells or tissues.
  • Research in Neuroscience: It is used in studies related to neurotransmitter pathways, helping to understand the role of amino acids in brain function and potential therapeutic targets.

Citations