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Catalog Number:
03818
CAS Number:
20866-56-2
Ester N- hydroxysuccinimide de boc-L-tyrosine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-L-Tyr-OSu
Documents
$29.34 /1G
Taille
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Informations sur le produit

Boc-L-tyrosine N-hydroxysuccinimide ester is a versatile compound widely utilized in peptide synthesis and bioconjugation applications. This derivative of L-tyrosine features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and reactivity, making it an ideal choice for researchers looking to incorporate tyrosine into peptides or proteins without compromising their integrity. The N-hydroxysuccinimide (NHS) moiety facilitates efficient coupling reactions, allowing for the formation of stable amide bonds with various nucleophiles, including amino acids and proteins.

This compound is particularly valuable in the fields of drug development and biomolecular research, where precise modifications of peptides are essential for creating therapeutic agents or studying protein interactions. Its ability to selectively react with amines while maintaining the integrity of the tyrosine side chain opens up numerous possibilities for designing novel biomolecules. Researchers appreciate its ease of use and the high yield of reactions, making Boc-L-tyrosine N-hydroxysuccinimide ester a preferred choice for advancing peptide chemistry.

Numéro CAS 
20866-56-2
Formule moléculaire
C18H22N2O7
Poids moléculaire 
378.4
Rotation optique 
-13±1° (c= 1% dioxane)
Informations générales
Numéro CAS 
20866-56-2
Formule moléculaire
C18H22N2O7
Poids moléculaire 
378.4
Rotation optique 
-13±1° (c= 1% dioxane)
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

Boc-L-tyrosine N-hydroxysuccinimide ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures with specific functionalities, enhancing the development of therapeutic agents.
  • Drug Development: Its ability to modify amino acids makes it valuable in drug design, particularly in creating prodrugs that improve the bioavailability of active pharmaceutical ingredients.
  • Bioconjugation: The ester functionality facilitates the conjugation of biomolecules, which is crucial in developing targeted drug delivery systems and diagnostic tools in the biomedical field.
  • Research in Neuroscience: As a derivative of tyrosine, it plays a role in studying neurotransmitter pathways, aiding in the understanding of various neurological conditions and potential treatments.
  • Protein Engineering: It is used to introduce specific modifications in proteins, enhancing their stability and activity, which is essential for various applications in biotechnology and pharmaceuticals.

Citations