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Catalog Number:
00826
CAS Number:
79950-65-5
Boc-His(3-Bom)-OH
Purity:
≥ 98,5 % (HPLC)
Synonym(s):
Boc-L-His(π-Bom)-OH, Boc- N - p -benzyloxyméthyl-L-histidine
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$25.20 /1G
Taille
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Informations sur le produit

Boc-His(3-Bom)-OH is a specialized amino acid derivative that plays a crucial role in peptide synthesis and bioconjugation applications. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal choice for researchers engaged in the development of peptide-based therapeutics and biomolecules. Its unique structure, characterized by the imidazole side chain, allows for specific interactions in biological systems, facilitating the design of targeted drug delivery systems and enzyme inhibitors.

In the pharmaceutical industry, Boc-His(3-Bom)-OH is utilized for the synthesis of histidine-containing peptides, which are essential in various biological processes, including enzyme catalysis and metal ion coordination. Additionally, its application extends to the development of diagnostic agents and in the field of proteomics, where it aids in the identification and characterization of proteins. Researchers benefit from its ease of use and compatibility with standard coupling reagents, making it a valuable tool in peptide chemistry and drug discovery.

Numéro CAS 
79950-65-5
Formule moléculaire
C19H25N3O5
Poids moléculaire 
375.43
Point de fusion 
146 - 152 °C
Rotation optique 
[a] D 20 = 6 ± 2 º (C = 1 dans MeOH)
Informations générales
Numéro CAS 
79950-65-5
Formule moléculaire
C19H25N3O5
Poids moléculaire 
375.43
Point de fusion 
146 - 152 °C
Rotation optique 
[a] D 20 = 6 ± 2 º (C = 1 dans MeOH)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Boc-His(3-Bom)-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly those that require protected histidine residues. Its stability under various reaction conditions makes it ideal for complex peptide chains.
  • Drug Development: In pharmaceutical research, it is used to develop novel therapeutic agents, especially in the field of cancer treatment, where histidine derivatives can play a role in targeting specific pathways.
  • Bioconjugation: The compound is valuable in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing the specificity and efficacy of drug delivery systems.
  • Protein Engineering: It aids in the modification of proteins to study their functions and interactions, providing insights into enzyme activity and protein stability, which is crucial for biotechnological applications.
  • Research in Immunology: The compound is used in the design of immunogenic peptides for vaccine development, helping to stimulate immune responses effectively and contributing to advancements in immunotherapy.

Citations