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Catalog Number:
06333
CAS Number:
160446-35-5
N -1-Trityl-désamino-histidine
Purity:
≥ 98 % (dosage)
Synonym(s):
Acide 3-( N -1-trityl-imidazol-4-yl)propionique, Acide N -1-trityl-dihydrourocanique
Documents
$149.02 /250 mg
Taille
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Informations sur le produit

N-1-Trityl-deamino-histidine is a versatile compound widely recognized for its applications in peptide synthesis and pharmaceutical research. This derivative of histidine features a trityl protecting group, which enhances its stability and solubility, making it an ideal choice for researchers engaged in the development of biologically active peptides. Its unique structure allows for selective deprotection, facilitating the synthesis of complex molecules with precision.

In the pharmaceutical industry, N-1-Trityl-deamino-histidine is particularly valuable in the design of drug candidates that target specific biological pathways. Its ability to mimic natural amino acids while providing enhanced stability opens up possibilities for creating more effective therapeutic agents. Additionally, this compound can be utilized in various biochemical assays, contributing to advancements in drug discovery and development. Researchers appreciate its reliability and efficiency in producing high-purity peptides, which are crucial for both academic studies and industrial applications.

Numéro CAS 
160446-35-5
Formule moléculaire
C25H22N2O2
Poids moléculaire 
382.48
Informations générales
Numéro CAS 
160446-35-5
Formule moléculaire
C25H22N2O2
Poids moléculaire 
382.48
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

N-1-Trityl-deamino-histidine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of therapeutic proteins. Its stability and reactivity make it ideal for creating complex structures.
  • Drug Development: It plays a significant role in pharmaceutical research, especially in designing new drugs that target specific biological pathways. Researchers appreciate its ability to enhance the bioavailability of active compounds.
  • Bioconjugation: The compound is used in bioconjugation processes, allowing for the attachment of drugs or imaging agents to proteins. This application is crucial in targeted therapy and diagnostic imaging.
  • Research in Cancer Therapies: Its unique properties make it valuable in developing cancer treatments, where it can help improve the selectivity and efficacy of anticancer agents.
  • Protein Engineering: N-1-Trityl-deamino-histidine is utilized in protein engineering to modify protein functions, enhancing their stability and activity for various industrial applications.

Citations