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Catalog Number:
26459
CAS Number:
815619-80-8
Chlorhydrate d'ester allylique de N α -Fmoc-L-lysine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-L-Lys-OAll·HCl
Documents
$79.22 /250 mg
Taille
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Informations sur le produit

Na-Fmoc-L-lysine allyl ester hydrochloride is a versatile amino acid derivative widely utilized in peptide synthesis and bioconjugation applications. This compound features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which allows for selective deprotection during the synthesis process, making it an essential building block for researchers in the fields of medicinal chemistry and biochemistry. Its allyl ester functionality enhances its reactivity, facilitating the formation of peptide bonds and enabling the incorporation of lysine into complex peptide sequences.

This compound is particularly valuable in the development of peptide-based therapeutics, where precise control over amino acid sequences is crucial. Additionally, Na-Fmoc-L-lysine allyl ester hydrochloride can be employed in the synthesis of modified peptides for drug delivery systems, offering potential advantages in targeted therapy. Researchers appreciate its stability and ease of handling, which contribute to efficient synthesis workflows. With its unique properties, this compound stands out as an indispensable tool for professionals aiming to innovate in peptide chemistry and related fields.

Numéro CAS 
815619-80-8
Formule moléculaire
C24H28N2O4 · HCl
Poids moléculaire 
444.96
Rotation optique 
C24H28N2O4 · HCl
Informations générales
Numéro CAS 
815619-80-8
Formule moléculaire
C24H28N2O4 · HCl
Poids moléculaire 
444.96
Rotation optique 
C24H28N2O4 · HCl
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

Na-Fmoc-L-lysine allyl ester hydrochloride is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, enabling researchers to create complex structures for studying biological functions and interactions.
  • Drug Development: Its role in medicinal chemistry allows for the modification of drug candidates, enhancing their efficacy and bioavailability, which is crucial in developing new therapeutics.
  • Bioconjugation: The allyl ester functionality facilitates bioconjugation processes, making it valuable in creating targeted drug delivery systems and improving the specificity of treatments.
  • Protein Engineering: Researchers use this compound to introduce lysine residues into proteins, aiding in the study of protein structure and function, which is essential in biotechnology applications.
  • Research in Cancer Therapy: Its applications extend to cancer research, where it helps in the design of peptide-based inhibitors that can selectively target cancer cells, offering potential advancements in treatment strategies.

Citations