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Catalog Number:
33493
CAS Number:
1584133-25-4
N α -Fmoc- N ε -(propargyloxy)carbonyl-L-lysine
Purity:
≥ 99 % (dosage par titration, HPLC)
Synonym(s):
Fmoc-L-Lys(Poc)-OH, Nα -Fmoc- Nε- (prop-2-ynyloxycarbonyl)-L-lysine
Documents
$58.69 /100 mg
Taille
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Informations sur le produit

Na-Fmoc-Ne-(propargyloxy)carbonyl-L-lysine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc group, which is essential for the selective deprotection of amino acids during solid-phase peptide synthesis (SPPS). Its unique propargyloxycarbonyl group enhances its reactivity, making it an ideal candidate for applications in click chemistry, particularly in the synthesis of complex peptides and bioconjugates. Researchers appreciate its ability to facilitate the introduction of functional groups, allowing for the creation of diverse molecular architectures.

In addition to its role in peptide synthesis, Na-Fmoc-Ne-(propargyloxy)carbonyl-L-lysine is valuable in the development of therapeutics, particularly in the field of cancer research and drug delivery systems. Its stability and compatibility with various coupling reagents make it a preferred choice for chemists looking to streamline their synthesis processes. The compound's unique properties not only enhance the efficiency of peptide assembly but also open avenues for innovative applications in medicinal chemistry and biochemistry.

Numéro CAS 
1584133-25-4
Formule moléculaire
C25H26N2O6
Poids moléculaire 
450.5
Rotation optique 
[a] 20 D
Informations générales
Numéro CAS 
1584133-25-4
Formule moléculaire
C25H26N2O6
Poids moléculaire 
450.5
Rotation optique 
[a] 20 D
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

Na -Fmoc- Ne -(propargyloxy)carbonyl-L-lysine 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 for drug development and biological studies.
  • Bioconjugation: It is used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, enhancing the functionality of diagnostic tools and therapeutic agents.
  • Drug Delivery Systems: The compound can be incorporated into drug delivery systems, improving the targeting and release profiles of pharmaceuticals, which is crucial in cancer therapy and other treatments.
  • Research in Neuroscience: It plays a role in neuroscience research by facilitating the study of protein interactions and signaling pathways, contributing to a better understanding of neurological diseases.
  • Development of Therapeutic Agents: Its unique properties enable the design of novel therapeutic agents, particularly in the field of personalized medicine, where tailored treatments are essential for patient care.

Citations