Découvrez le nouveau Chem-Impex : là où l'innovation commence par une liaison.

Catalog Number:
04994
CAS Number:
147290-11-7
N α -Fmoc- N δ -allyloxycarbonyl-L-ornithine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Orn(Aloc)-OH
Documents
$35.00 /1G
Taille
Request Bulk Quote
Informations sur le produit

Na-Fmoc-Nd-allyloxycarbonyl-L-ornithine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is widely recognized for its stability and ease of removal under mild conditions, making it an ideal choice for solid-phase peptide synthesis. The allyloxycarbonyl group enhances its reactivity, allowing for selective modifications that are essential in the design of bioactive peptides. Researchers and industry professionals utilize this compound in the development of therapeutics, particularly in the fields of oncology and immunology, where precise peptide structures are critical for efficacy.

The unique properties of Na-Fmoc-Nd-allyloxycarbonyl-L-ornithine enable it to serve as a building block for complex peptide sequences, facilitating the exploration of novel drug candidates. Its compatibility with various coupling reagents and its ability to undergo further functionalization make it a valuable tool in medicinal chemistry. By incorporating this compound into their workflows, researchers can streamline the synthesis of peptides with enhanced biological activity and specificity, ultimately contributing to advancements in drug discovery and development.

Numéro CAS 
147290-11-7
Formule moléculaire
C24H26N2O6
Poids moléculaire 
438.5
Point de fusion 
106 - 118 °C
Rotation optique 
[a] D 20 = -8,5 ± 2 º (C = 1 dans DMF)
Informations générales
Numéro CAS 
147290-11-7
Formule moléculaire
C24H26N2O6
Poids moléculaire 
438.5
Point de fusion 
106 - 118 °C
Rotation optique 
[a] D 20 = -8,5 ± 2 º (C = 1 dans DMF)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

Na-Fmoc-Nd-allyloxycarbonyl-L-ornithine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the creation of complex peptide structures with high purity.
  • Drug Development: Its unique functional groups make it valuable in the development of novel pharmaceuticals, especially in creating targeted therapies that require specific amino acid sequences.
  • Bioconjugation: The compound is used in bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is crucial in developing biosensors and drug delivery systems.
  • Research in Protein Engineering: It plays a significant role in protein engineering, aiding researchers in modifying proteins to enhance their stability and functionality, which is essential in various biotechnological applications.
  • Cosmetic Formulations: The compound finds applications in cosmetic chemistry, particularly in formulations aimed at skin rejuvenation, where its properties can enhance the delivery of active ingredients.

Citations