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Catalog Number:
30517
CAS Number:
1994267-98-9
N α -Azido-N δ -Fmoc-L-Ornithine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Acide ( S )-2-azido-5-(Fmoc-amino)pentanoïque, N3-L-Orn(Fmoc)-OH
Documents
$58.39 /100 mg
Taille
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Informations sur le produit

Na-Azido-Nd-Fmoc-L-Ornithine is a versatile compound widely utilized in peptide synthesis and bioconjugation applications. This amino acid derivative features an azido group, which allows for efficient click chemistry reactions, making it an excellent choice for researchers looking to create complex biomolecules. The Fmoc (9-fluorenylmethoxycarbonyl) protecting group provides stability during synthesis, facilitating the production of peptides with high purity and yield. Its unique structure enables the incorporation of azido functionalities into peptides, which can be further modified for targeted drug delivery systems or in the development of novel therapeutic agents.

In addition to its role in peptide synthesis, Na-Azido-Nd-Fmoc-L-Ornithine is increasingly being explored in the field of materials science for the development of functionalized surfaces and nanomaterials. Its ability to participate in bioorthogonal reactions makes it a valuable tool for researchers aiming to study protein interactions and cellular processes. With its combination of stability, reactivity, and versatility, this compound is an essential addition to the toolkit of any professional working in chemical biology or medicinal chemistry.

Numéro CAS 
1994267-98-9
Formule moléculaire
C20H20N4O4
Poids moléculaire 
380.4
Point de fusion 
78-87 °C
Rotation optique 
[a] D 20 = - 30 ± 2º (C = 1 dans DMF)
Informations générales
Numéro CAS 
1994267-98-9
Formule moléculaire
C20H20N4O4
Poids moléculaire 
380.4
Point de fusion 
78-87 °C
Rotation optique 
[a] D 20 = - 30 ± 2º (C = 1 dans DMF)
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-Azido-Nd-Fmoc-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 the development of bioactive peptides that can be used in pharmaceuticals.
  • Drug Development: Its unique azido group allows for click chemistry applications, facilitating the creation of complex drug molecules that can target specific biological pathways.
  • Bioconjugation: The azido functionality enables efficient bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules for enhanced therapeutic effects.
  • Research in Cancer Therapy: By incorporating this compound into therapeutic agents, researchers can explore targeted delivery systems that improve the efficacy of cancer treatments while minimizing side effects.
  • Material Science: It is also applied in the development of smart materials that respond to environmental stimuli, thanks to its functional groups that can be modified for various applications.

Citations