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Catalog Number:
30528
CAS Number:
1176270-25-9
N α -Fmoc-N δ -Azido-D-Ornithine
Purity:
99% (HPLC)
Synonym(s):
Acide ( R )-Fmoc-2-amino-5-azido-pentanoïque, Fmoc-D-Orn(N3)-OH
Documents
$113.87 /100 mg
Taille
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Informations sur le produit

Na-Fmoc-Nd-Azido-D-Ornithine is a specialized amino acid derivative that plays a pivotal role in peptide synthesis and bioconjugation applications. This compound is particularly valued in the field of medicinal chemistry and drug development due to its unique azide functional group, which allows for efficient click chemistry reactions. Researchers utilize Na-Fmoc-Nd-Azido-D-Ornithine to create complex peptide structures that can be employed in the development of targeted therapies and novel biomaterials. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group facilitates easy incorporation into peptide chains, making it an essential tool for chemists focused on synthesizing peptides with specific functionalities.

The compound's azido group not only enhances its reactivity but also provides opportunities for further modifications, enabling the creation of diverse conjugates for applications in diagnostics and therapeutics. With its ability to streamline the synthesis of bioactive peptides, Na-Fmoc-Nd-Azido-D-Ornithine stands out as a valuable asset for researchers aiming to innovate in the fields of drug discovery and biomolecular engineering.

Numéro CAS 
1176270-25-9
Formule moléculaire
C20H20N4O4
Poids moléculaire 
380.4
Point de fusion 
132 - 140 °C
Rotation optique 
[a] D 20 = 13,5 - 15,5 ° (C = 1 dans DMF)
Informations générales
Numéro CAS 
1176270-25-9
Formule moléculaire
C20H20N4O4
Poids moléculaire 
380.4
Point de fusion 
132 - 140 °C
Rotation optique 
[a] D 20 = 13,5 - 15,5 ° (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-Fmoc-Nd-Azido-D-Ornithine is widely utilized in research focused on:

  • Peptide Synthesis: This compound is crucial for the development of peptides in medicinal chemistry, allowing researchers to create complex structures with specific functionalities.
  • Drug Development: Its azido group enables click chemistry applications, facilitating the attachment of drug molecules to targeting agents, which enhances therapeutic efficacy.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps in linking biomolecules, such as proteins and antibodies, to improve drug delivery systems.
  • Research in Neuroscience: It plays a role in studying neuropeptides, contributing to the understanding of neurological pathways and potential treatments for neurodegenerative diseases.
  • Custom Synthesis: Researchers benefit from its versatility in creating tailored compounds for specific biological assays, making it a valuable tool in pharmaceutical research.

Citations