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Catalog Number:
29706
CAS Number:
1097192-04-5
N a -Fmoc-N d -azido-L-ornithine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Acide ( S )-5-azido-2-(Fmoc-amino)pentanoïque, Fmoc-5-azido-L-norvaline
Documents
$70.50 /100 mg
Taille
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Informations sur le produit

Na-Fmoc-Nd-azido-L-ornithine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and bioconjugation applications. This compound features a unique azido group, which allows for selective reactions in click chemistry, making it an invaluable tool for researchers in the fields of medicinal chemistry and biochemistry. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group facilitates easy incorporation into peptides, enabling the synthesis of complex structures with high purity and yield.

This compound is particularly beneficial for the development of peptide-based therapeutics and probes, as it can be utilized in the creation of bioactive molecules with enhanced stability and specificity. The azido functionality opens avenues for further modifications, such as the attachment of various biomolecules or labels, thus expanding its application in drug discovery and diagnostic development. Researchers will appreciate its compatibility with standard solid-phase peptide synthesis techniques, making it a reliable choice for innovative projects in peptide chemistry.

Numéro CAS 
1097192-04-5
Formule moléculaire
C20H20N4O4
Poids moléculaire 
380.4
Point de fusion 
132 - 140 ºC (lit.)
Rotation optique 
[a] D 20 = -13,5 à -15,5 º (C = 1 dans DMF)
Informations générales
Numéro CAS 
1097192-04-5
Formule moléculaire
C20H20N4O4
Poids moléculaire 
380.4
Point de fusion 
132 - 140 ºC (lit.)
Rotation optique 
[a] D 20 = -13,5 à -15,5 º (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-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 compounds and pharmaceuticals.
  • Drug Development: It plays a crucial role in medicinal chemistry, aiding researchers in creating novel therapeutic agents with enhanced efficacy and specificity.
  • Bioconjugation: The azido group allows for click chemistry applications, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in drug delivery systems.
  • Protein Engineering: This chemical is used in modifying proteins to study their functions and interactions, contributing to advancements in biotechnology and molecular biology.
  • Research in Cancer Therapeutics: Its applications extend to cancer research, where it helps in designing targeted therapies that can selectively attack cancer cells, improving treatment outcomes.

Citations