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Catalog Number:
05512
CAS Number:
16937-92-1
N α -Boc- N δ -ZD-ornithine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc-D-Orn(Z)-OH
Documents
$22.03 /1G
Taille
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Informations sur le produit

Na-Boc-Nd-Z-D-ornithine is a valuable derivative of ornithine, widely recognized for its applications in peptide synthesis and drug development. This compound features a tert-butoxycarbonyl (Boc) protecting group, which enhances its stability and reactivity, making it an ideal choice for researchers engaged in the synthesis of complex peptides. Its unique structure allows for selective reactions, facilitating the incorporation of ornithine into peptide chains, which is crucial in the design of bioactive compounds, including pharmaceuticals and therapeutic agents.

In addition to its role in peptide synthesis, Na-Boc-Nd-Z-D-ornithine has shown potential in the development of novel drug candidates targeting various biological pathways. Researchers appreciate its compatibility with standard coupling reagents and its ability to improve the solubility of peptides, thereby enhancing their bioavailability. This compound is particularly beneficial in the fields of medicinal chemistry and biochemistry, where precision and efficiency in synthesis are paramount. With its robust profile, Na-Boc-Nd-Z-D-ornithine stands out as a key reagent for advancing peptide-based research and applications.

Numéro CAS 
16937-92-1
Formule moléculaire
C18H26N2O6
Poids moléculaire 
366.42
Point de fusion 
84-95 °C
Rotation optique 
[α] D 20 = +3 ± 2º (C=1 dans AcOH)
Informations générales
Numéro CAS 
16937-92-1
Formule moléculaire
C18H26N2O6
Poids moléculaire 
366.42
Point de fusion 
84-95 °C
Rotation optique 
[α] D 20 = +3 ± 2º (C=1 dans AcOH)
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-Boc-Nd-Z-D-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 therapeutic agents. Its protective groups allow for selective reactions, enhancing yield and purity.
  • Drug Development: In pharmaceutical research, it is used to create novel drug candidates targeting various diseases, including cancer and metabolic disorders, due to its structural versatility.
  • Bioconjugation: The compound is effective in bioconjugation processes, allowing researchers to attach biomolecules to drugs or imaging agents, improving specificity and efficacy in targeted therapies.
  • Protein Engineering: It plays a significant role in modifying proteins to enhance their stability and functionality, which is crucial in biotechnology applications and enzyme design.
  • Research in Neuroscience: This compound is explored in studies related to neuropeptides, aiding in the understanding of neurological pathways and potential treatments for neurodegenerative diseases.

Citations