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Catalog Number:
06545
CAS Number:
201048-68-2
- Z - - Fmoc-L-ornithine
Purity:
≥ 98 % (HPLC)
Synonym(s):
ZL-Orn(Fmoc)-OH
Documents
$113.87 /1G
Taille
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Informations sur le produit

Na-Z-Nd-Fmoc-L-ornithine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which is crucial for the selective protection of amino groups during the synthesis of complex peptides. Its unique structure allows for enhanced stability and solubility, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry.

In practical applications, Na-Z-Nd-Fmoc-L-ornithine serves as a key building block in the synthesis of bioactive peptides, which can be used in therapeutic agents targeting various diseases. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of the amino acid sequence is particularly advantageous in the development of peptide-based drugs. Additionally, this compound is recognized for its potential in the creation of novel drug delivery systems, enhancing the efficacy and specificity of therapeutic compounds.

Numéro CAS 
201048-68-2
Formule moléculaire
C28H28N2O6
Poids moléculaire 
488.55
Point de fusion 
96 - 99 °C
Rotation optique 
[a] 20 D = -2 ± 1 º (C=1 dans DMF)
Informations générales
Numéro CAS 
201048-68-2
Formule moléculaire
C28H28N2O6
Poids moléculaire 
488.55
Point de fusion 
96 - 99 °C
Rotation optique 
[a] 20 D = -2 ± 1 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-Z-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 therapeutic agents and vaccines.
  • Drug Development: Its unique structure allows for the creation of modified peptides that can enhance drug efficacy and specificity, making it valuable in pharmaceutical research.
  • Bioconjugation: The chemical is used in bioconjugation processes to attach biomolecules to drugs, improving delivery systems and targeting capabilities in cancer therapies.
  • Research in Neuroscience: It plays a role in studying neuropeptides, contributing to our understanding of neurological disorders and potential treatments.
  • Cosmetic Formulations: The compound is also explored in cosmetic chemistry for its potential benefits in skin care products, particularly in anti-aging formulations.

Citations