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Catalog Number:
26460
CAS Number:
1301706-41-1
- Fmoc- - palmitoyl-L-ornithine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Orn(palmitoyl)-OH
Documents
$58.39 /100 mg
Taille
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Informations sur le produit

Na-Fmoc-Nd-palmitoyl-L-ornithine is a versatile amino acid derivative that plays a significant role in peptide synthesis and drug development. This compound features a unique palmitoyl group, enhancing its lipophilicity and facilitating cellular uptake, making it particularly valuable in the formulation of lipid-based drug delivery systems. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for easy incorporation into peptide chains, providing researchers with a reliable tool for synthesizing complex peptides with improved stability and bioactivity.

This compound is widely utilized in the fields of biochemistry and pharmaceutical research, especially in the development of targeted therapies and vaccines. Its ability to enhance the solubility and permeability of peptides makes it an attractive option for formulating therapeutic agents aimed at treating various diseases. Additionally, Na-Fmoc-Nd-palmitoyl-L-ornithine can be employed in the creation of novel biomaterials, contributing to advancements in drug delivery technologies and regenerative medicine.

Numéro CAS 
1301706-41-1
Formule moléculaire
C36H52N2O5
Poids moléculaire 
592.82
Point de fusion 
145-150 °C
Rotation optique 
[a] D 20 = -7 ± 2º (C = 1 dans DMF)
Informations générales
Numéro CAS 
1301706-41-1
Formule moléculaire
C36H52N2O5
Poids moléculaire 
592.82
Point de fusion 
145-150 °C
Rotation optique 
[a] D 20 = -7 ± 2º (C = 1 dans DMF)
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-Fmoc-Nd-palmitoyl-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 creating modified peptides that can enhance stability and bioactivity.
  • Drug Delivery Systems: Its unique structure allows for the development of liposomal formulations, improving the delivery of therapeutic agents to target cells, which is crucial in cancer treatment.
  • Bioconjugation: The compound can be used to attach bioactive molecules to surfaces or other biomolecules, facilitating the creation of targeted therapies and diagnostic tools.
  • Cosmetic Applications: Due to its biocompatibility, it is explored in skincare formulations aimed at improving skin penetration of active ingredients, enhancing their efficacy.
  • Research in Membrane Biology: It is utilized in studies involving membrane interactions, helping researchers understand how peptides interact with lipid bilayers, which is essential for drug design.

Citations