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Catalog Number:
05749
CAS Number:
201046-57-3
Chlorhydrate de N α -Fmoc- N δ -L-ornithine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-L-Orn-OH·HCl
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$65.40 /1G
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Informations sur le produit

Na-Fmoc-Nd-L-ornithine hydrochloride is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protective group, which is essential for the selective protection of amine functionalities during the synthesis of complex peptides. Its unique structure allows for efficient coupling reactions, making it an ideal choice for researchers looking to streamline their synthesis processes. The hydrochloride form enhances its solubility in aqueous solutions, facilitating its use in various biological applications, including the development of peptide-based therapeutics and research into protein interactions.

In addition to its role in peptide synthesis, Na-Fmoc-Nd-L-ornithine hydrochloride is also valuable in the study of neuropeptides and other biologically active compounds. Its ability to provide stability and enhance the bioavailability of peptides makes it a preferred choice among researchers in medicinal chemistry and biochemistry. With its robust performance in synthetic applications and potential for innovative therapeutic development, this compound stands out as a critical tool for professionals in the pharmaceutical and biotechnology industries.

Numéro CAS 
201046-57-3
Formule moléculaire
C20H22N2O4 · HCl
Poids moléculaire 
390.91
Point de fusion 
130 - 170 °C
Rotation optique 
[a] 20 D
Informations générales
Numéro CAS 
201046-57-3
Formule moléculaire
C20H22N2O4 · HCl
Poids moléculaire 
390.91
Point de fusion 
130 - 170 °C
Rotation optique 
[a] 20 D
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-L-ornithine hydrochloride 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 Fmoc group allows for selective deprotection during the synthesis process.
  • Drug Development: Researchers leverage its properties to create novel drug candidates, especially in the field of cancer therapy, where specific peptide sequences can inhibit tumor growth.
  • Bioconjugation: It is used in bioconjugation techniques to attach peptides to various biomolecules, enhancing the efficacy of drug delivery systems.
  • Research in Neuroscience: The compound is explored in neuroscience for developing neuropeptides that can modulate neurological functions, offering potential treatments for neurodegenerative diseases.
  • Analytical Chemistry: It plays a role in analytical methods, such as mass spectrometry, to identify and quantify peptide structures, aiding in the characterization of complex biological samples.

Citations