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Catalog Number:
11960
CAS Number:
353236-19-8
N α - Fmoc- N γ -xanthyl-D-asparagine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-Nγ-xanthyl-D-asparagine
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$72.31 /1G
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Informations sur le produit

Na-Fmoc-Ng-xanthyl-D-asparagine is a specialized amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound is particularly valued in the field of medicinal chemistry for its ability to enhance the stability and solubility of peptides, making it an essential building block in the design of therapeutic agents. Its unique structure, featuring the Fmoc (9-fluorenylmethoxycarbonyl) protecting group and the xanthyl moiety, allows for selective reactions that are vital in the synthesis of complex peptides.

Researchers and industry professionals utilize Na-Fmoc-Ng-xanthyl-D-asparagine in various applications, including the development of peptide-based drugs and the study of protein interactions. Its ability to improve the pharmacokinetic properties of peptides makes it a preferred choice for those looking to optimize drug efficacy. Additionally, its compatibility with solid-phase peptide synthesis techniques ensures that it can be easily integrated into existing workflows, providing a significant advantage over similar compounds.

Numéro CAS 
353236-19-8
Formule moléculaire
C32H26N2O6
Poids moléculaire 
534.54
Point de fusion 
211-217 °C
Rotation optique 
[α] D 20 = +4 ± 2º (C=1 dans DMF)
Informations générales
Numéro CAS 
353236-19-8
Formule moléculaire
C32H26N2O6
Poids moléculaire 
534.54
Point de fusion 
211-217 °C
Rotation optique 
[α] D 20 = +4 ± 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-Ng-xanthyl-D-asparagine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing researchers to selectively modify amino acids without affecting others. This is crucial for creating complex peptides used in drug development.
  • Bioconjugation: It plays a significant role in bioconjugation processes, where it can be attached to biomolecules for targeted drug delivery systems. This enhances the efficacy of therapeutic agents in treating diseases.
  • Fluorescent Probes: The xanthyl group provides fluorescent properties, making it useful in developing fluorescent probes for imaging biological processes in live cells, aiding in research on cellular mechanisms.
  • Drug Discovery: In medicinal chemistry, this compound is valuable for screening libraries of compounds to identify potential drug candidates, especially those targeting specific receptors or enzymes.
  • Research in Neuroscience: Its unique structure is beneficial in studying neurotransmitter interactions, helping researchers understand neurological pathways and develop treatments for neurodegenerative diseases.

Citations