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Catalog Number:
03694
CAS Number:
131287-39-3
N α -Fmoc- N γ -(2-acétamido-2-désoxy-3,4,6-tri- O -acétyl-β-glucopyranosyl)-L-asparagine
Purity:
≥ 97 % (HPLC)
Synonym(s):
Fmoc-L-Asn(GlcNAc(Ac)3-β)-OH
Documents
$198.30 /25 mg
Taille
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Informations sur le produit

Na-Fmoc-Ng-(2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-b-glucopyranosyl)-L-asparagine is a versatile compound widely utilized in peptide synthesis and bioconjugation applications. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which is essential for the selective protection of amines during peptide synthesis. Its structure incorporates a glucosamine derivative, enhancing its solubility and stability, making it an ideal choice for researchers working in the fields of medicinal chemistry and biochemistry.

The compound's ability to facilitate the synthesis of glycopeptides allows for the exploration of glycosylation effects on biological activity, which is crucial in drug development and vaccine research. Additionally, its application in the development of targeted therapeutics highlights its importance in advancing personalized medicine. Researchers can leverage this compound to create complex biomolecules that mimic natural processes, thereby enhancing the efficacy of therapeutic agents. With its unique properties, Na-Fmoc-Ng-(2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-b-glucopyranosyl)-L-asparagine stands out as a valuable tool for innovative research and development in the pharmaceutical industry.

Numéro CAS 
131287-39-3
Formule moléculaire
C33H37N3O13
Poids moléculaire 
683.67
Rotation optique 
[a] D 25 = 20 ± 2,5 º (C = 1 % en TFE)
Informations générales
Numéro CAS 
131287-39-3
Formule moléculaire
C33H37N3O13
Poids moléculaire 
683.67
Rotation optique 
[a] D 25 = 20 ± 2,5 º (C = 1 % en TFE)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Na-Fmoc-Ng-(2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-b-glucopyranosyl)-L-asparagine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in peptide synthesis, allowing for the selective modification of amino acids, which is crucial for creating complex peptides used in pharmaceuticals.
  • Glycopeptide Development: It plays a significant role in the development of glycopeptides, which are important in drug delivery systems and can enhance the efficacy of therapeutic agents.
  • Bioconjugation: The compound is used in bioconjugation techniques, enabling the attachment of biomolecules to surfaces or other molecules, which is essential in diagnostics and targeted therapies.
  • Research in Glycobiology: It aids researchers in studying carbohydrate-protein interactions, providing insights into biological processes and disease mechanisms, particularly in cancer and infectious diseases.
  • Drug Formulation: This chemical is utilized in the formulation of new drug candidates, improving their stability and bioavailability, which is vital for effective treatment outcomes.

Citations