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Catalog Number:
48154
CAS Number:
1260093-07-9
Fmoc-Asn(Trt)-Gly-OH
Purity:
≥ 98 % (HPLC)
Synonym(s):
Na-Fmoc-Ng-Trityl-L-aspariginylglycine
Documents
$55.00 /100 mg
Taille
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Informations sur le produit

Fmoc-Asn(Trt)-Gly-OH is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during solid-phase peptide synthesis. The trityl (Trt) group enhances stability and solubility, making it an excellent choice for researchers aiming to synthesize complex peptides with high purity. Its unique structure allows for efficient coupling reactions, facilitating the assembly of peptides with specific sequences and functionalities.

In the pharmaceutical industry, Fmoc-Asn(Trt)-Gly-OH is particularly valuable for the development of therapeutic peptides and proteins. Its ability to provide a stable and easily removable protecting group streamlines the synthesis process, reducing the risk of side reactions and improving overall yield. Researchers in biochemistry and molecular biology can leverage this compound to create custom peptides for drug discovery, vaccine development, and various applications in biotechnology. With its reliable performance and compatibility with standard peptide synthesis protocols, Fmoc-Asn(Trt)-Gly-OH is an indispensable tool for professionals in the field.

Numéro CAS 
1260093-07-9
Formule moléculaire
C40H35N3O6
Poids moléculaire 
653.72
Informations générales
Numéro CAS 
1260093-07-9
Formule moléculaire
C40H35N3O6
Poids moléculaire 
653.72
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

Fmoc-Asn(Trt)-Gly-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound is a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS), allowing for the creation of complex peptide structures efficiently.
  • Drug Development: It plays a crucial role in the development of peptide-based therapeutics, offering a way to modify peptide sequences for enhanced stability and bioactivity, which is essential in pharmaceutical research.
  • Bioconjugation: Used in bioconjugation techniques, it enables the attachment of peptides to various biomolecules, facilitating the creation of targeted drug delivery systems and diagnostic agents.
  • Protein Engineering: This compound aids in the design of modified proteins with specific functionalities, helping researchers to tailor proteins for industrial applications, such as enzyme production or biosensors.
  • Research in Neuroscience: It is utilized in studies related to neuropeptides, contributing to the understanding of neurological processes and potential treatments for neurodegenerative diseases.

Citations