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Catalog Number:
48168
CAS Number:
288149-55-3
Fmoc-Glu-NH2
Purity:
≥ 95 % (HPLC)
Synonym(s):
Na-Fmoc-L-glutamylamide
Documents
$35.00 /100 mg
Taille
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Informations sur le produit

Fmoc-Glu-NH2 is a versatile amino acid derivative widely utilized in peptide synthesis and research applications. This compound, known for its protective Fmoc (9-fluorenylmethyloxycarbonyl) group, facilitates the efficient assembly of peptides by providing a stable and easily removable protecting group for the amino functionality. Its unique structure allows for the selective introduction of the glutamic acid residue into peptides, making it invaluable in the development of bioactive compounds, pharmaceuticals, and research reagents.

Researchers and industry professionals appreciate Fmoc-Glu-NH2 for its role in enhancing the solubility and stability of peptides, which is crucial for various applications, including drug development and therapeutic protein engineering. The compound's ability to streamline the synthesis process while maintaining high purity levels makes it a preferred choice in laboratories focused on peptide chemistry. With its proven track record in facilitating complex peptide synthesis, Fmoc-Glu-NH2 stands out as an essential tool for advancing research in biochemistry and molecular biology.

Numéro CAS 
288149-55-3
Formule moléculaire
C20H20N2O5
Poids moléculaire 
368.38
Informations générales
Numéro CAS 
288149-55-3
Formule moléculaire
C20H20N2O5
Poids moléculaire 
368.38
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-Glu-NH2 is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures for various applications in drug development.
  • Drug Discovery: Its role in modifying amino acids makes it essential in the design of novel therapeutics, particularly in targeting specific biological pathways.
  • Bioconjugation: Fmoc-Glu-NH2 is used in bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is crucial in developing biosensors and diagnostic tools.
  • Research in Neuroscience: This compound is valuable in studying neurotransmitter systems, as it can be incorporated into peptides that mimic or inhibit natural signaling pathways.
  • Protein Engineering: It aids in the modification of proteins, enhancing their stability and functionality, which is vital for applications in biotechnology and pharmaceuticals.

Citations