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Catalog Number:
30304
CAS Number:
955048-92-7
Fmoc-Asp(OtBu)-Ser[Psi (Me,Me) Pro]-OH
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-Asp(OtBu)-Ser[Ψ(Me,Me)Pro]-OH, Acide (S)-3-[Na-(9-fluorénylméthyloxycarbonyl)-L-aspartyl-t-butylester]-2,2-diméthyloxazolidine-4-carboxylique
Antibiotic
Documents
$77.82 /1G
Taille
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Informations sur le produit

Fmoc-Asp(OtBu)-Ser[Psi(Me,Me)Pro]-OH is a sophisticated 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 the synthesis of peptides. Its unique structure, including the tert-butyl ester and the Psi(Me,Me)Pro modification, enhances its stability and solubility, making it an excellent choice for researchers focusing on complex peptide sequences.

In practical applications, Fmoc-Asp(OtBu)-Ser[Psi(Me,Me)Pro]-OH is particularly valuable in the development of therapeutic peptides and proteins, where precise control over amino acid sequences is critical. Its compatibility with various coupling reagents and solid-phase synthesis techniques allows for streamlined workflows in laboratories. Additionally, this compound can be instrumental in the study of protein interactions and the design of novel biomolecules, offering researchers a versatile tool for advancing their projects in medicinal chemistry and biochemistry.

Numéro CAS 
955048-92-7
Formule moléculaire
C29H34N2O8
Poids moléculaire 
538.59
Informations générales
Numéro CAS 
955048-92-7
Formule moléculaire
C29H34N2O8
Poids moléculaire 
538.59
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-Asp(OtBu)-Ser[Psi(Me,Me)Pro] 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 with specific functionalities for drug development.
  • Drug Design: Its unique properties facilitate the design of peptide-based therapeutics, particularly in targeting specific biological pathways, enhancing the efficacy of treatments.
  • Bioconjugation: The compound can be used in bioconjugation processes, linking peptides to other biomolecules, which is crucial for creating targeted drug delivery systems.
  • Research in Neuroscience: It plays a role in studying neuropeptides and their functions, providing insights into neurological disorders and potential therapeutic approaches.
  • Protein Engineering: This chemical is valuable in the field of protein engineering, enabling the modification of proteins to improve their stability and activity for various industrial applications.

Citations