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Catalog Number:
30316
CAS Number:
878797-01-4
Fmoc-Phe-Ser[Psi (Moi, Moi) Pro]-OH
Purity:
90 - 100 % (dosage par titrage)
Synonym(s):
Fmoc-Phe-Ser[Ψ(Me,Me)Pro]-OH, Acide (S)-3-[N-(9-fluorénylméthyloxycarbonyl)-L-phénylalaninyl]-2,2-diméthyloxazolidine-4-carboxylique
Antibiotic
Documents
$66.80 /1G
Taille
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Informations sur le produit

Fmoc-Phe-Ser[Psi(Me,Me)Pro]-OH is a specialized amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is widely recognized for its effectiveness in solid-phase peptide synthesis. The unique structure of Fmoc-Phe-Ser[Psi(Me,Me)Pro]-OH allows for enhanced stability and reactivity, making it an ideal choice for researchers focusing on the design of bioactive peptides and therapeutic agents. Its application extends to the development of peptide-based drugs, where precise control over the peptide sequence and structure is essential for achieving desired biological activities.

In addition to its utility in peptide synthesis, Fmoc-Phe-Ser[Psi(Me,Me)Pro]-OH is also valuable in the study of protein interactions and the development of novel biomaterials. Researchers can leverage its properties to explore new avenues in drug delivery systems and targeted therapies. The compound's ability to facilitate the incorporation of non-standard amino acids into peptides further enhances its appeal, providing a versatile tool for those in the pharmaceutical and biotechnology sectors.

Numéro CAS 
878797-01-4
Formule moléculaire
C30H30N2O6
Poids moléculaire 
514.58
Informations générales
Numéro CAS 
878797-01-4
Formule moléculaire
C30H30N2O6
Poids moléculaire 
514.58
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-Phe-Ser[Psi(Me,Me)Pro]-OH 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 high specificity and efficiency.
  • Drug Development: It plays a significant role in the development of peptide-based therapeutics, particularly in designing drugs that target specific biological pathways.
  • Bioconjugation: The compound is used in bioconjugation processes to attach peptides to various biomolecules, enhancing the functionality and targeting of therapeutic agents.
  • Research in Protein Engineering: It aids in the modification of proteins, providing insights into protein structure and function, which is crucial for understanding diseases and developing treatments.
  • Diagnostic Applications: This chemical is also explored in the creation of diagnostic tools, particularly in assays that require high specificity to detect biomarkers in clinical settings.

Citations