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Catalog Number:
30313
CAS Number:
955048-89-2
Fmoc-Leu-Thr[Psi (Me,Me) Pro]-OH
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-Leu-Thr[Y(Me,Me)Pro]-OH, Acide (4S,5R)-3-[N-(9-fluorénylméthyloxycarbonyl)-L-leucinyl]-2,2,5-triméthyloxazolidine-4-carboxylique
Antibiotic
Documents
$85.00 /1G
Taille
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Informations sur le produit

Fmoc-Leu-Thr[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-Leu-Thr[Psi(Me,Me)Pro]-OH allows for enhanced stability and selectivity during the synthesis process, making it an ideal choice for researchers focused on developing complex peptides and biologically active compounds.

In addition to its utility in peptide synthesis, this compound is particularly valuable in the pharmaceutical industry for the design of peptide-based therapeutics. Its specific configuration promotes favorable interactions in biological systems, potentially leading to improved efficacy and reduced side effects in drug formulations. Researchers can leverage the unique properties of Fmoc-Leu-Thr[Psi(Me,Me)Pro]-OH to explore novel therapeutic avenues, particularly in the fields of oncology and immunology, where peptide-based strategies are gaining traction.

Numéro CAS 
955048-89-2
Formule moléculaire
C28H34N2O6
Poids moléculaire 
494.59
Informations générales
Numéro CAS 
955048-89-2
Formule moléculaire
C28H34N2O6
Poids moléculaire 
494.59
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-Leu-Thr[Psi(Me,Me)Pro]-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a crucial building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing researchers to create complex peptide sequences efficiently.
  • Drug Development: It plays a significant role in the pharmaceutical industry for developing peptide-based drugs, offering potential therapeutic benefits in treating various diseases.
  • Bioconjugation: The chemical is used in bioconjugation processes, enabling the attachment of peptides to other biomolecules, which is essential for creating targeted drug delivery systems.
  • Research in Protein Engineering: It aids in the design and modification of proteins, helping scientists explore new functionalities and improve the stability of therapeutic proteins.
  • Analytical Chemistry: This compound is utilized in analytical methods to study peptide interactions and stability, providing valuable insights for researchers in biochemistry and molecular biology.

Citations