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Catalog Number:
30320
CAS Number:
878797-09-2
Fmoc-Tyr(tBu)-Ser[Psi (Me,Me) Pro]-OH
Purity:
≥ 98,5 % (HPLC)
Synonym(s):
Fmoc-Tyr(tBu)-Ser[Y(Me,Me)Pro]-OH, Acide (S)-3-[Na-(9-fluorénylméthyloxycarbonyl)-O-tert-butyl-L-tyrosinyl]-2,2-diméthyloxazolidine-4-carboxylique
Antibiotic
Documents
$85.00 /1G
Taille
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Informations sur le produit

Fmoc-Tyr(tBu)-Ser[Psi(Me,Me)Pro]-OH is a specialized 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 complex peptides. Its unique structure, incorporating a t-butyl (tBu) group and a Psi(Me,Me)Pro modification, enhances stability and solubility, making it particularly valuable in the formulation of therapeutic peptides. Researchers and industry professionals can leverage this compound for the development of peptide-based drugs, particularly in oncology and immunology, where precise modifications can significantly influence biological activity and efficacy.

The compound's ability to facilitate the synthesis of peptides with enhanced pharmacological properties positions it as a critical tool in medicinal chemistry. Its unique features, such as improved stability and solubility, provide advantages over traditional amino acids, allowing for more efficient synthesis and better yields. Fmoc-Tyr(tBu)-Ser[Psi(Me,Me)Pro]-OH is an excellent choice for those looking to innovate in peptide design and development, ensuring high-quality results in research and application.

Numéro CAS 
878797-09-2
Formule moléculaire
C34H38N2O7
Poids moléculaire 
586.68
Informations générales
Numéro CAS 
878797-09-2
Formule moléculaire
C34H38N2O7
Poids moléculaire 
586.68
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-Tyr(tBu)-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, particularly in solid-phase peptide synthesis (SPPS), allowing for the creation of complex peptide sequences with high purity and yield.
  • Drug Development: Researchers use this compound to develop peptide-based drugs, especially in targeting specific diseases, due to its ability to enhance the stability and bioavailability of therapeutic peptides.
  • Bioconjugation: It is employed in bioconjugation processes, where it helps in attaching peptides to other molecules, such as antibodies or drugs, facilitating targeted delivery systems in cancer therapy.
  • Protein Engineering: This chemical is useful in the modification of proteins to study structure-function relationships, aiding in the design of proteins with enhanced properties for industrial applications.
  • Research in Neuroscience: The compound is utilized in studies related to neuropeptides, contributing to the understanding of neurological functions and potential treatments for neurodegenerative diseases.

Citations