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Catalog Number:
30314
CAS Number:
957780-54-0
Fmoc-Lys(Boc)-Ser[Psi (Me,Me) Pro]-OH
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-Lys(Boc)-Ser[Ψ(Me,Me)Pro]-OH, Acide (S)-3-[Na-(9-fluorénylméthyloxycarbonyl)-Ne-tert-butyloxycarbonyl-L-lysinyl]-2,2-diméthyloxazolidine-4-carboxylique
Antibiotic
Documents
$83.32 /1G
Taille
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Informations sur le produit

Fmoc-Lys(Boc)-Ser[Psi(Me,Me)Pro]-OH is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a unique structure that incorporates a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino acids during solid-phase peptide synthesis. The Boc (tert-butyloxycarbonyl) group further enhances its stability and compatibility with various coupling reactions, making it an ideal choice for researchers focused on synthesizing complex peptides and proteins.

In addition to its role in peptide synthesis, this compound is particularly valuable in the development of peptide-based therapeutics and biomaterials. Its unique properties allow for the incorporation of specific functionalities that can enhance bioactivity and stability in pharmaceutical applications. Researchers in the fields of medicinal chemistry and biochemistry will find Fmoc-Lys(Boc)-Ser[Psi(Me,Me)Pro]-OH to be an essential tool in their quest for innovative solutions in drug design and delivery.

Numéro CAS 
957780-54-0
Formule moléculaire
C32H41N3O8
Poids moléculaire 
595.69
Rotation optique 
[a]25D = -32 ± 3,5 º (C=1 dans CH2Cl2 )
Informations générales
Numéro CAS 
957780-54-0
Formule moléculaire
C32H41N3O8
Poids moléculaire 
595.69
Rotation optique 
[a]25D = -32 ± 3,5 º (C=1 dans CH2Cl2 )
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Fmoc-Lys(Boc)-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 and functional peptide sequences.
  • Drug Development: It plays a crucial role in developing peptide-based pharmaceuticals, especially in targeting specific biological pathways, enhancing therapeutic efficacy, and reducing side effects.
  • Bioconjugation: The compound is used in bioconjugation processes, facilitating the attachment of peptides to various biomolecules, which is essential in creating targeted drug delivery systems.
  • Research in Protein Engineering: It aids researchers in modifying proteins to study structure-function relationships, enabling advancements in biotechnology and synthetic biology.
  • Diagnostics: This chemical is valuable in the development of diagnostic tools, particularly in creating peptide-based assays that improve the sensitivity and specificity of disease detection.

Citations