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Catalog Number:
30308
CAS Number:
1095952-22-9
Fmoc-Gly-Ser[Psi (Me,Me) Pro]-OH
Purity:
≥ 97 % (HPLC)
Synonym(s):
Fmoc-Gly-Ser[Ψ(Me,Me)Pro]-OH, Acide (S)-3-[N-(9-fluorénylméthyloxycarbonyl)-glycinyl]-2,2-diméthyloxazolidine-4-carboxylique
Antibiotic
Documents
$77.82 /1G
Taille
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Informations sur le produit

Fmoc-Gly-Ser[Psi(Me,Me)Pro]-OH is a versatile building block in peptide synthesis, particularly valuable for researchers focused on developing complex peptides and proteins. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is widely recognized for its stability and ease of removal under mild conditions, making it an ideal choice for solid-phase peptide synthesis. The incorporation of the Psi(Me,Me)Pro residue enhances the structural diversity of peptides, allowing for the exploration of unique conformations and biological activities.

In practical applications, Fmoc-Gly-Ser[Psi(Me,Me)Pro]-OH can be utilized in the design of peptide-based therapeutics, including those targeting specific biological pathways or diseases. Its unique properties facilitate the synthesis of peptides with improved stability and bioactivity, which can be crucial in drug development and research. This compound is particularly beneficial for professionals in pharmaceutical research, biochemistry, and molecular biology, providing them with a reliable tool for advancing their projects.

Numéro CAS 
1095952-22-9
Formule moléculaire
C23H24N2O6
Poids moléculaire 
424.45
Rotation optique 
[a]25D = -34 ± 2,5 º (C=1 dans MeOH)
Informations générales
Numéro CAS 
1095952-22-9
Formule moléculaire
C23H24N2O6
Poids moléculaire 
424.45
Rotation optique 
[a]25D = -34 ± 2,5 º (C=1 dans MeOH)
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-Gly-Ser[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, allowing researchers to create specific sequences for various applications in drug development and biotechnology.
  • Drug Design: Its unique structure aids in the design of peptide-based drugs, particularly those 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 other molecules, such as antibodies, which is essential for developing targeted therapies.
  • Research in Protein Engineering: It plays a role in protein engineering studies, helping scientists modify proteins for improved stability and functionality, which is vital in various industrial applications.
  • Analytical Chemistry: Fmoc-Gly-Ser[Psi(Me,Me)Pro]-OH is utilized in analytical methods to study peptide interactions, providing insights into molecular behavior and aiding in the development of new analytical techniques.

Citations