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Catalog Number:
30310
CAS Number:
1147996-34-6
Fmoc-Ile-Ser[Psi (Moi,Moi) Pro]-OH
Purity:
99 - 101 % (dosage par titrage)
Synonym(s):
Fmoc-Ile-Ser[Psi(Me,Me)Pro]-OH, Acide (S)-3-[N-(9-fluorénylméthyloxycarbonyl)-L-isoleucinyl]-2,2-diméthyloxazolidine-4-carboxylique
Antibiotic
Documents
$83.32 /1G
Taille
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Informations sur le produit

Fmoc-Ile-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-Ile-Ser[Psi(Me,Me)Pro]-OH allows for enhanced stability and reactivity, making it an ideal choice for researchers focused on developing complex peptides and proteins. Its specific configuration promotes efficient coupling reactions, which are essential in the synthesis of bioactive peptides, including those used in therapeutic applications.

This compound is particularly valuable in the fields of medicinal chemistry and biochemistry, where it can be utilized to create peptides with tailored properties for drug discovery and development. Researchers can leverage its unique characteristics to explore new therapeutic avenues, especially in the design of peptide-based drugs with improved efficacy and reduced side effects. Fmoc-Ile-Ser[Psi(Me,Me)Pro]-OH stands out for its ability to facilitate the synthesis of peptides that mimic natural biological processes, thus holding significant potential for innovative research and applications.

Numéro CAS 
1147996-34-6
Formule moléculaire
C27H32N2O6
Poids moléculaire 
480.56
Rotation optique 
[a]25D = -42 ± 3,5 º (C=1 dans MeOH)
Informations générales
Numéro CAS 
1147996-34-6
Formule moléculaire
C27H32N2O6
Poids moléculaire 
480.56
Rotation optique 
[a]25D = -42 ± 3,5 º (C=1 dans MeOH)
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-Ile-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 the development of pharmaceuticals and biologically active compounds.
  • Drug Development: It plays a significant role in the design of peptide-based drugs, offering improved stability and bioavailability compared to traditional compounds.
  • Bioconjugation: The chemical is used in bioconjugation processes, allowing researchers to attach peptides to other biomolecules, enhancing targeting capabilities in drug delivery systems.
  • Research in Protein Engineering: It aids in the modification of proteins, enabling scientists to explore structure-function relationships and develop novel protein therapeutics.
  • Diagnostic Applications: The compound is utilized in the creation of peptide-based diagnostics, providing sensitive detection methods for various diseases.

Citations