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Catalog Number:
30311
CAS Number:
957780-52-8
Fmoc-Ile-Thr[Psi (Me,Me) Pro]-OH
Purity:
95 - 101 % (dosage par titrage)
Synonym(s):
Fmoc-Ile-Thr[Ψ(Me,Me)Pro]-OH, Acide (4S,5R)-3-[N-(9-fluorénylméthyloxycarbonyl)-L-isoleucinyl]-2,2,5-triméthyloxazolidine-4-carboxylique
Antibiotic
Documents
$66.80 /1G
Taille
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Informations sur le produit

Fmoc-Ile-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 unique structure that enhances its stability and bioactivity, making it an invaluable tool for researchers in the fields of medicinal chemistry and biochemistry. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for easy incorporation into peptide chains, facilitating the synthesis of complex peptides with specific functionalities.

This compound is particularly beneficial in the design of peptide-based therapeutics, where precise control over amino acid sequences is essential. Researchers have utilized Fmoc-Ile-Thr[Psi(Me,Me)Pro]-OH in the development of novel peptides that exhibit improved pharmacological properties, such as enhanced receptor binding and increased resistance to enzymatic degradation. Its unique features, including the Psi(Me,Me)Pro modification, provide advantages over traditional amino acids, allowing for greater flexibility and stability in peptide structures. This compound is ideal for professionals seeking to innovate in peptide synthesis and drug formulation.

Numéro CAS 
957780-52-8
Formule moléculaire
C28H34N2O6
Poids moléculaire 
494.59
Rotation optique 
[a]25D = -24,5 ± 2,5 º (C=1 dans MeOH)
Informations générales
Numéro CAS 
957780-52-8
Formule moléculaire
C28H34N2O6
Poids moléculaire 
494.59
Rotation optique 
[a]25D = -24,5 ± 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
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Fmoc-Ile-Thr[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, enabling researchers to create complex sequences for various biological studies.
  • Drug Development: It plays a crucial role in the design of peptide-based drugs, particularly in targeting specific receptors, which can lead to more effective therapies with fewer side effects.
  • Bioconjugation: The compound is used in bioconjugation processes, allowing for the attachment of peptides to other molecules, enhancing the delivery and efficacy of therapeutic agents.
  • Protein Engineering: Researchers utilize it to modify proteins, improving their stability and functionality, which is essential in developing new biotechnological applications.
  • Research in Neuroscience: Its unique structure makes it valuable in studies related to neuropeptides, helping scientists understand brain functions and develop treatments for neurological disorders.

Citations