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Catalog Number:
30312
CAS Number:
339531-50-9
Fmoc-Leu-Ser[Psi (Me,Me) Pro]-OH
Purity:
≥ 98,5 % (HPLC)
Synonym(s):
Fmoc-Leu-Ser[Ψ(Me,Me)Pro]-OH, (Ácido S -3-[ N -(9-fluorenilmetiloxicarbonil)-L-leucinil]-2,2-dimetiloxazolidina-4-carboxílico
Antibiotic
Documents
$85.00 /1G
Tamaño
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Información del producto

Fmoc-Leu-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-Leu-Ser[Psi(Me,Me)Pro]-OH allows for enhanced stability and selectivity during the synthesis process, making it an excellent choice for researchers focused on developing complex peptides and biologically active compounds. Its application extends to the pharmaceutical industry, particularly in the design of peptide-based therapeutics, where precision and efficiency are paramount.

This compound is particularly advantageous due to its ability to facilitate the incorporation of non-standard amino acids into peptide chains, thus expanding the potential for novel therapeutic agents. Researchers can leverage its properties to explore new drug candidates with improved efficacy and reduced side effects. Fmoc-Leu-Ser[Psi(Me,Me)Pro]-OH is an essential tool for those aiming to innovate in peptide chemistry and biopharmaceuticals, providing a reliable and effective means to achieve their research goals.

Número CAS
339531-50-9
Fórmula molecular
C27H32N2O6
Peso molecular
480.56
Número MDL
MFCD03490501
Condiciones
Conservar a ≤ -4 °C
Información general
Número CAS
339531-50-9
Fórmula molecular
C27H32N2O6
Peso molecular
480.56
Número MDL
MFCD03490501
Condiciones
Conservar a ≤ -4 °C
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

Fmoc-Leu-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 therapeutic agents. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for easy removal during the synthesis process, enhancing efficiency.
  • Drug Development: Researchers leverage its unique structure to create novel drug candidates, especially in the field of oncology and infectious diseases, where peptide-based therapies are gaining traction.
  • Bioconjugation: The compound is valuable for bioconjugation applications, enabling the attachment of peptides to other biomolecules, which is crucial for creating targeted drug delivery systems.
  • Protein Engineering: It plays a significant role in protein engineering, allowing scientists to modify protein structures for improved stability and functionality, which is essential in biopharmaceuticals.
  • Research in Neuroscience: The compound is also explored in neuroscience research for its potential in developing neuroprotective agents, contributing to advancements in treatments for neurodegenerative diseases.

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