Découvrez le nouveau Chem-Impex : là où l'innovation commence par une liaison.

Catalog Number:
04828
CAS Number:
212688-51-2
Fmoc- O -trityl-D-sérine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-D-Ser(Trt)-OH
Documents
$29.34 /1G
Taille
Request Bulk Quote
Informations sur le produit

Fmoc-O-trityl-D-serine is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a protective Fmoc (9-fluorenylmethoxycarbonyl) group, which allows for selective deprotection during the synthesis process, making it an essential building block for creating complex peptides. Its trityl (Tr) protection enhances stability and solubility, facilitating its use in various organic synthesis applications. Researchers and industry professionals appreciate its role in the development of peptide-based therapeutics, where precise amino acid sequences are crucial for biological activity.

In addition to its applications in peptide synthesis, Fmoc-O-trityl-D-serine is also valuable in the study of protein interactions and enzyme activity. Its unique structure allows for modifications that can lead to the development of novel compounds with enhanced biological properties. This compound is particularly beneficial for those working in drug discovery and development, as it provides a reliable method for constructing peptides that can be screened for therapeutic efficacy. With its robust performance and adaptability, Fmoc-O-trityl-D-serine stands out as a key reagent in modern chemical research.

Numéro CAS 
212688-51-2
Formule moléculaire
C 37 H 315
Poids moléculaire 
569.7
Informations générales
Numéro CAS 
212688-51-2
Formule moléculaire
C 37 H 315
Poids moléculaire 
569.7
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

Fmoc-O-trityl-D-serine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions without interfering with other functional groups. Its stability under various conditions makes it a preferred choice for chemists.
  • Drug Development: In pharmaceutical research, it aids in the design of peptide-based drugs. The ability to modify the structure easily allows researchers to optimize drug efficacy and reduce side effects.
  • Bioconjugation: It is used in the conjugation of peptides to other biomolecules, enhancing the delivery and targeting of therapeutic agents in treatments, particularly in cancer therapy.
  • Protein Engineering: The compound plays a role in the modification of proteins, enabling the introduction of specific functionalities that can improve stability and activity in various applications.
  • Research in Neuroscience: Fmoc-O-trityl-D-serine is valuable in studying neuropeptides, contributing to the understanding of neurological pathways and potential treatments for neurodegenerative diseases.

Citations