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Catalog Number:
02579
CAS Number:
132684-59-4
Fmoc-L-homophénylalanine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-HomoPhe-OH, Acide ( S )-2-(Fmoc-amino)-4-phényl-butyrique, Fmoc-HomoPhe-OH
Documents
$18.53 /1G
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Informations sur le produit

Fmoc-L-homophenylalanine is a valuable amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which enhances its stability and solubility, making it an excellent choice for solid-phase peptide synthesis. Researchers appreciate its ability to facilitate the introduction of phenylalanine-like residues into peptides, thereby improving the pharmacological properties of the resulting compounds.

In addition to its role in peptide synthesis, Fmoc-L-homophenylalanine is also employed in the development of novel therapeutics, particularly in the fields of oncology and neurology. Its unique structure allows for the exploration of new peptide-based drugs that can target specific biological pathways. The compound's compatibility with various coupling reagents and its ease of deprotection further enhance its appeal to researchers seeking efficient and effective synthesis methods.

Numéro CAS 
132684-59-4
Formule moléculaire
C 25 H 234
Poids moléculaire 
401.45
Point de fusion 
142 - 159 °C
Rotation optique 
[a] D 20 = -9 ± 2 ° (C = 1, DMF)
Informations générales
Numéro CAS 
132684-59-4
Formule moléculaire
C 25 H 234
Poids moléculaire 
401.45
Point de fusion 
142 - 159 °C
Rotation optique 
[a] D 20 = -9 ± 2 ° (C = 1, DMF)
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-L-homophenylalanine is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in solid-phase peptide synthesis, allowing researchers to create complex peptides with high purity and yield.
  • Drug Development: Its unique structure makes it valuable in the design of peptide-based drugs, particularly in targeting specific biological pathways.
  • Bioconjugation: Fmoc-L-homophenylalanine can be used in bioconjugation processes, facilitating the attachment of peptides to various biomolecules for therapeutic applications.
  • Research in Neuroscience: This compound is employed in studies related to neurotransmitter function and receptor interactions, aiding in the understanding of neurological disorders.
  • Custom Peptide Libraries: It is instrumental in creating diverse peptide libraries for screening potential drug candidates, enhancing the efficiency of drug discovery processes.

Citations