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Catalog Number:
04990
CAS Number:
204260-38-8
Fmoc-4-méthyl-D-phénylalanine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-D-Phe(4-Me)-OH, Fmoc- p -Me-D-Phe-OH
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$43.87 /1G
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Informations sur le produit

Fmoc-4-methyl-D-phenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during solid-phase peptide synthesis. Its unique structure, characterized by the presence of a 4-methylphenyl side chain, enhances the hydrophobic interactions in peptides, making it particularly valuable in the design of bioactive compounds and pharmaceuticals. Researchers appreciate its stability and compatibility with various coupling reagents, which facilitates the efficient assembly of complex peptide sequences.

In addition to its role in peptide synthesis, Fmoc-4-methyl-D-phenylalanine has shown potential in the development of novel therapeutics, particularly in the fields of cancer and neurodegenerative diseases. Its ability to influence peptide conformation and bioactivity makes it a critical component in the creation of targeted drug delivery systems. By incorporating this compound into their research, scientists can explore new avenues for drug design and enhance the efficacy of therapeutic agents.

Numéro CAS 
204260-38-8
Formule moléculaire
C 25 H 234
Poids moléculaire 
401.46
Point de fusion 
167-172 °C
Rotation optique 
[a] D 20 = +27 ± 2º (C = 1 dans DMF)
Informations générales
Numéro CAS 
204260-38-8
Formule moléculaire
C 25 H 234
Poids moléculaire 
401.46
Point de fusion 
167-172 °C
Rotation optique 
[a] D 20 = +27 ± 2º (C = 1 dans DMF)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Fmoc-4-methyl-D-phenylalanine is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS). Its protective Fmoc group allows for selective deprotection, facilitating the assembly of complex peptide sequences.
  • Drug Development: Researchers leverage its unique properties to create peptide-based drugs. Its ability to mimic natural amino acids makes it valuable in designing therapeutics that target specific biological pathways.
  • Bioconjugation: The compound is used in bioconjugation techniques, where it helps attach peptides to various biomolecules, enhancing the specificity and efficacy of drug delivery systems.
  • Research in Neuroscience: Due to its structural similarity to certain neurotransmitters, it is used in studies exploring receptor binding and the development of neuroactive compounds, aiding in the understanding of neurological disorders.
  • Custom Peptide Libraries: Fmoc-4-methyl-D-phenylalanine is instrumental in creating custom peptide libraries for high-throughput screening, allowing researchers to identify potential drug candidates efficiently.

Citations