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Catalog Number:
02466
CAS Number:
147688-40-2
Fmoc- O -2-bromo-ZL-tyrosine
Purity:
≥ 97 % (HPLC)
Synonym(s):
Fmoc-L-Tyr(2-Br-Z)-OH
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$18.53 /1G
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Informations sur le produit

Fmoc-O-2-bromo-Z-L-tyrosine is a specialized amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its brominated phenyl group enhances the compound's reactivity, making it a valuable building block in the creation of complex peptides and proteins. Researchers and industry professionals appreciate its role in solid-phase peptide synthesis (SPPS), where it facilitates the assembly of peptides with high purity and yield.

Moreover, Fmoc-O-2-bromo-Z-L-tyrosine is particularly advantageous for the development of bioactive compounds, including those used in pharmaceuticals and biotechnology. Its unique structure allows for the incorporation of specific functionalities, which can lead to the discovery of novel therapeutic agents. With its proven efficacy in peptide synthesis and potential applications in drug design, this compound is an essential tool for researchers aiming to innovate in the fields of medicinal chemistry and biochemistry.

Numéro CAS 
147688-40-2
Formule moléculaire
C 32 H 26 NO 7 Br
Poids moléculaire 
616.5
Rotation optique 
[a] 20 D = -11 ± 2 º (C=1 dans DMF)
Informations générales
Numéro CAS 
147688-40-2
Formule moléculaire
C 32 H 26 NO 7 Br
Poids moléculaire 
616.5
Rotation optique 
[a] 20 D = -11 ± 2 º (C=1 dans 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-O-2-bromo-Z-L-tyrosine 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), allowing for the creation of complex peptide sequences.
  • Drug Development: Its unique brominated structure can enhance the biological activity of peptide-based drugs, making it valuable in the pharmaceutical industry for developing new therapeutics.
  • Bioconjugation: The compound can be used in bioconjugation processes to attach peptides to various biomolecules, facilitating the creation of targeted drug delivery systems.
  • Research in Cancer Therapy: Due to its potential to modify peptide properties, it is being explored in cancer research for designing targeted therapies that can selectively attack cancer cells.
  • Protein Engineering: The compound aids in the modification of proteins to study their structure and function, providing insights that can lead to advancements in biotechnology and molecular biology.

Citations