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Catalog Number:
03746
CAS Number:
191348-16-0
Fmoc -O -benzylphospho-L-tyrosine
Purity:
≥ 97 % (HPLC)
Synonym(s):
Fmoc-L-Tyr(HPO3Bzl)-OH
Documents
$108.26 /250 mg
Taille
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Informations sur le produit

Fmoc-O-benzylphospho-L-tyrosine is a versatile phosphotyrosine derivative that plays a crucial role in peptide synthesis and bioconjugation applications. This compound is particularly valued in the fields of medicinal chemistry and biochemistry for its ability to mimic phosphorylated tyrosine residues, which are essential in various cellular signaling pathways. Researchers utilize Fmoc-O-benzylphospho-L-tyrosine to study protein interactions and enzyme activities, making it an indispensable tool for drug discovery and development. Its unique Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for straightforward incorporation into peptides, facilitating the synthesis of complex biomolecules.

Moreover, this compound's stability and solubility in organic solvents enhance its usability in various experimental conditions, providing researchers with reliable results. Fmoc-O-benzylphospho-L-tyrosine is also advantageous for developing targeted therapies, as it can be used to create phosphopeptide libraries that aid in the identification of novel therapeutic targets. Its application in the synthesis of phosphopeptides not only streamlines research but also opens avenues for innovative treatments in cancer and other diseases.

Numéro CAS 
191348-16-0
Formule moléculaire
C 31 H 288 P
Poids moléculaire 
573.5
Point de fusion 
131 - 165 °C
Rotation optique 
[a] D 20 = -15 ± 2 º (C = 2 dans DMF)
Informations générales
Numéro CAS 
191348-16-0
Formule moléculaire
C 31 H 288 P
Poids moléculaire 
573.5
Point de fusion 
131 - 165 °C
Rotation optique 
[a] D 20 = -15 ± 2 º (C = 2 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-O-benzylphospho-L-tyrosine is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of phosphopeptides, which are vital for studying protein interactions and signaling pathways.
  • Drug Development: Its role in drug design allows researchers to create targeted therapies that mimic natural phosphoproteins, enhancing the specificity and efficacy of treatments.
  • Bioconjugation: The compound is used in bioconjugation processes to attach biomolecules to surfaces or other molecules, facilitating the development of biosensors and diagnostic tools.
  • Research in Cancer Biology: By studying the interactions of phosphopeptides containing this compound, scientists can gain insights into cancer cell signaling, potentially leading to new therapeutic strategies.
  • Analytical Chemistry: It is employed in various analytical techniques, such as mass spectrometry, to help identify and quantify phosphoproteins, contributing to a better understanding of cellular processes.

Citations