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Catalog Number:
15038
CAS Number:
957311-37-4
Acide Fmoc-L-glutamique α-7-amido-4-méthylcoumarine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Acide Fmoc-L-glutamique α-7-amido-4-méthylcoumarine
Documents
$106.96 /250 mg
Taille
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Informations sur le produit

Fmoc-L-glutamic acid a-7-amido-4-methylcoumarin is a versatile compound widely utilized in peptide synthesis and bioconjugation applications. This derivative of glutamic acid features a protective Fmoc (fluorenylmethyloxycarbonyl) group, which facilitates the selective coupling of amino acids in solid-phase peptide synthesis. Its unique structure, incorporating a 4-methylcoumarin moiety, enhances its utility in fluorescence-based assays, making it an excellent choice for researchers focusing on bioimaging and drug delivery systems.

The compound's ability to serve as a fluorescent probe allows for real-time monitoring of peptide interactions and cellular processes, providing valuable insights in biochemical research. Additionally, its stability and compatibility with various reaction conditions make it a preferred choice for synthetic chemists looking to develop novel peptides with specific functionalities. With its dual role as a building block and a fluorescent marker, Fmoc-L-glutamic acid a-7-amido-4-methylcoumarin stands out in the field of chemical biology and medicinal chemistry.

Numéro CAS 
957311-37-4
Formule moléculaire
C30H26N2O7
Poids moléculaire 
526.54
Point de fusion 
214-223 °C
Rotation optique 
[a] D 20 = -50 ± 2º (C = 1 dans DMF)
Informations générales
Numéro CAS 
957311-37-4
Formule moléculaire
C30H26N2O7
Poids moléculaire 
526.54
Point de fusion 
214-223 °C
Rotation optique 
[a] D 20 = -50 ± 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-L-glutamic acid a-7-amido-4-methylcoumarin 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, allowing for the creation of complex peptide sequences with high purity.
  • Fluorescent Probes: Its unique structure enables its use as a fluorescent probe in biochemical assays, helping researchers visualize and track biological processes in real-time.
  • Drug Development: The compound is explored in medicinal chemistry for the development of new drugs, particularly those targeting specific proteins, due to its ability to modify biological activity.
  • Bioconjugation: It is applied in bioconjugation techniques, linking biomolecules to enhance their stability and efficacy, which is crucial in therapeutic applications.
  • Research in Neuroscience: The compound is utilized in studies related to neurotransmitter signaling, aiding in the understanding of neurological pathways and potential treatments for neurodegenerative diseases.

Citations