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Catalog Number:
07326
CAS Number:
238084-15-6
Acide Fmoc-L-Aspartique α-7-amido-4-méthylcoumarine
Purity:
≥ 97 % (HPLC)
Synonym(s):
Fmoc-L-Asp-AMC
Documents
$100.05 /100 mg
Taille
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Informations sur le produit

Fmoc-L-Aspartic acid a-7-amido-4-methylcoumarin is a versatile compound widely utilized in peptide synthesis and bioconjugation applications. This derivative of aspartic acid features a protective Fmoc group, which is crucial for the selective deprotection of amino acids during solid-phase peptide synthesis. Its unique structure, incorporating a 4-methylcoumarin moiety, enhances its fluorescence properties, making it an excellent choice for applications in fluorescence-based assays and imaging techniques. Researchers in the fields of biochemistry and molecular biology can leverage this compound for the development of novel peptides and probes, facilitating advancements in drug discovery and diagnostics.

The compound's ability to act as a fluorescent tag allows for real-time monitoring of biological processes, providing valuable insights into cellular mechanisms. Additionally, its stability and compatibility with various reaction conditions make it a preferred choice for synthesizing complex peptide structures. With its dual functionality as both a building block and a fluorescent marker, Fmoc-L-Aspartic acid a-7-amido-4-methylcoumarin stands out as an essential tool for researchers aiming to explore and manipulate biological systems effectively.

Numéro CAS 
238084-15-6
Formule moléculaire
C29H24N2O7
Poids moléculaire 
512.53
Rotation optique 
[α] D 20
Informations générales
Numéro CAS 
238084-15-6
Formule moléculaire
C29H24N2O7
Poids moléculaire 
512.53
Rotation optique 
[α] D 20
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-Aspartic 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 researchers to create complex peptide sequences efficiently.
  • Fluorescent Probes: Its unique structure enables the development of fluorescent probes for biological imaging, helping scientists visualize cellular processes in real-time.
  • Drug Development: The compound is used in medicinal chemistry to design and evaluate new drug candidates, particularly those targeting specific biological pathways.
  • Bioconjugation: It facilitates the attachment of biomolecules to surfaces or other molecules, enhancing the functionality of biosensors and drug delivery systems.
  • Research in Enzyme Activity: This chemical is valuable in studying enzyme kinetics, providing insights into enzyme mechanisms and potential inhibitors.

Citations