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Catalog Number:
07326
CAS Number:
238084-15-6
Ácido Fmoc-L-aspártico α-7-amido-4-metilcumarina
Purity:
≥ 97 % (HPLC)
Synonym(s):
Fmoc-L-Asp-AMC
Documents
$100.05 /100 mg
Tamaño
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Información del producto

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.

Número CAS
238084-15-6
Fórmula molecular
C29H24N2O7
Peso molecular
512.53
Número MDL
MFCD02179638
Rotación óptica
[α] D 20
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
238084-15-6
Fórmula molecular
C29H24N2O7
Peso molecular
512.53
Número MDL
MFCD02179638
Rotación óptica
[α] D 20
Condiciones
Conservar entre 0 y 8 °C.
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

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.

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