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Catalog Number:
47709
CAS Number:
113721-87-2
Ester N -succinimidylique de l'acide 7-amino-4-méthyl-3-coumarinacétique
Purity:
≥ 97%
Synonym(s):
7-amino-4-méthyl-3-coumarinylacétate de N-succinimidyle, AMCA-OSu
Documents
$155.00 /25 mg
Taille
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Informations sur le produit

7-Amino-4-methyl-3-coumarinacetic acid N-succinimidyl ester is a versatile compound widely utilized in bioconjugation and labeling applications. This compound features a coumarin moiety, which is known for its fluorescent properties, making it an excellent choice for researchers in the fields of biochemistry and molecular biology. Its N-succinimidyl ester functionality allows for efficient coupling with amine-containing biomolecules, facilitating the development of targeted probes and therapeutic agents. This compound is particularly useful in the creation of fluorescently labeled antibodies and peptides, enhancing the visualization and tracking of biological processes in live cells.

In addition to its applications in research, 7-Amino-4-methyl-3-coumarinacetic acid N-succinimidyl ester is also valuable in the development of diagnostic assays and drug delivery systems. Its ability to form stable conjugates with proteins and nucleic acids opens up possibilities for innovative therapeutic strategies. Researchers will appreciate its ease of use and the high specificity it offers in labeling applications, making it a preferred choice for those looking to advance their studies in molecular imaging and targeted therapies.

Numéro CAS 
113721-87-2
Formule moléculaire
C16H14N2O6
Poids moléculaire 
330.3
Informations générales
Numéro CAS 
113721-87-2
Formule moléculaire
C16H14N2O6
Poids moléculaire 
330.3
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

7-Amino-4-methyl-3-coumarinacetic acid N-succinimidyl ester is widely utilized in research focused on:

  • Bioconjugation: This compound is commonly used to label biomolecules, such as proteins and antibodies, enhancing their detection in various assays. Its reactive N-succinimidyl ester group allows for efficient coupling to amine-containing molecules.
  • Fluorescent Probes: It serves as a fluorescent probe in cellular imaging. Researchers leverage its fluorescence properties to visualize cellular processes, making it invaluable in cell biology studies.
  • Drug Development: In pharmaceutical research, this compound aids in the development of targeted drug delivery systems. Its ability to conjugate with therapeutic agents can improve drug efficacy and reduce side effects.
  • Diagnostics: The compound plays a role in developing diagnostic tools, particularly in immunoassays. Its labeling capabilities enhance the sensitivity and specificity of tests, crucial for accurate disease detection.
  • Research on Protein Interactions: It is utilized in studies examining protein-protein interactions, helping scientists understand complex biological processes and disease mechanisms.

Citations