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Catalog Number:
47709
CAS Number:
113721-87-2
Éster N -succinimidílico del ácido 7-amino-4-metil-3-cumarinacético
Purity:
≥ 97%
Synonym(s):
7-amino-4-metil-3-cumarinilacetato de N-succinimidilo, AMCA-OSu
Documents
$155.00 /25 mg
Tamaño
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Información del producto

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.

Número CAS
113721-87-2
Fórmula molecular
C16H14N2O6
Peso molecular
330.3
Número MDL
MFCD00036170
Condiciones
Conservar entre 2 y 8 °C.
Información general
Número CAS
113721-87-2
Fórmula molecular
C16H14N2O6
Peso molecular
330.3
Número MDL
MFCD00036170
Condiciones
Conservar entre 2 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
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Aplicaciones

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.

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