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Catalog Number:
07926
CAS Number:
83701-04-6
Nα-Benzoyl-L-arginine 7-amido-4-methylcoumarin hydrochloride
Synonym(s):
Bz-L-Arg-AMC·HCl
Documents
$148.22 /50MG
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Product Information

Na-Benzoyl-L-arginine 7-amido-4-methylcoumarin hydrochloride is a versatile compound widely utilized in biochemical research and pharmaceutical applications. This compound is particularly valued for its role as a substrate in enzyme assays, especially in studies involving proteases and peptidases. Its unique structure, featuring a benzoyl group and a 7-amido-4-methylcoumarin moiety, allows for effective fluorescence-based detection, making it an excellent choice for researchers seeking to monitor enzymatic activity in real-time.

In addition to its applications in enzyme assays, Na-Benzoyl-L-arginine 7-amido-4-methylcoumarin hydrochloride is also employed in the development of therapeutic agents and in the study of protein interactions. Its ability to provide clear fluorescence signals enhances its utility in high-throughput screening processes, facilitating the discovery of new drugs and biological pathways. Researchers and industry professionals will appreciate its reliability and effectiveness in various experimental setups, making it a valuable addition to any laboratory focused on biochemical analysis.

Synonyms
Bz-L-Arg-AMC·HCl
CAS Number
83701-04-6
Molecular Formula
C23H25N5O4·HCl
Molecular Weight
471.94
MDL Number
MFCD00039020
PubChem ID
16219048
Conditions
Store at 0-8°C
General Information
Synonyms
Bz-L-Arg-AMC·HCl
CAS Number
83701-04-6
Molecular Formula
C23H25N5O4·HCl
Molecular Weight
471.94
MDL Number
MFCD00039020
PubChem ID
16219048
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na-Benzoyl-L-arginine 7-amido-4-methylcoumarin hydrochloride is widely utilized in research focused on:

  • Biochemical Assays: This compound serves as a substrate in enzyme assays, particularly for studying proteases. Its unique structure allows for specific interactions, providing clear results in enzyme activity measurements.
  • Fluorescent Labeling: The fluorescent properties of this compound make it ideal for labeling biomolecules in live-cell imaging, enabling researchers to track cellular processes in real-time.
  • Drug Development: Used in the development of novel therapeutic agents, it helps in screening potential drug candidates due to its ability to mimic biological substrates, facilitating the identification of effective compounds.
  • Diagnostic Applications: Its specificity in biochemical reactions allows for the development of diagnostic tests, particularly in identifying protease-related diseases, enhancing early detection and treatment strategies.
  • Research on Protein Interactions: This compound aids in studying protein-protein interactions, providing insights into cellular mechanisms and pathways, which is crucial for understanding disease progression and treatment options.

Citations