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Catalog Number:
06063
CAS Number:
113728-13-5
Glycine 7-amido-4-methylcoumarin hydrobromide
Purity:
≥ 98% (Assay)
Synonym(s):
Gly-AMC·HBr
Documents
$110.00 /100MG
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Product Information

Glycine 7-amido-4-methylcoumarin hydrobromide is a versatile compound widely recognized for its applications in biochemical research and fluorescence studies. This compound, a derivative of glycine and 4-methylcoumarin, exhibits unique fluorescent properties that make it an excellent choice for use in assays and imaging techniques. Its ability to act as a substrate for various enzymes allows researchers to explore enzyme kinetics and mechanisms effectively. Additionally, its hydrobromide form enhances its solubility in aqueous solutions, facilitating its use in biological systems.

In the pharmaceutical and biochemical industries, Glycine 7-amido-4-methylcoumarin hydrobromide is particularly valuable for developing fluorescent probes and markers. Its specific structure enables it to be utilized in the detection of proteases and other enzymes, providing insights into cellular processes and disease mechanisms. Researchers appreciate its stability and ease of use, making it a preferred choice for laboratory applications. With its unique properties, this compound holds significant potential for advancing research in enzymology and molecular biology.

Synonyms
Gly-AMC·HBr
CAS Number
113728-13-5
Purity
≥ 98% (Assay)
Molecular Formula
C12H12N2O3·HBr
Molecular Weight
313.16
MDL Number
MFCD00058452
PubChem ID
2733763
Appearance
White to off-white powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Gly-AMC·HBr
CAS Number
113728-13-5
Purity
≥ 98% (Assay)
Molecular Formula
C12H12N2O3·HBr
Molecular Weight
313.16
MDL Number
MFCD00058452
PubChem ID
2733763
Appearance
White to off-white powder
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

Glycine 7-amido-4-methylcoumarin hydrobromide is widely utilized in research focused on:

  • Fluorescent Probes: This compound serves as a fluorescent probe in biochemical assays, allowing researchers to track cellular processes and interactions with high sensitivity.
  • Enzyme Activity Studies: It is used to study enzyme kinetics, particularly in the assessment of protease activity, providing insights into enzyme mechanisms and potential inhibitors.
  • Drug Development: The compound plays a role in the development of new pharmaceuticals, especially in targeting specific biological pathways, enhancing therapeutic efficacy.
  • Biochemical Research: It is valuable in various biochemical experiments, including the study of protein interactions and cellular signaling pathways, aiding in the understanding of complex biological systems.
  • Diagnostic Applications: This chemical is also explored for use in diagnostic assays, improving the detection of certain biomarkers in clinical settings, which can lead to better patient outcomes.

Citations