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Catalog Number:
08675
CAS Number:
115035-46-6
H-Gly-Pro-AMC·HBr
Temperature Sensitive
Documents
$113.70 /5MG
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Product Information

H-Gly-Pro-AMC·HBr is a specialized compound widely utilized in biochemical research and pharmaceutical applications. This hydrobromide salt of H-Gly-Pro-AMC serves as a valuable substrate in protease assays, particularly for studying enzyme kinetics and inhibition. Its unique structure, featuring a chromen-7-yl moiety, enhances its specificity and sensitivity, making it an ideal choice for researchers investigating proteolytic activity. The compound's ability to release a fluorescent signal upon cleavage allows for real-time monitoring of enzyme activity, facilitating high-throughput screening in drug discovery processes.

Moreover, H-Gly-Pro-AMC·HBr is recognized for its stability and solubility in various biological buffers, which is crucial for experimental consistency. Its application extends beyond basic research, as it can also be employed in the development of therapeutic agents targeting protease-related diseases. By incorporating this compound into your research toolkit, you can enhance the accuracy and efficiency of your experiments, paving the way for innovative discoveries in biochemistry and pharmacology.

CAS Number
115035-46-6
Molecular Formula
C17H19N3O4·HBr
Molecular Weight
410.27
MDL Number
MFCD00152092
PubChem ID
16219396
Conditions
Store at -0°C.
General Information
CAS Number
115035-46-6
Molecular Formula
C17H19N3O4·HBr
Molecular Weight
410.27
MDL Number
MFCD00152092
PubChem ID
16219396
Conditions
Store at -0°C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

H-Gly-Pro-AMC·HBr is widely utilized in research focused on:

  • Biochemical Assays: This compound serves as a substrate in enzyme assays, particularly for proteases, enabling researchers to study enzyme kinetics and mechanisms.
  • Drug Development: It is used in the screening of potential drug candidates, allowing pharmaceutical companies to evaluate the efficacy of new compounds against specific biological targets.
  • Peptide Synthesis: H-Gly-Pro-AMC·HBr is valuable in the synthesis of peptides, facilitating the creation of custom peptides for various applications in research and therapeutics.
  • Fluorescent Probes: The compound can be utilized in developing fluorescent probes for imaging studies, helping researchers visualize biological processes in real-time.
  • Diagnostic Applications: It has potential in diagnostic assays, particularly in identifying specific biomarkers in diseases, enhancing the accuracy of disease detection.

Citations