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Catalog Number:
21350
CAS Number:
76204-02-9
2'-(4-Methylumbelliferyl)-α-D-N-acetylneuraminic acid sodium salt
Synonym(s):
4-Mu-Nana Na
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Product Information

2'-(4-Methylumbelliferyl)-α-D-N-acetylneuraminic acid sodium salt is a specialized compound widely utilized in biochemical research and diagnostics. This sodium salt derivative of N-acetylneuraminic acid is particularly valued for its role as a substrate in enzyme assays, especially for sialidases, which are critical in various biological processes including cell signaling and pathogen interactions. Its unique structure, featuring a fluorescent 4-methylumbelliferyl moiety, allows for easy detection and quantification, making it an essential tool in enzymatic studies and molecular biology applications.

Researchers in the fields of glycoscience and microbiology can leverage this compound for studying glycoprotein interactions and the enzymatic activity of sialidases in various organisms. Its fluorescent properties not only facilitate real-time monitoring of enzymatic reactions but also enhance sensitivity in assays, providing a significant advantage over traditional substrates. This compound is ideal for laboratories focusing on glycan analysis, vaccine development, and the study of viral infections, where understanding sialic acid metabolism is crucial.

Synonyms
4-Mu-Nana Na
CAS Number
76204-02-9
Molecular Formula
C21H24NO11·Na
Molecular Weight
489.41
MDL Number
MFCD00057309
PubChem ID
4658389
Conditions
Store at 0-8°C
General Information
Synonyms
4-Mu-Nana Na
CAS Number
76204-02-9
Molecular Formula
C21H24NO11·Na
Molecular Weight
489.41
MDL Number
MFCD00057309
PubChem ID
4658389
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

2'-(4-Methylumbelliferyl)-a-D-N-acetylneuraminic acid sodium salt is widely utilized in research focused on:

  • Enzyme Activity Assays: This compound serves as a substrate for sialidase enzymes, allowing researchers to measure enzyme activity in various biological samples, which is crucial for understanding metabolic pathways.
  • Cell Biology: It is used in cell culture studies to investigate the role of sialic acids in cell recognition and signaling, providing insights into cellular interactions and immune responses.
  • Diagnostic Applications: The compound can be employed in diagnostic kits to detect sialidase activity in clinical samples, aiding in the diagnosis of certain diseases, including viral infections.
  • Biotechnology: In the field of biotechnology, it is utilized for the development of sialylated glycoproteins, which are important for vaccine development and therapeutic proteins.
  • Research on Glycobiology: This chemical plays a significant role in glycobiology research, helping scientists understand the structure and function of glycoproteins and their impact on health and disease.

Citations