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Catalog Number:
21146
CAS Number:
53643-12-2
4-Methylumbelliferyl β-D-N,N-diacetyl-chitobioside
Synonym(s):
[(4-Methylumbelliferyl)-N-acetylglucosamine]-4,1-N-acetylglucosamine, 4-Methylumbelliferyl-N,N-diacetyl-β-D-chitobioside, N,N-Diacetyl-4-methylumbelliferyl-β-D-chitobioside
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Product Information

4-Methylumbelliferyl b-D-N,N'-diacetyl-chitobioside is a specialized substrate widely utilized in biochemical research, particularly in the study of glycosidases and glycosyltransferases. This compound serves as an effective fluorogenic substrate, enabling researchers to monitor enzymatic activity through fluorescence. Its unique structure, featuring a 4-methylumbelliferyl moiety, allows for sensitive detection, making it an invaluable tool in enzymology and carbohydrate chemistry.

In practical applications, this compound is often employed in assays to evaluate the activity of enzymes involved in carbohydrate metabolism, which is crucial for understanding various biological processes and disease mechanisms. Its ability to provide real-time data on enzyme kinetics enhances the efficiency of research, facilitating advancements in drug development and therapeutic interventions. Researchers appreciate its high specificity and sensitivity, which set it apart from other substrates, ensuring reliable results in complex biological samples.

Synonyms
[(4-Methylumbelliferyl)-N-acetylglucosamine]-4,1-N-acetylglucosamine, 4-Methylumbelliferyl-N,N-diacetyl-β-D-chitobioside, N,N-Diacetyl-4-methylumbelliferyl-β-D-chitobioside
CAS Number
53643-12-2
Molecular Formula
C26H34N2O13
Molecular Weight
582.56
MDL Number
MFCD00082499
PubChem ID
4185783
Conditions
Store at 0-8°C
General Information
Synonyms
[(4-Methylumbelliferyl)-N-acetylglucosamine]-4,1-N-acetylglucosamine, 4-Methylumbelliferyl-N,N-diacetyl-β-D-chitobioside, N,N-Diacetyl-4-methylumbelliferyl-β-D-chitobioside
CAS Number
53643-12-2
Molecular Formula
C26H34N2O13
Molecular Weight
582.56
MDL Number
MFCD00082499
PubChem ID
4185783
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

4-Methylumbelliferyl b-D-N,N'-diacetyl-chitobioside is widely utilized in research focused on:

  • Enzyme Activity Assays: This compound serves as a substrate in assays to measure the activity of specific enzymes, particularly glycosidases, allowing researchers to quantify enzyme kinetics effectively.
  • Fluorescent Labeling: Its fluorescent properties enable it to be used in various labeling applications, enhancing the visualization of biomolecules in microscopy and flow cytometry.
  • Biochemical Research: It plays a crucial role in studying carbohydrate metabolism and glycoprotein interactions, providing insights into cellular processes and disease mechanisms.
  • Drug Development: The compound is valuable in screening potential drug candidates that target glycosylation pathways, which are important in many therapeutic areas, including cancer and infectious diseases.
  • Quality Control in Biotechnology: It is utilized in the quality assessment of biopharmaceuticals, ensuring that glycosylation patterns are consistent and meet regulatory standards.

Citations