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Catalog Number:
20986
CAS Number:
117153-55-6
4-(trifluorométhyl)umbelliféryl-β-D-galactopyranoside
Synonym(s):
TFMU-Gal
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Product Information

4-(Trifluoromethyl)umbelliferyl-b-D-galactopyranoside is a specialized chemical compound that serves as a valuable substrate in biochemical research and applications. This compound is particularly recognized for its role in glycosidase assays, where it acts as a fluorogenic substrate, allowing for the sensitive detection of enzyme activity. The trifluoromethyl group enhances its stability and solubility, making it an ideal choice for various laboratory settings. Researchers utilize this compound in studies related to carbohydrate metabolism, enzyme kinetics, and the development of glycosylation processes in pharmaceuticals.

In addition to its utility in enzyme assays, 4-(Trifluoromethyl)umbelliferyl-b-D-galactopyranoside can be employed in the synthesis of glycosylated compounds, which are crucial in drug development and therapeutic applications. Its unique properties facilitate the exploration of glycosylation patterns, aiding in the design of novel glycosylated drugs with improved efficacy and reduced side effects. This compound stands out due to its enhanced detection capabilities and versatility in various biochemical applications, making it an essential tool for researchers and industry professionals alike.

Synonyms
TFMU-Gal
CAS Number
117153-55-6
Molecular Formula
C 16 H 15 F 3 O 8
Molecular Weight
392.28
MDL Number
MFCD00064056
PubChem ID
4118071
Conditions
Conserver à 0-8°C
General Information
Synonyms
TFMU-Gal
CAS Number
117153-55-6
Molecular Formula
C 16 H 15 F 3 O 8
Molecular Weight
392.28
MDL Number
MFCD00064056
PubChem ID
4118071
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4-(Trifluoromethyl)umbelliferyl-b-D-galactopyranoside is widely utilized in research focused on:

  • Enzyme Activity Assays: This compound serves as a substrate for various glycosidases, allowing researchers to measure enzyme activity in biochemical assays effectively.
  • Fluorescent Probes: Its unique structure makes it suitable for use as a fluorescent probe in cellular imaging, helping scientists visualize biological processes in real-time.
  • Carbohydrate Research: The compound is valuable in studying carbohydrate metabolism and interactions, providing insights into glycosylation processes in cells.
  • Drug Development: It is used in the development of new pharmaceuticals targeting glycosidase enzymes, which play a crucial role in various diseases, including cancer and diabetes.
  • Biotechnology Applications: The compound is applied in biotechnological processes, such as enzyme engineering and synthetic biology, enhancing the efficiency of biocatalysts.

Citations