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Catalog Number:
28985
CAS Number:
94452-17-2
6-Hexadecanoilamido-4-metilumbeliferil β-D-galactopiranósido
Purity:
Punto único
Documents
$210.00 /1 mg
Tamaño
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Product Information

6-Hexadecanoylamido-4-methylumbelliferyl β-D-galactopyranoside is a specialized glycoside that serves as a valuable substrate in enzymatic assays, particularly for the detection of β-galactosidase activity. This compound is characterized by its unique structure, which combines a long-chain fatty acid with a fluorescent moiety, making it an excellent choice for researchers in biochemistry and molecular biology. Its ability to fluoresce upon cleavage by β-galactosidase allows for sensitive and quantitative analysis, facilitating studies in enzyme kinetics and metabolic pathways.

In practical applications, this compound is widely utilized in the development of diagnostic assays and in the study of glycosylation processes in various biological systems. Its specificity and sensitivity make it an indispensable tool for researchers investigating enzyme functions, cellular processes, and the development of therapeutic strategies. The long aliphatic chain enhances membrane permeability, allowing for effective cellular uptake, which is particularly beneficial in drug delivery and bioassay development.

CAS Number
94452-17-2
Purity
Punto único
Molecular Formula
C 32 H 49 N.º 9
Molecular Weight
591.74
MDL Number
MFCD06796945
PubChem ID
13422191
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
94452-17-2
Purity
Punto único
Molecular Formula
C 32 H 49 N.º 9
Molecular Weight
591.74
MDL Number
MFCD06796945
PubChem ID
13422191
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

6-Hexadecanoylamido-4-methylumbelliferyl b-D-galactopyranoside is widely utilized in research focused on:

  • Enzyme Activity Assays: This compound serves as a substrate for specific 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 cellular uptake and metabolism of glycosylated compounds, providing insights into cell signaling and function.
  • Biotechnology: The chemical is applied in the development of biosensors that detect enzyme activity, enhancing the efficiency of diagnostic tools in clinical settings.
  • Pharmaceutical Research: It aids in drug formulation studies, particularly in assessing the stability and bioavailability of glycosylated drugs, which can improve therapeutic outcomes.
  • Food Industry: This compound can be used to study the enzymatic breakdown of carbohydrates in food products, helping to optimize processing methods and improve product quality.

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