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Catalog Number:
20946
CAS Number:
65174-63-2
1-Naphthyl-α-D-galactopyranoside
Synonym(s):
α-naphtyl-α-galactoside
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Product Information

1-Naphthyl-a-D-galactopyranoside is a versatile glycoside that serves as a valuable substrate in various biochemical applications. This compound is widely recognized for its role in enzyme assays, particularly in the study of glycosidases, where it acts as a chromogenic substrate. Upon hydrolysis by specific enzymes, it releases a naphthol derivative that can be easily detected, making it an essential tool for researchers in enzymology and carbohydrate chemistry. Its unique structure not only enhances its reactivity but also allows for selective interactions with various enzymes, providing insights into enzyme kinetics and mechanisms.

In addition to its applications in research, 1-Naphthyl-a-D-galactopyranoside is also utilized in the development of biosensors and diagnostic assays, where its ability to produce measurable signals upon enzymatic action is crucial. The compound's stability and ease of use make it a preferred choice for laboratories focused on carbohydrate metabolism studies and related fields. With its significant role in advancing scientific knowledge, this compound is an indispensable asset for researchers and industry professionals alike.

Synonyms
α-naphtyl-α-galactoside
CAS Number
65174-63-2
Molecular Formula
C16H18O6
Molecular Weight
306.31
MDL Number
MFCD00067611
PubChem ID
2844794
Conditions
Conserver à 0-8°C
General Information
Synonyms
α-naphtyl-α-galactoside
CAS Number
65174-63-2
Molecular Formula
C16H18O6
Molecular Weight
306.31
MDL Number
MFCD00067611
PubChem ID
2844794
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

1-Naphthyl-a-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, which is crucial for understanding metabolic pathways.
  • Cell Biology Studies: It is used in cell culture to study cell signaling and carbohydrate recognition, providing insights into cellular interactions and functions.
  • Drug Development: The compound aids in the screening of potential drug candidates by evaluating their effects on glycosylation processes, which are important in pharmacology.
  • Biochemical Research: It helps in the investigation of carbohydrate-binding proteins, contributing to the development of targeted therapies and diagnostic tools in medicine.
  • Food Industry Applications: The compound is utilized in food science to study the effects of glycosylation on flavor and texture, enhancing product development and quality control.

Citations