Product Name
6-Methyl-2-pyridinyl 2-(acetylamino)-2-deoxy-1-thio-β-D-glucopyranoside, 98%
Certificate of Analysis (COA)
Product Introduction
6-Methyl-2-pyridinyl 2-(acetylamino)-2-deoxy-1-thio-β-D-glucopyranoside (MUGS derivative) is a synthetic chromogenic or fluorogenic substrate analog commonly used for glycosidase and glycosyl hydrolase activity studies, particularly enzymes involved in N-acetylglucosamine metabolism.
The compound contains a 2-acetamido-2-deoxy-β-D-glucopyranoside moiety linked through a thioglycosidic bond to a substituted pyridine group, making it suitable for enzymatic cleavage by N-acetyl-β-D-glucosaminidases and related glycosidases.
Upon enzymatic hydrolysis, the substrate releases a pyridinyl chromophore or detectable product, enabling spectrophotometric or fluorometric monitoring of enzyme activity. Because of this property, the compound is widely used in glycosidase assays, carbohydrate metabolism research, enzymology studies, and biochemical screening assays.
Mechanism of Reaction
6-Methyl-2-pyridinyl 2-(acetylamino)-2-deoxy-1-thio-β-D-glucopyranoside functions as a synthetic glycosidase substrate.During the enzymatic reaction:
- Glycosidase enzymes recognize the β-D-glucosaminide structure
- The enzyme cleaves the thioglycosidic linkage
- A detectable pyridinyl-containing product is released
- The reaction can be monitored through spectrophotometric or fluorometric detection
The increase in signal intensity correlates with glycosidase activity in the sample.
Key Research Applications
1.Glycosidase Activity Assays
This compound is frequently used for quantitative determination of glycosidase activity, especially enzymes involved in N-acetylglucosamine metabolism.Typical applications include:
- N-acetyl-β-D-glucosaminidase activity assays
- Glycosyl hydrolase enzyme studies
- Enzyme activity monitoring
2.Carbohydrate Metabolism Research
The substrate is widely used in studies investigating carbohydrate metabolism and glycan processing pathways.Applications include:
- Glycan degradation studies
- Carbohydrate metabolic pathway analysis
- Glycosidase functional characterization
3.Enzyme Kinetics Studies
The compound is suitable for enzyme kinetics experiments involving glycosidases.Typical uses include:
- Determination of kinetic parameters (Km and Vmax)
- Substrate specificity studies
- Comparative enzyme activity analysis
4.Pharmaceutical and Diagnostic Research
Because glycosidases are involved in many biological processes, this compound is also used in drug discovery and biochemical assay development.Applications include:
- Glycosidase inhibitor screening
- Enzyme-targeted drug discovery
- Diagnostic enzyme assay development
Recommended Experimental Conditions
| Parameter |
Recommended Conditions |
| Detection Method |
Spectrophotometric or fluorometric detection |
| Detection Wavelength |
Typically 340–405 nm depending on assay design |
| Buffer Systems |
Phosphate buffer, Tris-HCl buffer, or acetate buffer |
| Temperature |
25–37 °C |
| Assay Format |
Spectrophotometric assays, fluorometric assays, microplate assays |
Optimization may be required depending on enzyme source and assay conditions.
Advantages in Enzyme Assays
- Synthetic substrate for glycosidase enzyme studies
- Suitable for spectrophotometric or fluorometric detection
- Compatible with microplate-based enzyme assays
- Useful for enzyme kinetics and inhibitor screening studies
Storage & Handling
Non-combustible solids that cannot be assigned to any of the above
storage classes
Research Areas
Researchers working in the following fields may benefit from this compound:
- Glycobiology and carbohydrate research
- Enzymology and enzyme kinetics
- Glycosidase enzyme studies
- Molecular and cellular biology
- Pharmaceutical and biochemical research
What is 6-Methyl-2-pyridinyl 2-(acetylamino)-2-deoxy-1-thio-β-D-glucopyranoside used for?
It is commonly used as a synthetic substrate for glycosidase activity assays, particularly enzymes involved in N-acetylglucosamine metabolism.
What types of enzymes can cleave this substrate?
Enzymes such as N-acetyl-β-D-glucosaminidases and related glycosyl hydrolases can hydrolyze the glycosidic bond.
Why is this compound useful in enzyme assays?
Because it allows convenient detection of enzymatic activity through spectrophotometric or fluorometric measurements.