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Catalog Number:
09729
CAS Number:
3459-18-5
p-Nitrophenyl-β-D-N-acetyl-glucosaminide
Purity:
≥ 99% (HPLC)
Synonym(s):
4-Nitrophenyl-2-acetamido-2-deoxy-β-D-glucopyranoside
Temperature Sensitive
Documents
$25.00 /100MG
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Product Information

<p>p-Nitrophenyl-b-D-N-acetyl-glucosaminide is a valuable compound widely utilized in biochemical research and enzyme assays. This substrate is particularly significant for studying glycosidases, as it serves as a chromogenic substrate that enables the detection and quantification of enzyme activity. Its unique structure, featuring a nitrophenyl group, allows for easy monitoring of hydrolysis reactions, making it an essential tool in enzymology and carbohydrate chemistry. Researchers appreciate its high sensitivity and specificity, which facilitate accurate measurements in various experimental setups.</p>

<p>Additionally, p-Nitrophenyl-b-D-N-acetyl-glucosaminide has applications in the development of diagnostic assays and in the pharmaceutical industry for drug development. Its ability to mimic natural substrates makes it an ideal candidate for screening potential inhibitors of glycosidases, which are crucial in various biological processes. By incorporating this compound into their research, scientists can gain insights into enzyme mechanisms and explore therapeutic avenues for diseases related to glycosylation disorders.</p>

Synonyms
4-Nitrophenyl-2-acetamido-2-deoxy-β-D-glucopyranoside
CAS Number
3459-18-5
Purity
≥ 99% (HPLC)
Molecular Formula
C14H18N2O8
Molecular Weight
342.3
MDL Number
MFCD00063696
PubChem ID
558756
Appearance
Off-white powder
Conditions
Store at -10°
General Information
Synonyms
4-Nitrophenyl-2-acetamido-2-deoxy-β-D-glucopyranoside
CAS Number
3459-18-5
Purity
≥ 99% (HPLC)
Molecular Formula
C14H18N2O8
Molecular Weight
342.3
MDL Number
MFCD00063696
PubChem ID
558756
Appearance
Off-white powder
Conditions
Store at -10°
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

p-Nitrophenyl-b-D-N-acetyl-glucosaminide is widely utilized in research focused on:

  • Enzyme Activity Assays: This compound serves as a substrate for various glycosidases, allowing researchers to study enzyme kinetics and mechanisms in carbohydrate metabolism.
  • Biochemical Research: It is used in studies related to glycoprotein synthesis and modification, providing insights into cellular processes and disease mechanisms.
  • Drug Development: The compound aids in the screening of potential inhibitors for glycosidases, which can be crucial in developing treatments for diseases like cancer and diabetes.
  • Diagnostic Applications: It can be employed in assays to detect specific enzyme activities in clinical samples, helping in the diagnosis of metabolic disorders.
  • Educational Purposes: This chemical is often used in laboratory settings for teaching students about enzyme-substrate interactions and carbohydrate chemistry.

Citations