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Catalog Number:
21768
CAS Number:
35599-02-1
4-Nitrophenyl-β-D-mannopyranoside
Synonym(s):
4-Nitrophenyl-β-D-mannoside
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Product Information

4-Nitrophenyl-b-D-mannopyranoside is a versatile glycoside that serves as an essential substrate in various biochemical applications, particularly in the study of glycosidases and glycosyltransferases. This compound is recognized for its ability to mimic natural substrates, making it invaluable in enzymatic assays and research focused on carbohydrate metabolism. Its unique structure, featuring a nitrophenyl group, enhances its solubility and reactivity, allowing for efficient interactions in biochemical pathways.

In the pharmaceutical and biotechnology sectors, 4-Nitrophenyl-b-D-mannopyranoside is utilized in the development of glycosylation reactions, which are crucial for the synthesis of complex carbohydrates and glycoproteins. Researchers appreciate its role in high-throughput screening processes, where it aids in identifying enzyme activity and specificity. The compound's stability and compatibility with various reaction conditions further underscore its significance in laboratory settings, making it a preferred choice for professionals seeking reliable and effective tools for carbohydrate research.

Synonyms
4-Nitrophenyl-β-D-mannoside
CAS Number
35599-02-1
Molecular Formula
C12H15NO8
Molecular Weight
301.25
MDL Number
MFCD00067650
PubChem ID
259380
Conditions
Store at 0-8°C
General Information
Synonyms
4-Nitrophenyl-β-D-mannoside
CAS Number
35599-02-1
Molecular Formula
C12H15NO8
Molecular Weight
301.25
MDL Number
MFCD00067650
PubChem ID
259380
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Nitrophenyl-b-D-mannopyranoside is widely utilized in research focused on:

  • Enzyme Activity Assays: This compound serves as a substrate in assays to measure the activity of glycosidases, which are important in various biochemical processes.
  • Carbohydrate Research: It is used in studies investigating carbohydrate metabolism and interactions, helping researchers understand sugar-related diseases.
  • Drug Development: The compound aids in the design of glycosylated drugs, enhancing their stability and bioavailability, which is crucial in pharmaceutical formulations.
  • Biotechnology: It plays a role in the development of biosensors that detect specific enzymes, providing a practical tool for monitoring biological processes.
  • Food Industry: This chemical can be employed in the analysis of glycosidic bonds in food products, contributing to quality control and nutritional assessments.

Citations