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Catalog Number:
01931
CAS Number:
10357-27-4
4-Nitrofenil-α-D-mano-piranósido
Purity:
≥ 98 % (HPLC)
Synonym(s):
p- Nitrofenil α-D-manopiranósido
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Product Information

4-Nitrophenyl-α-D-manno-pyranoside is a versatile glycoside that serves as a valuable tool in biochemical research and various industrial applications. This compound is recognized for its role as a substrate in enzyme assays, particularly in studies involving glycosidases. Its unique structure, featuring a nitrophenyl group, enhances its reactivity and makes it an effective chromogenic substrate, allowing for easy monitoring of enzymatic activity. Researchers utilize this compound to investigate carbohydrate metabolism and enzyme kinetics, providing insights into biological processes and potential therapeutic targets.

In addition to its applications in enzymology, 4-Nitrophenyl-α-D-manno-pyranoside is also employed in the synthesis of more complex carbohydrate derivatives, contributing to the development of glycomimetics and other bioactive compounds. Its stability and solubility in aqueous solutions make it suitable for various laboratory settings, ensuring reliable results in experimental protocols. With its broad range of applications, this compound is an essential resource for researchers and professionals in the fields of biochemistry, pharmaceuticals, and biotechnology.

Synonyms
p- Nitrofenil α-D-manopiranósido
CAS Number
10357-27-4
Purity
≥ 98 % (HPLC)
Molecular Formula
C12H15Nº8
Molecular Weight
301.3
MDL Number
MFCD00066002
PubChem ID
259380
Appearance
Polvo blanquecino
Conditions
Conservar a ≤ -4 °C
General Information
Synonyms
p- Nitrofenil α-D-manopiranósido
CAS Number
10357-27-4
Purity
≥ 98 % (HPLC)
Molecular Formula
C12H15Nº8
Molecular Weight
301.3
MDL Number
MFCD00066002
PubChem ID
259380
Appearance
Polvo blanquecino
Conditions
Conservar a ≤ -4 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Nitrophenyl-a-D-manno-pyranoside is widely utilized in research focused on:

  • Enzyme Substrates: This compound serves as a substrate for various glycosidases, enabling researchers to study enzyme kinetics and mechanisms in carbohydrate metabolism.
  • Biochemical Assays: It is commonly used in assays to measure enzyme activity, particularly in the fields of biochemistry and molecular biology, providing a reliable method for quantifying enzyme function.
  • Drug Development: The compound's structure allows for modifications that can lead to the development of new therapeutic agents, particularly in targeting glycosylation processes in diseases.
  • Fluorescent Probes: Its nitrophenyl group can be utilized in creating fluorescent probes for imaging studies, enhancing the visualization of biological processes in live cells.
  • Research on Glycoproteins: It aids in the study of glycoprotein interactions and functions, which is crucial for understanding various biological pathways and disease mechanisms.

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