🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
21217
CAS Number:
1226-39-7
4-Nitrofenil-β-D-fucopiranósido
Synonym(s):
4-Nitrofenil-β-D-fucosa, p- Nitrofenil-β-D-fucósido
Documents
Available - Request Bulk Quote
Tamaño
Request Bulk Quote
Product Information

4-Nitrophenyl-β-D-fucopyranoside is a versatile glycoside that serves as a valuable substrate in various biochemical applications, particularly in the study of glycosidases and carbohydrate-active enzymes. This compound is recognized for its ability to facilitate the understanding of enzyme kinetics and mechanisms, making it an essential tool for researchers in the fields of biochemistry and molecular biology. Its unique structure, featuring a nitrophenyl group, enhances its reactivity and allows for the development of sensitive assays, which are crucial for detecting and quantifying enzyme activity.

In addition to its research applications, 4-Nitrophenyl-β-D-fucopyranoside is also utilized in the synthesis of complex carbohydrates and glycoproteins, contributing to advancements in glycoscience. Its compatibility with various analytical techniques, such as HPLC and mass spectrometry, further underscores its importance in both academic and industrial settings. By providing a reliable means to study enzyme interactions and carbohydrate structures, this compound holds significant potential for innovations in drug development and therapeutic research.

Synonyms
4-Nitrofenil-β-D-fucosa, p- Nitrofenil-β-D-fucósido
CAS Number
1226-39-7
Molecular Formula
C12H15Nº7
Molecular Weight
285.25
MDL Number
MFCD00040651
PubChem ID
3388422
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
4-Nitrofenil-β-D-fucosa, p- Nitrofenil-β-D-fucósido
CAS Number
1226-39-7
Molecular Formula
C12H15Nº7
Molecular Weight
285.25
MDL Number
MFCD00040651
PubChem ID
3388422
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Nitrophenyl-b-D-fucopyranoside 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 and kinetics in carbohydrate metabolism studies.
  • Carbohydrate Research: It is instrumental in the study of fucosylation processes, aiding in the understanding of cell signaling and recognition mechanisms in biological systems.
  • Biotechnology Applications: In the development of biosensors, it can be used to detect specific glycosylation patterns, which is crucial for quality control in biopharmaceutical production.
  • Drug Development: The compound's role in glycosylation pathways makes it valuable in the design of glycomimetics, which can enhance the efficacy of therapeutic agents.
  • Educational Purposes: It is commonly used in academic laboratories to teach students about enzymatic reactions and carbohydrate chemistry, providing hands-on experience with real-world applications.

Citas