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Catalog Number:
21693
CAS Number:
4264-82-8
5-Bromo-4-chloro-3-indolyl-N-acetyl-β-D-glucosaminide
Purity:
≥ 99% (HPLC)
Documents
$134.70 /1G
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Product Information

5-Bromo-4-chloro-3-indolyl-N-acetyl-b-D-glucosaminide is a versatile chemical compound widely utilized in biochemical research and pharmaceutical applications. This compound serves as a valuable substrate in enzyme assays, particularly in studies involving glycosyltransferases and other carbohydrate-active enzymes. Its unique structure, featuring both bromine and chlorine substituents on the indole ring, enhances its reactivity and makes it an effective tool for probing enzyme mechanisms and substrate specificity. Researchers appreciate its ability to facilitate the understanding of glycan biosynthesis and its implications in various biological processes.

In addition to its applications in enzyme studies, this compound has potential uses in the development of novel therapeutics targeting glycan-related diseases. Its compatibility with various biochemical assays allows for easy integration into existing research workflows, making it an essential reagent for laboratories focused on glycobiology and medicinal chemistry. The compound's stability and reactivity profile position it as a superior choice compared to similar compounds, providing researchers with reliable results in their experimental endeavors.

CAS Number
4264-82-8
Purity
≥ 99% (HPLC)
Molecular Formula
C16H18BrClN2O6
Molecular Weight
449.68
MDL Number
MFCD00040631
PubChem ID
3673870
Appearance
White to off-white crystalline powder
Conditions
Store at 0 - 8 °C
General Information
CAS Number
4264-82-8
Purity
≥ 99% (HPLC)
Molecular Formula
C16H18BrClN2O6
Molecular Weight
449.68
MDL Number
MFCD00040631
PubChem ID
3673870
Appearance
White to off-white crystalline powder
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

5-Bromo-4-chloro-3-indolyl-N-acetyl-b-D-glucosaminide is widely utilized in research focused on:

  • Biotechnology: This compound serves as a substrate in enzymatic assays, particularly for studying glycosyltransferases, which are crucial in the development of biopharmaceuticals.
  • Pharmaceutical Development: It is used in drug discovery processes, especially for screening potential inhibitors of specific enzymes, aiding in the identification of new therapeutic agents.
  • Diagnostic Applications: The compound can be employed in the development of diagnostic tests, particularly in detecting bacterial infections by targeting specific glycosylation patterns.
  • Research in Cancer Biology: It has applications in cancer research, where it helps in understanding the role of glycosylation in tumor progression and metastasis.
  • Food Industry: This chemical is also explored for its potential use in food safety testing, particularly in detecting glycosylated toxins or pathogens.

Citations