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Catalog Number:
21003
CAS Number:
177966-52-8
5-Bromo-4-chloro-3-indolyl β-D-cellobioside
Synonym(s):
X-β-D-cellobioside
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Product Information

5-Bromo-4-chloro-3-indolyl β-D-cellobioside is a specialized compound widely recognized for its applications in biochemical research and molecular biology. This compound serves as a valuable substrate in the study of glycosylation processes and enzyme activity, particularly in the context of glycosidases. Its unique structure, featuring both bromine and chlorine substituents, enhances its reactivity and specificity, making it an ideal choice for researchers investigating carbohydrate metabolism and enzyme interactions.

In practical applications, 5-Bromo-4-chloro-3-indolyl β-D-cellobioside is utilized in assays to monitor enzymatic activity and to explore the mechanisms of glycosylation in various biological systems. Its ability to act as a chromogenic substrate allows for easy detection and quantification, providing researchers with a reliable tool for studying enzyme kinetics and substrate specificity. This compound is particularly advantageous in comparative studies, where its distinct halogenated structure can yield insights into the behavior of similar glycosides, thereby facilitating advancements in the field of glycobiology.

Synonyms
X-β-D-cellobioside
CAS Number
177966-52-8
Molecular Formula
C20H25BrClNO11
Molecular Weight
570.77
MDL Number
MFCD00798387
PubChem ID
42609172
Conditions
Store at 0-8°C
General Information
Synonyms
X-β-D-cellobioside
CAS Number
177966-52-8
Molecular Formula
C20H25BrClNO11
Molecular Weight
570.77
MDL Number
MFCD00798387
PubChem ID
42609172
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 b-D-cellobioside is widely utilized in research focused on:

  • Plant Biotechnology: This compound serves as a substrate for detecting β-glucosidase activity, which is crucial in studying plant metabolism and genetic engineering.
  • Drug Development: It is used in screening assays to identify compounds that can inhibit specific enzymes, aiding in the discovery of new pharmaceuticals.
  • Microbial Research: The chemical is employed in studies involving microbial fermentation processes, helping researchers understand how microorganisms break down complex carbohydrates.
  • Food Industry: It can be used to assess the enzymatic activity in food processing, particularly in the production of bioactive compounds from plant materials.
  • Environmental Science: This compound is utilized in research to monitor soil health by studying the enzymatic activities of soil microorganisms, which are vital for nutrient cycling.

Citations