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Catalog Number:
21308
CAS Number:
5609-91-6
5-Bromo-6-chloro-3-indoxyl-N-acetyl-ॆ-D-glucosaminide
Synonym(s):
5-Bromo-6-chloro-3-indolyl-N-acetyl-β-D-glucosaminide, 5-Bromo-6-chloro-3-indoxyl-2-acetamido-2-deoxy-β-D-glucopyranoside
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Product Information

5-Bromo-6-chloro-3-indoxyl-N-acetyl-b-D-glucosaminide is a specialized chemical compound that serves as a valuable substrate in various biochemical applications. This compound is particularly recognized for its role in enzymatic assays, where it acts as a chromogenic substrate for the detection of specific glycosidases. Its unique structure, featuring both bromine and chlorine substituents, enhances its reactivity and specificity, making it an ideal choice for researchers looking to study enzyme kinetics and carbohydrate metabolism.

In addition to its applications in enzymatic assays, this compound is also utilized in histochemical staining techniques, providing researchers with a reliable method for visualizing enzyme activity in tissue samples. The ability to produce a distinct color change upon enzymatic reaction allows for easy identification and quantification, which is crucial in both clinical and research settings. With its robust performance and versatility, 5-Bromo-6-chloro-3-indoxyl-N-acetyl-b-D-glucosaminide stands out as a preferred choice for professionals in biochemistry and molecular biology.

Synonyms
5-Bromo-6-chloro-3-indolyl-N-acetyl-β-D-glucosaminide, 5-Bromo-6-chloro-3-indoxyl-2-acetamido-2-deoxy-β-D-glucopyranoside
CAS Number
5609-91-6
Molecular Formula
C16H18BrClN2O6
Molecular Weight
449.68
MDL Number
MFCD00798384
PubChem ID
22345919
Conditions
Store at 0-8°C
General Information
Synonyms
5-Bromo-6-chloro-3-indolyl-N-acetyl-β-D-glucosaminide, 5-Bromo-6-chloro-3-indoxyl-2-acetamido-2-deoxy-β-D-glucopyranoside
CAS Number
5609-91-6
Molecular Formula
C16H18BrClN2O6
Molecular Weight
449.68
MDL Number
MFCD00798384
PubChem ID
22345919
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-6-chloro-3-indoxyl-N-acetyl-b-D-glucosaminide is widely utilized in research focused on:

  • Enzyme Substrates: This compound serves as a substrate for various enzymes, allowing researchers to study enzyme activity and kinetics in biochemical assays.
  • Histochemical Staining: It is used in histochemistry for visualizing specific cellular components, aiding in the identification of tissue types and disease states.
  • Biotechnology Applications: The compound is valuable in genetic engineering and molecular biology, particularly in the development of biosensors and reporter systems.
  • Pharmaceutical Research: It plays a role in drug discovery processes, where it can be utilized to screen for potential therapeutic agents targeting specific biological pathways.
  • Diagnostic Tools: This chemical is incorporated into diagnostic kits for detecting certain diseases, enhancing the accuracy and efficiency of medical testing.

Citations