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Catalog Number:
21411
CAS Number:
156117-44-1
6-Chloro-3-indoxyl-N-acetyl-β-D-glucosaminide
Synonym(s):
6-Chloro-3-indolyl N-acetyl-β-D-glucosaminide, 6-Chloro-3-(2-acetamido-2-deoxy-β-D-glucopyranosyloxy)indole
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Product Information

6-Chloro-3-indoxyl-N-acetyl-b-D-glucosaminide is a specialized compound that plays a significant role in biochemical research and applications. This compound is particularly valued for its use as a substrate in enzyme assays, especially in studies involving glycosyltransferases and other carbohydrate-active enzymes. Its unique structure allows for the selective detection of enzymatic activity, making it an essential tool in the development of diagnostic assays and in the study of metabolic pathways. Researchers appreciate its ability to provide clear, quantifiable results, which can enhance the understanding of enzyme kinetics and substrate specificity.

In addition to its applications in enzyme assays, 6-Chloro-3-indoxyl-N-acetyl-b-D-glucosaminide is also utilized in the synthesis of various bioactive compounds. Its versatility in chemical reactions makes it a valuable intermediate in the pharmaceutical and biotechnology industries. The compound's stability and reactivity under various conditions further enhance its appeal for researchers looking to develop new therapeutic agents or study complex biochemical processes. Overall, this compound stands out for its practical applications in both academic and industrial settings, offering significant benefits to professionals in the field.

Synonyms
6-Chloro-3-indolyl N-acetyl-β-D-glucosaminide, 6-Chloro-3-(2-acetamido-2-deoxy-β-D-glucopyranosyloxy)indole
CAS Number
156117-44-1
Molecular Formula
C16H19ClN2O6
Molecular Weight
370.79
MDL Number
MFCD04972051
PubChem ID
22345917
Conditions
Store at 0-8°C
General Information
Synonyms
6-Chloro-3-indolyl N-acetyl-β-D-glucosaminide, 6-Chloro-3-(2-acetamido-2-deoxy-β-D-glucopyranosyloxy)indole
CAS Number
156117-44-1
Molecular Formula
C16H19ClN2O6
Molecular Weight
370.79
MDL Number
MFCD04972051
PubChem ID
22345917
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

6-Chloro-3-indoxyl-N-acetyl-b-D-glucosaminide is widely utilized in research focused on:

  • Biochemical Assays: This compound serves as a substrate in various enzymatic assays, allowing researchers to study enzyme activity and kinetics effectively.
  • Drug Development: It plays a role in the synthesis of potential pharmaceutical agents, particularly in targeting specific biological pathways, which can lead to the development of new therapies.
  • Diagnostics: The compound is used in diagnostic tests, particularly in identifying certain bacterial infections by acting as a chromogenic substrate.
  • Cell Biology: It is applied in cell culture studies to investigate cellular processes, including glycosylation patterns and their effects on cell function.
  • Research on Glycobiology: This chemical aids in the exploration of carbohydrate-protein interactions, providing insights into cellular communication and signaling mechanisms.

Citations