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Catalog Number:
21133
CAS Number:
199326-16-4
Sel de cyclohexylammonium de 5-bromo-3-indolyl β-D-glucuronide
Synonym(s):
Sel de glucuronide bleu·CHA
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Product Information

5-Bromo-3-indolyl β-D-glucuronide cyclohexylammonium salt is a specialized compound widely utilized in biochemical research, particularly in the study of glucuronidation processes. This compound serves as a substrate for β-glucuronidase, making it an essential tool for researchers investigating drug metabolism and detoxification pathways. Its unique structure, featuring a brominated indole moiety, enhances its reactivity and specificity, allowing for precise applications in enzyme assays and metabolic studies.

In addition to its role in enzymatic studies, this compound has potential applications in the development of therapeutic agents, particularly in cancer research, where understanding glucuronidation can inform drug design and efficacy. The cyclohexylammonium salt form enhances solubility, making it easier to work with in various laboratory settings. Researchers can leverage this compound's unique properties to gain insights into metabolic processes, paving the way for advancements in pharmacology and toxicology.

Synonyms
Sel de glucuronide bleu·CHA
CAS Number
199326-16-4
Molecular Formula
C14H14BrNO7 · C6H13N
Molecular Weight
487.34
MDL Number
MFCD00214410
PubChem ID
53442180
Conditions
Conserver à 0-8°C
General Information
Synonyms
Sel de glucuronide bleu·CHA
CAS Number
199326-16-4
Molecular Formula
C14H14BrNO7 · C6H13N
Molecular Weight
487.34
MDL Number
MFCD00214410
PubChem ID
53442180
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

5-Bromo-3-indolyl b-D-glucuronide cyclohexylammonium salt is widely utilized in research focused on:

  • Biochemical Assays: This compound is often used as a substrate in enzyme assays, particularly for detecting β-glucuronidase activity, which is important in various biological and clinical studies.
  • Drug Metabolism Studies: Researchers employ this chemical to investigate the metabolism of drugs in the liver, helping to understand how medications are processed and their potential interactions.
  • Cellular Imaging: It serves as a valuable tool in cellular imaging techniques, allowing scientists to visualize specific cellular processes and pathways, enhancing the understanding of cellular functions.
  • Pharmaceutical Development: The compound plays a role in the development of new pharmaceuticals, particularly in the design of drugs that target glucuronidation pathways, which are crucial for drug efficacy and safety.
  • Environmental Monitoring: It is also applied in environmental science to study the biodegradation of pollutants, providing insights into the effectiveness of bioremediation strategies.

Citations