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Catalog Number:
00441
CAS Number:
114162-64-0
Sel de cyclohexylammonium de 5-bromo-4-chloro-3-indolyl-β-D-glucuronide
Purity:
≥ 99 % (CCM)
Synonym(s):
X-Glc·CHA, X-GlcA, sel de X-glucuronide CHA
Documents
$30.20 /100 mg
Taille
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Informations sur le produit

5-Bromo-4-chloro-3-indolyl-β-D-glucuronide cyclohexylammonium salt is a versatile compound widely utilized in biochemical research, particularly in the study of enzyme activity and cellular processes. This compound serves as a substrate for β-glucuronidase, making it invaluable in assays that measure enzyme activity in various biological samples. Its unique structure allows for effective labeling and detection in histochemical applications, providing researchers with a reliable tool for visualizing enzyme localization within tissues.

Additionally, this compound is beneficial in drug metabolism studies, where it aids in understanding the conjugation processes of pharmaceuticals. Its stability and solubility in biological systems enhance its applicability in both in vitro and in vivo studies. Researchers appreciate its ease of use and the clarity it brings to experimental results, making it a preferred choice for those investigating metabolic pathways and enzyme kinetics.

Numéro CAS 
114162-64-0
Formule moléculaire
C14H13BrClNO7 · C6H13N
Poids moléculaire 
521.8
Rotation optique 
[a] D 20 = -90,8 ± 2,5º (C = 1 dans DMF:H 2 O (1:1))base
Informations générales
Numéro CAS 
114162-64-0
Formule moléculaire
C14H13BrClNO7 · C6H13N
Poids moléculaire 
521.8
Rotation optique 
[a] D 20 = -90,8 ± 2,5º (C = 1 dans DMF:H 2 O (1:1))base
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

5-Bromo-4-chloro-3-indolyl-b-D-glucuronide cyclohexylammonium salt is widely utilized in research focused on:

  • Biochemical Assays: This compound is used as a substrate in enzyme assays, particularly for measuring the activity of β-glucuronidase, which is important in drug metabolism studies.
  • Histochemical Staining: It serves as a chromogenic substrate for visualizing enzyme activity in tissue samples, aiding researchers in understanding cellular processes and disease mechanisms.
  • Drug Development: The compound plays a role in pharmacological research, helping scientists evaluate the efficacy and safety of new drugs by monitoring metabolic pathways.
  • Environmental Studies: It is applied in studies assessing the biodegradation of pharmaceuticals in wastewater, providing insights into environmental impacts and remediation strategies.
  • Genetic Research: The compound is utilized in the study of gene expression, allowing researchers to track the activity of specific genes in various biological contexts.

Citations