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Catalog Number:
21381
CAS Number:
133950-70-6
Nonanoate de 5-bromo-3-indoxyle
Synonym(s):
Nonanoate de 5-bromo-3-indolyle
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Product Information

5-Bromo-3-indoxyl nonanoate is a versatile compound recognized for its significant role in biochemical research and applications. This compound serves as a substrate for various enzymatic reactions, particularly in the study of β-glucuronidase and other glycosidases, making it invaluable in the field of molecular biology. Its unique structure allows for the visualization of enzyme activity, which is crucial for researchers aiming to understand metabolic pathways and enzyme kinetics.

In addition to its research applications, 5-Bromo-3-indoxyl nonanoate is utilized in the development of diagnostic assays and biosensors, where its ability to produce a colorimetric response upon enzymatic cleavage can be harnessed for sensitive detection methods. This compound stands out due to its stability and ease of use, providing researchers with a reliable tool for various experimental setups. Its potential extends to applications in drug discovery and environmental monitoring, where it can aid in the detection of specific enzymes related to disease states or environmental pollutants.

Synonyms
Nonanoate de 5-bromo-3-indolyle
CAS Number
133950-70-6
Molecular Formula
C 17 H 22 BrNO 2
Molecular Weight
352.27
MDL Number
MFCD02683905
PubChem ID
10154980
Conditions
Conserver à 0-8°C
General Information
Synonyms
Nonanoate de 5-bromo-3-indolyle
CAS Number
133950-70-6
Molecular Formula
C 17 H 22 BrNO 2
Molecular Weight
352.27
MDL Number
MFCD02683905
PubChem ID
10154980
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-indoxyl nonanoate 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.
  • Histochemical Staining: It is employed in histochemistry for visualizing specific cellular components, aiding in the identification of tissue types and disease states.
  • Drug Development: The compound is used in the pharmaceutical industry to develop new drugs, particularly those targeting specific biological pathways involving indole derivatives.
  • Environmental Monitoring: It can be utilized in environmental science to assess the presence of certain pollutants, contributing to ecological studies and assessments.
  • Educational Purposes: This chemical is often included in laboratory courses for students studying organic chemistry and biochemistry, providing hands-on experience with indole derivatives.

Citations