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Catalog Number:
21385
CAS Number:
125328-84-9
5-Bromo-4-chloro-3-indoxyl-β-L-fucopyranoside
Synonym(s):
5-Bromo-4-chloro-3-indolyl-β-L-fucopyranoside
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Product Information

5-Bromo-4-chloro-3-indoxyl-β-L-fucopyranoside is a versatile compound widely utilized in biochemical research and applications. This synthetic glycoside serves as a chromogenic substrate for the detection of β-galactosidase and other glycosidases, making it an essential tool in molecular biology and enzymology. Its unique structure allows for the visualization of enzymatic activity, facilitating studies in gene expression and metabolic pathways. Researchers appreciate its stability and specificity, which enhance the reliability of experimental results.

In addition to its role in enzyme assays, 5-Bromo-4-chloro-3-indoxyl-β-L-fucopyranoside is also employed in histochemical staining, providing clear and distinct coloration in tissue samples. This property is particularly valuable in histopathology and diagnostic applications, where accurate identification of cellular components is crucial. With its broad range of applications, this compound stands out for its effectiveness in both academic research and clinical settings, offering significant advantages over similar substrates in terms of sensitivity and ease of use.

Synonyms
5-Bromo-4-chloro-3-indolyl-β-L-fucopyranoside
CAS Number
125328-84-9
Molecular Formula
C14H15BrClNO5
Molecular Weight
392.63
MDL Number
MFCD00063688
PubChem ID
4520056
Conditions
Conserver à 0-8°C
General Information
Synonyms
5-Bromo-4-chloro-3-indolyl-β-L-fucopyranoside
CAS Number
125328-84-9
Molecular Formula
C14H15BrClNO5
Molecular Weight
392.63
MDL Number
MFCD00063688
PubChem ID
4520056
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-4-chloro-3-indoxyl-b-L-fucopyranoside is widely utilized in research focused on:

  • Enzyme Substrate Studies: This compound serves as a substrate for various enzymes, allowing researchers to study enzyme kinetics and mechanisms in biochemical pathways.
  • Histochemical Staining: It is used in histochemistry to visualize specific enzymes in tissue samples, providing insights into cellular functions and disease states.
  • Biochemical Assays: The compound is employed in assays to detect the presence of specific glycosidases, aiding in the identification of enzyme activity in different biological samples.
  • Plant Research: In plant biology, it helps in studying glycosylation processes, which are crucial for understanding plant development and responses to environmental stress.
  • Pharmaceutical Development: It plays a role in drug formulation studies, particularly in understanding how glycosylated compounds interact with biological systems, which is vital for developing effective therapeutics.

Citations