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Catalog Number:
21410
CAS Number:
156117-44-1
6-Cloro-3-indoxil- N -acetil-β-D-galactosaminida
Synonym(s):
6-Cloro-3-indoxil-2-acetamido-2-desoxi-β-D-galactopiranósido, 6-Cloro-3-(2-acetamido-2-desoxi-β-D-galactopiranosiloxi)indol
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Product Information

6-Chloro-3-indoxyl-N-acetyl-b-D-galactosaminide is a versatile compound widely utilized in biochemical research and diagnostics. This compound serves as a substrate for various enzymes, particularly in the study of glycosylation processes and enzyme activity assays. Its unique structure, featuring a chloroindole moiety, allows for specific interactions with enzymes, making it an invaluable tool for researchers investigating carbohydrate metabolism and related pathways.

In practical applications, this compound is often employed in histochemical staining techniques, enabling the visualization of glycosylated proteins in tissue samples. This capability is crucial for understanding disease mechanisms, particularly in cancer research, where altered glycosylation patterns can indicate tumor progression. Additionally, its use in enzyme-linked assays enhances the sensitivity and specificity of detection methods, providing researchers with reliable results. With its unique properties and broad applicability, 6-Chloro-3-indoxyl-N-acetyl-b-D-galactosaminide stands out as a key reagent for advancing research in biochemistry and molecular biology.

Synonyms
6-Cloro-3-indoxil-2-acetamido-2-desoxi-β-D-galactopiranósido, 6-Cloro-3-(2-acetamido-2-desoxi-β-D-galactopiranosiloxi)indol
CAS Number
156117-44-1
Molecular Formula
C16H19ClN2O6
Molecular Weight
370.79
MDL Number
MFCD02683907
PubChem ID
22345917
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
6-Cloro-3-indoxil-2-acetamido-2-desoxi-β-D-galactopiranósido, 6-Cloro-3-(2-acetamido-2-desoxi-β-D-galactopiranosiloxi)indol
CAS Number
156117-44-1
Molecular Formula
C16H19ClN2O6
Molecular Weight
370.79
MDL Number
MFCD02683907
PubChem ID
22345917
Conditions
Conservar entre 0 y 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-galactosaminide is widely utilized in research focused on:

  • Biochemical Assays: This compound serves as a substrate in enzyme assays, particularly for studying glycosyltransferases, which are crucial for understanding carbohydrate metabolism.
  • Fluorescent Labeling: It is used in the development of fluorescent probes for imaging applications, enhancing the visualization of cellular processes in biological research.
  • Drug Development: The compound plays a role in medicinal chemistry, aiding in the design of new drugs targeting specific enzymes or pathways related to diseases.
  • Diagnostic Tools: It is incorporated into diagnostic kits for detecting specific enzymes or biomarkers, providing valuable information for disease diagnosis and monitoring.
  • Research on Glycobiology: This chemical is essential in studies related to glycobiology, helping researchers understand the role of carbohydrates in cell signaling and interactions.

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