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Catalog Number:
10644
CAS Number:
97753-82-7
5-bromoindol-3-il-β-D-galactósido
Purity:
≥ 99 % (HPLC)
Synonym(s):
5-Bromo-3-indolil-β-D-galactopiranósido, 5-Bromo-3-indoxil-β-D-galactopiranósido
Documents
$25.20 /250 mg
Tamaño
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Product Information

Sustrato para la beta-galactosidasa que es convertido, por la enzima, en un cromóforo azul índigo insoluble. También se utiliza en sistemas de detección del gen Lac, en ensayos de inmunotransferencia e inmunocitoquímica.

Synonyms
5-Bromo-3-indolil-β-D-galactopiranósido, 5-Bromo-3-indoxil-β-D-galactopiranósido
CAS Number
97753-82-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C14H16BrNO6
Molecular Weight
374.19
MDL Number
MFCD00063691
PubChem ID
4373342
Appearance
Polvo de color blanco a blanquecino
Optical Rotation
[a] D 20 = -34 ± 2 º (C=1 en DMF:H2O 1:1)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
5-Bromo-3-indolil-β-D-galactopiranósido, 5-Bromo-3-indoxil-β-D-galactopiranósido
CAS Number
97753-82-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C14H16BrNO6
Molecular Weight
374.19
MDL Number
MFCD00063691
PubChem ID
4373342
Appearance
Polvo de color blanco a blanquecino
Optical Rotation
[a] D 20 = -34 ± 2 º (C=1 en DMF:H2O 1:1)
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

5-Bromoindol-3-yl-b-D-galactoside is widely utilized in research focused on:

  • Biochemical Research: This compound serves as a substrate in enzyme assays, particularly for studying glycosylation processes, which are crucial in understanding various biological functions.
  • Drug Development: Its unique structure allows researchers to explore its potential as a lead compound in developing new pharmaceuticals, especially in targeting specific biological pathways.
  • Cell Biology: Used in cell culture studies, it helps in investigating cell signaling pathways and the effects of glycosylation on cell behavior, providing insights into cancer research.
  • Neuroscience: The compound's bromine atom can be beneficial in tracing studies, helping scientists understand neurotransmitter interactions and their implications in neurological disorders.
  • Natural Product Synthesis: It can be employed in the synthesis of complex natural products, aiding chemists in creating compounds with potential therapeutic effects.

Citas