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Catalog Number:
10644
CAS Number:
97753-82-7
5-Bromoindol-3-yl-β-D-galactoside
Purity:
≥ 99 % (HPLC)
Synonym(s):
5-Bromo-3-indolyl-β-D-galactopyranoside, 5-Bromo-3-indoxyl-β-D-galactopyranoside
Documents
$25.20 /250 mg
Taille
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Product Information

Substrat de la bêta-galactosidase qui est transformé, par l'enzyme, en un chromophore bleu insoluble. Il est également utilisé dans les systèmes de détection du gène Lac, dans les immunoblots et les tests immunohistochimiques.

Synonyms
5-Bromo-3-indolyl-β-D-galactopyranoside, 5-Bromo-3-indoxyl-β-D-galactopyranoside
CAS Number
97753-82-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C14H16BrNO6
Molecular Weight
374.19
MDL Number
MFCD00063691
PubChem ID
4373342
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 20 = -34 ± 2 º (C = 1 dans DMF:H2O 1:1)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
5-Bromo-3-indolyl-β-D-galactopyranoside, 5-Bromo-3-indoxyl-β-D-galactopyranoside
CAS Number
97753-82-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C14H16BrNO6
Molecular Weight
374.19
MDL Number
MFCD00063691
PubChem ID
4373342
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 20 = -34 ± 2 º (C = 1 dans DMF:H2O 1:1)
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-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.

Citations