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Catalog Number:
29453
CAS Number:
93703-24-3
8-Bromo-3-methylxanthine
Purity:
≥ 99% (HPLC)
Documents
$18.53 /1G
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Product Information

8-Bromo-3-methylxanthine is a valuable compound in the field of biochemical research, particularly known for its role as a selective inhibitor of phosphodiesterases (PDEs). This compound exhibits unique properties that make it a crucial tool for studying cellular signaling pathways and the modulation of cyclic nucleotide levels. Its ability to selectively inhibit PDEs allows researchers to explore the therapeutic potential of manipulating these pathways in various conditions, including cardiovascular diseases and neurological disorders.

In addition to its research applications, 8-Bromo-3-methylxanthine is also utilized in the development of pharmaceuticals aimed at enhancing cognitive function and treating conditions such as asthma and chronic obstructive pulmonary disease (COPD). Its structural similarity to caffeine and other xanthines provides insights into the design of new drugs with improved efficacy and reduced side effects. With its specific action and versatility, 8-Bromo-3-methylxanthine stands out as a compound of interest for both academic and industrial researchers seeking innovative solutions in drug development.

CAS Number
93703-24-3
Purity
≥ 99% (HPLC)
Molecular Formula
C6H5BrN4O2
Molecular Weight
245.04
MDL Number
MFCD00462528
PubChem ID
1548797
Appearance
Light yellow to off-white powder
Conditions
Store at 0 - 8 °C
General Information
CAS Number
93703-24-3
Purity
≥ 99% (HPLC)
Molecular Formula
C6H5BrN4O2
Molecular Weight
245.04
MDL Number
MFCD00462528
PubChem ID
1548797
Appearance
Light yellow to off-white powder
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

8-Bromo-3-methylxanthine is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a valuable tool in the development of new drugs, particularly those targeting the central nervous system and respiratory diseases, due to its ability to modulate adenosine receptors.
  • Biochemical Research: It is commonly used in studies investigating the role of xanthine derivatives in cellular signaling pathways, helping researchers understand various physiological processes.
  • Anti-inflammatory Applications: The compound has shown potential in research aimed at developing anti-inflammatory agents, making it relevant for industries focused on chronic inflammatory conditions.
  • Neuroscience Studies: 8-Bromo-3-methylxanthine is employed in neuroscience to explore its effects on neurotransmitter release, which can lead to advancements in treatments for neurological disorders.
  • Comparative Studies: Its unique properties allow researchers to compare its effects with other xanthine derivatives, providing insights into structure-activity relationships that can guide the design of more effective compounds.

Citations