JZL184

10mM in DMSO

  • Product Code: 201291
  CAS:    1101854-58-3
Molecular Weight: 520.49 g./mol Molecular Formula: C₂₇H₂₄N₂O₉
EC Number: MDL Number: MFCD12912421
Melting Point: Boiling Point:
Density: Storage Condition: -20°C
Product Description: JZL184 is primarily used in scientific research to study the endocannabinoid system, specifically as a selective inhibitor of the enzyme monoacylglycerol lipase (MAGL). By inhibiting MAGL, JZL184 increases levels of 2-arachidonoylglycerol (2-AG), a major endocannabinoid, in the brain and peripheral tissues. This action allows researchers to investigate the role of 2-AG in processes such as pain modulation, inflammation, anxiety, and neurodegeneration. It has been applied in preclinical models to explore potential therapeutic strategies for conditions like chronic pain, multiple sclerosis, and neuroinflammatory diseases. Due to its ability to modulate cannabinoid receptor signaling indirectly, JZL184 helps differentiate the effects of elevated endocannabinoids from those of direct cannabinoid receptor agonists. It is not used clinically and remains a tool compound for pharmacological and neurochemical studies.
Sizes / Availability / Pricing:
Size Availability Price Quantity
1ml 10-20 days ฿2,660.00
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JZL184
JZL184 is primarily used in scientific research to study the endocannabinoid system, specifically as a selective inhibitor of the enzyme monoacylglycerol lipase (MAGL). By inhibiting MAGL, JZL184 increases levels of 2-arachidonoylglycerol (2-AG), a major endocannabinoid, in the brain and peripheral tissues. This action allows researchers to investigate the role of 2-AG in processes such as pain modulation, inflammation, anxiety, and neurodegeneration. It has been applied in preclinical models to explore potential therapeutic strategies for conditions like chronic pain, multiple sclerosis, and neuroinflammatory diseases. Due to its ability to modulate cannabinoid receptor signaling indirectly, JZL184 helps differentiate the effects of elevated endocannabinoids from those of direct cannabinoid receptor agonists. It is not used clinically and remains a tool compound for pharmacological and neurochemical studies.
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