DescriptionHigh affinity and selective CB1 antagonist (Ki = 3.3 nM). Exhibits >100-fold selectivity for CB1 over CB2 receptors. Improves glucose homeostasis, reverses hepatic steatosis and reduces body weight in diet-induced obese mice. Orally available and non-brain penetrant.
|Bioactive Small Molecule|
Safety and Handling
Recommended Storage : Store at 4°C
Research Use Only. Not For Human or Veterinary Use
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