CB1/2 Agonist 1 is a selective cannabinoid receptor agonist, targeting both CB1 and CB2 receptors with EC50 values of 56.15 nM and 11.63 nM, respectively. This compound effectively reduces glutamate release and LPS-induced microglial cell activation, demonstrating significant anti-inflammatory and antinociceptive properties. Due to its unique pharmacological profile, CB1/2 Agonist 1 has potential applications in research related to multiple sclerosis and other neuroinflammatory conditions.
CB1/2 Agonist 1 is a selective cannabinoid receptor agonist, targeting both CB1 and CB2 receptors with EC50 values of 56.15 nM and 11.63 nM, respectively. This compound effectively reduces glutamate release and LPS-induced microglial cell activation, demonstrating significant anti-inflammatory and antinociceptive properties. Due to its unique pharmacological profile, CB1/2 Agonist 1 has potential applications in research related to multiple sclerosis and other neuroinflammatory conditions.
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