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Cannabichromene is a non-psychoactive phytocannabinoid found in the Cannabis plant. It is one of the most abundant cannabinoids after THC and CBD. Cannabichromene acts primarily as a selective agonist at the Cannabinoid receptor type 2 (CB2) and has low affinity for CB1 receptors. It also activates Transient receptor potential ankyrin 1 channel (TRPA1) and Transient receptor potential vanilloid 1 channel (TRPV1), which are involved in pain perception and inflammation. Preclinical studies suggest that CBC exhibits modest antinociceptive (pain-reducing), anti-inflammatory effects, neuroprotective properties, anticonvulsant activity in animal models, and may inhibit cancer cell growth in vitro. Its mechanism includes modulation of endocannabinoid tone by inhibiting cellular reuptake of endocannabinoids and weak inhibition of monoacylglycerol lipase (MAGL). There are currently no FDA-approved medications based on CBC[1][3][4][5][6][7].
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