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| TABLE 2.2 Compounds That Bind to Cannabinoid Receptors |
| Compound | Properties | ||
| Agonists (receptor activators) | |||
| Plant-derived compounds | |||
| Main psychoactive cannabinoid in marijuana plant; largely responsible for psychological and physiological effects (except in discussions of the different forms of THC, THC is used as a synonym for |
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| Slightly less potent than |
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| 11-OH- |
Bioactive compound formed when body breaks down |
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| Cannabinoid agonists found in animals | |||
| Anandamide (arachidonyl-ethanolamide) | Found in animals ranging from mollusks to mammals; appears to be primary endogenous cannabinoid agonist in mammals; chemical structure very different from plant cannabinoids and related to prostaglandins. | ||
| 2-AG (arachidonyl glycerol) | Endogenous agonist; structurally similar to anandamide; more abundant but less potent than anandamide. | ||
| THC analogues | |||
| Dronabinol | Synthetic THC; marketed in the United States as Marinol for nausea associated with chemotherapy and for AIDS-related wasting. | ||
| Nabilone | THC analogue; marketed in the United Kingdom as Cesamet for same indications as dronabionol. | ||
| CP 55,940 | Synthetic cannabinoid; THC analogue; that is, it is structurally similar to THC. | ||
| Levonantradol | THC analogue. | ||
| HU-210 | THC analogue, 100- to 800-fold greater potency than THC97. | ||
| Chemical structure unlike THC or anandamide | |||
| WIN-55,212-2 | Chemical structure different from known cannabinoids, but binds to both cannabinoid receptors; chemically related to cyclo-oxygenase inhibitors, which include antiinflammatory drugs. | ||
| Antagonists (receptor blockers) | |||
| SR 141716A | Synthetic CB1 antagonist; developed in 1994132. | ||
| SR 144528 | Synthetic CB2 antagonist; developed in 1997133. | ||
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