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The aromatic terpenoids begin to vaporize at 126.0 °C (258.8 °F), but the more bioactive tetrahydrocannabinol (THC), and other cannabinoids also found in cannabis (often legally sold as cannabinoid isolates) like cannabidiol (CBD), cannabichromene (CBC), cannabigerol (CBG), cannabinol (CBN), do not vaporize until near their respective boiling ...
Monoterpenes myrcene and sesquiterpenes β-caryophyllene (binds to the human CB2 cannabinoids receptor) and α-humulene are the most common terpene compounds, and are present in most varieties of cannabis strains. The lack of exact standards makes it sometimes difficult for scientists to classify new terpenes.
Tea (Camellia sinensis) catechins have an affinity for human cannabinoid receptors. [43] A widespread dietary terpene, beta-caryophyllene, a component from the essential oil of cannabis and other medicinal plants, has also been identified as a selective agonist of peripheral CB 2-receptors, in vivo. [44] Black truffles contain anandamide. [45]
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A dried cannabis flower. The short-term effects of cannabis are caused by many chemical compounds in the cannabis plant, including 113 [clarification needed] different cannabinoids, such as tetrahydrocannabinol, and 120 terpenes, [1] which allow its drug to have various psychological and physiological effects on the human body.
Female cannabis plants contain at least 113 cannabinoids, [55] including cannabidiol (CBD), thought to be the major anticonvulsant that helps people with multiple sclerosis, [56] and cannabichromene (CBC), an anti-inflammatory which may contribute to the pain-killing effect of cannabis.
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The terpene alpha-pinene is a major component of the common solvent, turpentine. The one terpene that has major applications is natural rubber (i.e., polyisoprene). The possibility that other terpenes could be used as precursors to produce synthetic polymers has been investigated. Many terpenes have been shown to have pharmacological effects.
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