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  2. Conversion of CBD to THC - Wikipedia

    en.wikipedia.org/wiki/Conversion_of_CBD_to_THC

    By heat. CBD heated to 175, [13] or 250–300 °C may partially be converted into THC. [14] Even at room temperature, trace amounts of THC can be formed as a contaminant in CBD stored for long periods in the presence of moisture and carbon dioxide in the air, with storage under inert gas required to maintain analytically pure CBD.

  3. Cannabinol - Wikipedia

    en.wikipedia.org/wiki/Cannabinol

    Cannabinol (CBN) is a mildly psychoactive cannabinoid (e.g., cannabidiol (CBD)) that acts as a low affinity partial agonist at both CB 1 and CB 2 receptors. This activity at CB 1 and CB 2 receptors constitutes interaction of CBN with the endocannabinoid system (ECS). Although CBN shares the same mechanism of action as other phytocannabinoids (e ...

  4. Tetrahydrocannabinolic acid - Wikipedia

    en.wikipedia.org/wiki/Tetrahydrocannabinolic_acid

    Tetrahydrocannabinolic acid (THCA, 2-COOH-THC; conjugate base tetrahydrocannabinolate) is a precursor of tetrahydrocannabinol (THC), an active component of cannabis. [1]THCA is found in variable quantities in fresh, undried cannabis, but is progressively decarboxylated to THC with drying, and especially under intense heating such as when cannabis is smoked or cooked into cannabis edibles.

  5. Cannabidiol - Wikipedia

    en.wikipedia.org/wiki/Cannabidiol

    Cannabidiol, in an oral-mucosal spray formulation combined with delta-9-tetrahydrocannabinol, is a product available by prescription for the relief of severe spasticity due to multiple sclerosis (where other anti- spasmodics have not been effective) in the United Kingdom. [141]

  6. Cannabinoid - Wikipedia

    en.wikipedia.org/wiki/Cannabinoid

    CBN was the first cannabis compound to be isolated from cannabis extract in the late 1800s. Its structure and chemical synthesis were achieved by 1940 [ 34 ] , followed by some of the first pre-clinical research studies to determine the effects of individual cannabis-derived compounds in vivo . [ 35 ]

  7. Tetrahydrocannabivarin - Wikipedia

    en.wikipedia.org/wiki/Tetrahydrocannabivarin

    Tetrahydrocannabivarin. Tetrahydrocannabivarin (THCV, THV, O-4394, GWP42004) is a homologue of tetrahydrocannabinol (THC) having a propyl (3-carbon) side chain instead of pentyl (5-carbon), making it non- psychoactive in lower doses. It has been shown to exhibit neuroprotective activity, appetite suppression, glycemic control and reduced side ...

  8. Synthetic cannabinoids - Wikipedia

    en.wikipedia.org/wiki/Synthetic_cannabinoids

    Synthetic cannabinoids reagent testing kits have recently become economical. It is often difficult to determine what is in these products without reagent testing because masking agents, such as tocopherol (or vitamin E acetate that causes vaping-associated pulmonary injury), eugenol, and fatty acids, are added to confound identification.

  9. Δ-8-Tetrahydrocannabinol - Wikipedia

    en.wikipedia.org/wiki/Δ-8-Tetrahydrocannabinol

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Δ-8-tetrahydrocannabinol (delta-8-THC, [ a ]Δ8-THC) is a psychoactive cannabinoid found in the Cannabis plant. [ 1 ] It is an isomer of delta-9-tetrahydrocannabinol (delta-9-THC, Δ 9 -THC), the compound commonly known as THC ...