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  2. 11-Hydroxy-THC - Wikipedia

    en.wikipedia.org/wiki/11-Hydroxy-THC

    Like Δ 9-THC, 11-hydroxy-THC is a partial agonist at the cannabinoid receptor CB 1, but with significantly higher binding affinity (K i = 0.37 nM compared to Δ 9-THC K i = 35 nM). [7] With respect to cAMP inhibition at CB 1 it displays a similar efficacy to that of Δ 9 -THC (EC 50 = 11 nM vs. EC 50 = 5.2 nM, respectively), but a lower ...

  3. 11-Hydroxy-Δ-8-THC - Wikipedia

    en.wikipedia.org/wiki/11-Hydroxy-Δ-8-THC

    11-Hydroxy-Δ-8-tetrahydrocannabinol (11-OH-Δ 8-THC, alternatively numbered as 7-OH-Δ 6-THC) is an active metabolite of Δ 8-THC, a psychoactive cannabinoid found in small amounts in cannabis. It is an isomer of 11-OH-Δ 9-THC, and is produced via the same metabolic pathway. It was the first cannabinoid metabolite discovered in 1970.

  4. Tetrahydrocannabinol - Wikipedia

    en.wikipedia.org/wiki/Tetrahydrocannabinol

    The principal active metabolite of THC is 11-hydroxy-THC (11-OH-THC), which is formed by CYP2C9 and is psychoactive similarly to THC. [31] [22] [21] This metabolite is further oxidized to 11-nor-9-carboxy-THC (THC-COOH). In animals, more than 100 metabolites of THC could be identified, but 11-OH-THC and THC-COOH are the predominant metabolites ...

  5. 11-Hydroxycannabinol - Wikipedia

    en.wikipedia.org/wiki/11-Hydroxycannabinol

    11-Hydroxycannabinol (11-OH-CBN) is the main active metabolite of cannabinol (CBN), one of the active components of cannabis, [1] and has also been isolated from cannabis itself. [2] It is more potent than CBN itself, acting as an agonist of CB 1 with around the same potency as THC , but is a weak antagonist at CB 2 .

  6. How Long Do Edibles Last? The Duration and Effects of ... - AOL

    www.aol.com/long-edibles-last-duration-effects...

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  7. Δ-11-Tetrahydrocannabinol - Wikipedia

    en.wikipedia.org/wiki/Δ-11-Tetrahydrocannabinol

    Δ-11-Tetrahydrocannabinol (Delta-11-THC, Δ 11-THC, Δ 9(11)-THC, exo-Tetrahydrocannabinol) is a rare isomer of tetrahydrocannabinol, developed in the 1970s. It can be synthesised from Δ 8 -THC by several different routes, [ 1 ] [ 2 ] [ 3 ] though only the (6aR, 10aR) enantiomer is known.

  8. Marijuana use linked to depression, bipolar disorder and ...

    www.aol.com/news/theres-growing-evidence...

    D’Souza added that cannabis use can have serious impacts on the developing brain because of its effects on the endocannabinoid system, a complex signaling system in the brain that marijuana targets.

  9. Cannabinoid - Wikipedia

    en.wikipedia.org/wiki/Cannabinoid

    In Phase III trials, the most common adverse effects were dizziness, drowsiness and disorientation; 12% of subjects stopped taking the drug because of the side effects. [ 57 ] Dronabinol (brand names Marinol and Syndros) is a delta-9-THC containing drug for treating HIV/AIDS -induced anorexia and chemotherapy-induced nausea and vomiting .