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  2. Tetrahydrocannabinol - Wikipedia

    en.wikipedia.org/wiki/Tetrahydrocannabinol

    The main metabolite in urine is the ester of glucuronic acid and 11-OH-THC and free THC-COOH. In the feces, mainly 11-OH-THC was detected. [37] Estimates of the elimination half-life of THC are variable. [23] THC was reported to have a fast initial half-life of 6 minutes and a long terminal half-life of 22 hours in a population pharmacokinetic ...

  3. Tetrahydrocannabiorcol - Wikipedia

    en.wikipedia.org/wiki/Tetrahydrocannabiorcol

    Δ 9-Tetrahydrocannabiorcol (Δ 9-THCC, (C1)-Δ 9-THC) is a phytocannabinoid found in Cannabis pollen. [1] It is a homologue of THC and THCV with the alkyl side chain replaced by a smaller methyl group.

  4. Delta-9-THC - Wikipedia

    en.wikipedia.org/?title=Delta-9-THC&redirect=no

    From or to a drug trade name: This is a redirect from (or to) the trade name of a drug to (or from) the international nonproprietary name (INN).

  5. Tetrahydrocannabutol - Wikipedia

    en.wikipedia.org/wiki/Tetrahydrocannabutol

    Δ 9-Tetrahydrocannabutol (tetrahydrocannabinol-C4, THC-C4, Δ 9-THCB, (C4)-Δ 9-THC, butyl-THC) is a phytocannabinoid found in cannabis that is a homologue of tetrahydrocannabinol (THC), the main active component of Cannabis. [1] Structurally, they are only different by the pentyl side chain being replaced by a butyl side chain.

  6. Tetrahydrocannabihexol - Wikipedia

    en.wikipedia.org/wiki/Tetrahydrocannabihexol

    Tetrahydrocannabihexol (Δ 9-THCH, Δ 9-Parahexyl, n-Hexyl-Δ 9-THC) is a phytocannabinoid, the hexyl homologue of tetrahydrocannabinol (THC) which was first isolated from Cannabis plant material in 2020 along with the corresponding hexyl homologue of cannabidiol, [1] [2] though it had been known for several decades prior to this as an isomer of the synthetic cannabinoid parahexyl. [3]

  7. Dimethylheptylpyran - Wikipedia

    en.wikipedia.org/wiki/Dimethylheptylpyran

    The original cannabinoid distillate (the precursor to EA-2233, called EA-1476 or "Red oil"), known today as delta-9-THC, was first created in 1949, and laboratory study of EA-1476 occurred in the mid-1950s. A single batch of EA-2233 was prepared by chemist Harry Pars of A.D. Little Labs in 1962 under a top-secret government contract.

  8. 8,11-Dihydroxytetrahydrocannabinol - Wikipedia

    en.wikipedia.org/wiki/8,11-Dihydroxytetrahydro...

    The 8β enantiomer retains psychoactive effects in animal studies with only slightly lower potency than THC, while the 8α enantiomer is much weaker. Both enantiomers have a shorter half-life in the body than 11-hydroxy-THC , making 8,11-dihydroxy-THC potentially useful for drug testing to distinguish between recent cannabis use and use longer ...

  9. Correct misinterpretations of free images. One of the main complaints about free images is lack of quality when compared with a promotional images. That is not true: there are very good free images as shown by Wikipedia:Featured pictures. In the case of replaceable images, it is possible that a promotional image will look better than free versions.