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On July 12, 2016, 33 people were intoxicated by an herbal "incense" product called "AK-47 24 Karat Gold", [105] and dozens overdosed, in Brooklyn. Eighteen people were transported to local hospitals. [106] The herbal "incense" product was determined to be a synthetic cannabinoid called AMB-FUBINACA. [105]
On the 19th of January 2009, the University of Freiburg in Germany announced that an analog of CP 47,497 is the main active ingredient in the herbal "incense" product Spice, specifically the 1,1-dimethyloctyl homologue of CP 47,497. Both the dimethylheptyl and dimethyloctyl homologues were detected in different batches, with considerable ...
Cannabicyclohexanol (CCH, CP 47,497 dimethyloctyl homologue, (C8)-CP 47,497) is a cannabinoid receptor agonist drug, developed by Pfizer in 1979. On 19 January 2009, the University of Freiburg in Germany announced that an analog of CP 47,497 was the main active ingredient in the herbal incense product Spice, specifically the 1,1-dimethyloctyl homologue of CP 47,497, which is now known as ...
This Cannabis -related article is a stub. You can help Wikipedia by expanding it.
JWH-018 is a full agonist of both the CB 1 and CB 2 cannabinoid receptors, with a reported binding affinity of 9.00 ± 5.00 nM at CB 1 and 2.94 ± 2.65 nM at CB 2. [6] JWH-018 has an EC 50 of 102 nM for human CB 1 receptors, and 133 nM for human CB 2 receptors. [16]
The smoke of the inner bark of the tree is used by shamans of the indigenous people of Venezuela in cases of fever conditions, or cooked for driving out evil ghosts. [31] Salvia: Salvia divinorum: Leaf: Salvinorin A and other salvinorins: Psychedelic: Mazatec [32] San Pedro cactus: Trichocereus macrogonus var. pachanoi (syn. Echinopsis pachanoi ...
Jennifer Grey looked back on how a sex scene with Patrick Swayze — that was ultimately cut from 1984’s Red Dawn — was derailed by him being drunk, and her "smoking a lot of weed" at the time.
QMPSB is an arylsulfonamide-based synthetic cannabinoid that has been sold as a designer drug. [1]QMPSB was first discovered by Nathalie Lambeng and colleagues in 2007. It acts as a full agonist of the CB 1 receptor and CB 2 receptor with K i values of 3 nM and 4 nM, respectively. [2]
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