Saturated Cannabinoids: Update on Synthesis Strategies and Biological Studies of These Emerging Cannabinoid Analogs.
Maite L Docampo-Palacios, Giovanni A. Ramirez, Tesfay T Tesfatsion, Alex Okhovat, Monica Pittiglio, Kyle P Ray, Westley Cruces
Molecules September 4, 2023 DOI: 10.3390/molecules28176434 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Review Peer reviewed |
|---|---|
| Keywords | Cb1 receptor Cb2 receptor Gpcr Cannabilactones Cannabinoids Hexahydrocannabinol Hydrogenation Quinones |
| Key findings | The review reports that in vitro laboratory studies and studies in several animal species indicate HHC has broadly similar effects to Δ9-tetrahydrocannabinol, but HHC treatment has not been studied in humans, so its biological profile remains unestablished. |
Abstract
Natural and non-natural hexahydrocannabinols (HHC) were first described in 1940 by Adam and in late 2021 arose on the drug market in the United States and in some European countries. A background on the discovery, synthesis, and pharmacology studies of hydrogenated and saturated cannabinoids is described. This is harmonized with a summary and comparison of the cannabinoid receptor affinities of various classical, hybrid, and non-classical saturated cannabinoids. A discussion of structure-activity relationships with the four different pharmacophores found in the cannabinoid scaffold is added to this review. According to laboratory studies in vitro, and in several animal species in vivo, HHC is reported to have broadly similar effects to Δ9-tetrahydrocannabinol (Δ9-THC), the main psychoactive substance in cannabis, as demonstrated both in vitro and in several animal species in vivo. However, the effects of HHC treatment have not been studied in humans, and thus a biological profile has not been established.
Citations in the library
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