Cannabicyclohexanol: Difference between revisions

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'''Cannabicyclohexanol''' (also known as '''CP 47,497-C8''' or '''CP 47,497''' homologue) is a synthetic cannabinoid that mimics the effects of natural [[cannabinoids]] found in [[Cannabis (drug)|cannabis]]. It is one of the cannabinoids responsible for the psychoactive effects of cannabis.
== Cannabicyclohexanol ==


== History ==
[[File:Cannabicyclohexanol_isomers.png|thumb|right|300px|Structural isomers of Cannabicyclohexanol]]
Cannabicyclohexanol was first synthesized in the mid-1970s by the pharmaceutical company [[Pfizer]]. It was developed as part of a research program to find cannabinoid analogues that could be used for therapeutic purposes. However, it was never marketed as a drug and its potential medical uses remain largely unexplored.


== Chemistry ==
'''Cannabicyclohexanol''' is a synthetic cannabinoid that has been used in the formulation of synthetic cannabis products. It is known for its potent psychoactive effects and has been a subject of interest in both medical and legal contexts.
Cannabicyclohexanol is a synthetic cannabinoid, which means it is a man-made chemical that is similar in structure to the natural cannabinoids found in cannabis. It is a homologue of CP 47,497, a compound that was also developed by Pfizer. The "C8" in its name refers to the eight-carbon chain that connects the two cyclohexanol rings in its structure.


== Effects ==
=== Chemical Structure ===
Like other synthetic cannabinoids, cannabicyclohexanol binds to the same receptors in the brain as THC, the main psychoactive compound in cannabis. This means it can produce similar effects, including feelings of euphoria, altered perception, and increased appetite. However, because it is a synthetic compound, its effects can be much stronger and more unpredictable than those of natural cannabinoids.
Cannabicyclohexanol, also known as CP-47,497-C8, is a derivative of the compound CP-47,497. It is characterized by the addition of a cyclohexyl group to the structure, which significantly increases its affinity for the [[cannabinoid receptor]]s in the brain. The chemical formula for Cannabicyclohexanol is C26H40O2.


== Legal status ==
=== Mechanism of Action ===
Cannabicyclohexanol is a controlled substance in many countries, including the United States, where it is classified as a Schedule I drug under the Controlled Substances Act. This means it is illegal to manufacture, distribute, or possess without a license.
Cannabicyclohexanol acts as a full agonist at the [[CB1 receptor]] and [[CB2 receptor]], which are part of the endocannabinoid system. This system is involved in regulating various physiological processes including mood, memory, and pain sensation. The binding of Cannabicyclohexanol to these receptors mimics the effects of [[tetrahydrocannabinol]] (THC), the active component of [[cannabis]].


== See also ==
=== Effects ===
* [[Cannabinoid]]
The effects of Cannabicyclohexanol are similar to those of THC but are often more intense due to its higher potency. Users may experience euphoria, altered perception, and relaxation. However, adverse effects such as anxiety, paranoia, and tachycardia have also been reported.
 
=== Legal Status ===
Due to its potent effects and potential for abuse, Cannabicyclohexanol has been classified as a controlled substance in many countries. It is often included in the list of substances banned under synthetic cannabinoid regulations.
 
=== Health Implications ===
The use of Cannabicyclohexanol has been associated with several health risks. Acute intoxication can lead to severe psychological and physiological effects, and chronic use may result in dependency and withdrawal symptoms. The lack of regulation in synthetic cannabis products also poses a risk of contamination and inconsistent dosing.
 
== Related Pages ==
* [[Synthetic cannabinoids]]
* [[Synthetic cannabinoids]]
* [[Cannabis (drug)]]
* [[Cannabinoid receptor]]
* [[Tetrahydrocannabinol]]
* [[Endocannabinoid system]]
 
{{Cannabinoids}}


[[Category:Synthetic cannabinoids]]
[[Category:Synthetic cannabinoids]]
[[Category:Pharmaceuticals]]
[[Category:Chemical compounds]]
[[Category:Drugs]]
<gallery>
 
File:Cannabicyclohexanol.svg|Cannabicyclohexanol
{{stub}}
File:Cannabicyclohexanol_isomers.png|Cannabicyclohexanol isomers
</gallery>

Latest revision as of 00:58, 18 February 2025

Cannabicyclohexanol[edit]

Structural isomers of Cannabicyclohexanol

Cannabicyclohexanol is a synthetic cannabinoid that has been used in the formulation of synthetic cannabis products. It is known for its potent psychoactive effects and has been a subject of interest in both medical and legal contexts.

Chemical Structure[edit]

Cannabicyclohexanol, also known as CP-47,497-C8, is a derivative of the compound CP-47,497. It is characterized by the addition of a cyclohexyl group to the structure, which significantly increases its affinity for the cannabinoid receptors in the brain. The chemical formula for Cannabicyclohexanol is C26H40O2.

Mechanism of Action[edit]

Cannabicyclohexanol acts as a full agonist at the CB1 receptor and CB2 receptor, which are part of the endocannabinoid system. This system is involved in regulating various physiological processes including mood, memory, and pain sensation. The binding of Cannabicyclohexanol to these receptors mimics the effects of tetrahydrocannabinol (THC), the active component of cannabis.

Effects[edit]

The effects of Cannabicyclohexanol are similar to those of THC but are often more intense due to its higher potency. Users may experience euphoria, altered perception, and relaxation. However, adverse effects such as anxiety, paranoia, and tachycardia have also been reported.

Legal Status[edit]

Due to its potent effects and potential for abuse, Cannabicyclohexanol has been classified as a controlled substance in many countries. It is often included in the list of substances banned under synthetic cannabinoid regulations.

Health Implications[edit]

The use of Cannabicyclohexanol has been associated with several health risks. Acute intoxication can lead to severe psychological and physiological effects, and chronic use may result in dependency and withdrawal symptoms. The lack of regulation in synthetic cannabis products also poses a risk of contamination and inconsistent dosing.

Related Pages[edit]