Abeo-HHC acetate

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Synthetic cannabinoid


Abeo-HHC acetate
INN
Drug class
Routes of administration
Pregnancy category
Bioavailability
Metabolism
Elimination half-life
Excretion
Legal status
CAS Number 71902-08-4
PubChem 3080631
DrugBank
ChemSpider 2338855
KEGG


Abeo-HHC acetate is a synthetic cannabinoid derivative that is structurally related to hexahydrocannabinol (HHC). It is a chemical compound that has been studied for its potential effects on the endocannabinoid system.

Chemical Structure[edit | edit source]

Chemical structure of Abeo-HHC acetate

Abeo-HHC acetate is characterized by its unique chemical structure, which includes a hexahydrobenzo[c]chromene core. The compound is an acetate ester of abeo-hexahydrocannabinol, which means it has an acetyl group attached to the hydroxyl group of the cannabinoid.

Pharmacology[edit | edit source]

Abeo-HHC acetate interacts with the cannabinoid receptors in the central nervous system. These receptors, primarily CB1 and CB2, are part of the endocannabinoid system, which plays a role in regulating various physiological processes such as mood, appetite, and pain sensation.

Synthesis[edit | edit source]

The synthesis of Abeo-HHC acetate involves the chemical modification of hexahydrocannabinol. The process typically includes the acetylation of the hydroxyl group, resulting in the formation of the acetate ester. This modification can alter the pharmacokinetic properties of the compound, potentially affecting its potency and duration of action.

Potential Applications[edit | edit source]

Research into Abeo-HHC acetate is ongoing, with studies exploring its potential therapeutic applications. Like other cannabinoids, it may have potential uses in the treatment of conditions such as chronic pain, inflammation, and neurological disorders. However, more research is needed to fully understand its effects and safety profile.

Legal Status[edit | edit source]

The legal status of Abeo-HHC acetate varies by jurisdiction. In some regions, it may be classified as a controlled substance due to its structural similarity to other cannabinoids. Researchers and manufacturers must comply with local regulations when working with this compound.

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Contributors: Prab R. Tumpati, MD