JWH-175
Overview
JWH-175 is a synthetic cannabinoid that acts as a potent agonist at the cannabinoid receptors. It is part of the naphthoylindole family of compounds, which are known for their psychoactive effects. JWH-175 was developed by Dr. John W. Huffman and his team at Clemson University as part of their research into the structure and function of cannabinoid receptors.
Chemical Structure
JWH-175 is characterized by its naphthoylindole structure, which includes a naphthalene ring linked to an indole group. The specific chemical formula for JWH-175 is C24H23NO, and it has a molecular weight of 341.45 g/mol. The compound is known for its high affinity for the CB1 and CB2 receptors, which are part of the endocannabinoid system.
Pharmacology
JWH-175 functions as a full agonist at both the CB1 and CB2 receptors. These receptors are part of the G protein-coupled receptor family and are primarily involved in the modulation of neurotransmitter release in the central nervous system and peripheral nervous system. The activation of these receptors by JWH-175 can lead to a variety of effects, including analgesia, anti-inflammatory effects, and psychoactive effects similar to those of tetrahydrocannabinol (THC), the active component of cannabis.
Legal Status
The legal status of JWH-175 varies by country. In many jurisdictions, it is classified as a controlled substance due to its potential for abuse and lack of medical use. The compound is often included in legislation targeting synthetic cannabinoids, which are frequently used as recreational drugs.
Synthesis
The synthesis of JWH-175 involves the condensation of a naphthoyl chloride with an indole derivative. This process is similar to the synthesis of other naphthoylindole compounds and requires careful control of reaction conditions to ensure the desired product is obtained.
Potential Uses
While JWH-175 and similar compounds have been primarily studied for their recreational use, there is ongoing research into their potential therapeutic applications. These include the treatment of chronic pain, neuropathic pain, and inflammatory disorders. However, the psychoactive effects and potential for abuse limit their use in clinical settings.
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