LY-2183240

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LY-2183240_Structure.svg

LY-2183240 is a chemical compound that acts as a potent and selective inhibitor of the enzyme fatty acid amide hydrolase (FAAH). FAAH is responsible for the degradation of endocannabinoids, such as anandamide, which are involved in various physiological processes including pain, mood, and appetite regulation.

Mechanism of Action[edit | edit source]

LY-2183240 inhibits FAAH, leading to increased levels of endocannabinoids in the body. By preventing the breakdown of these signaling molecules, LY-2183240 enhances their effects on the endocannabinoid system. This system plays a crucial role in maintaining homeostasis and modulating various physiological functions.

Pharmacological Effects[edit | edit source]

The inhibition of FAAH by LY-2183240 results in elevated levels of anandamide and other endocannabinoids, which can produce analgesic, anti-inflammatory, and anxiolytic effects. These properties make LY-2183240 a potential therapeutic agent for conditions such as chronic pain, anxiety disorders, and inflammatory diseases.

Research and Development[edit | edit source]

LY-2183240 has been the subject of various preclinical studies to evaluate its efficacy and safety profile. These studies have demonstrated its potential in modulating pain and inflammation without the psychoactive effects associated with direct activation of cannabinoid receptors.

Potential Therapeutic Applications[edit | edit source]

Given its mechanism of action, LY-2183240 is being investigated for its potential use in treating a range of medical conditions, including:

Safety and Side Effects[edit | edit source]

While preclinical studies have shown promising results, the safety and side effect profile of LY-2183240 in humans is still under investigation. Potential side effects may include alterations in mood, appetite, and other physiological functions regulated by the endocannabinoid system.

Conclusion[edit | edit source]

LY-2183240 represents a novel approach to modulating the endocannabinoid system by inhibiting FAAH. Its potential therapeutic applications in pain management, anxiety, and inflammation highlight the importance of further research to fully understand its benefits and risks.

See Also[edit | edit source]

References[edit | edit source]

External Links[edit | edit source]

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Contributors: Prab R. Tumpati, MD