AR-M100390

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  1. AR-M100390

AR-M100390 is a synthetic compound that acts as a selective antagonist of the neuropeptide Y receptor Y1. This compound has been studied for its potential therapeutic applications in various conditions, including obesity, anxiety, and other disorders related to the neuropeptide Y system.

Chemical Structure and Properties[edit | edit source]

AR-M100390 is a small molecule with a specific chemical structure designed to selectively bind to the Y1 receptor subtype of the neuropeptide Y receptors. The precise molecular formula and structural details are proprietary, but it is known to have high affinity and selectivity for the Y1 receptor.

Mechanism of Action[edit | edit source]

Neuropeptide Y (NPY) is a 36-amino acid peptide neurotransmitter found in the brain and autonomic nervous system. It is involved in various physiological processes, including regulation of energy balance, memory, and anxiety. NPY exerts its effects through several receptor subtypes, including Y1, Y2, Y4, and Y5.

AR-M100390 functions as an antagonist at the Y1 receptor, meaning it binds to this receptor and inhibits its activation by endogenous NPY. By blocking the Y1 receptor, AR-M100390 can modulate the physiological effects mediated by this receptor, such as reducing appetite and anxiety.

Potential Therapeutic Applications[edit | edit source]

Research into AR-M100390 has explored its potential use in treating conditions such as:

  • **Obesity**: By antagonizing the Y1 receptor, AR-M100390 may help reduce appetite and food intake, contributing to weight loss.
  • **Anxiety Disorders**: The Y1 receptor is implicated in the regulation of anxiety. AR-M100390 may have anxiolytic effects by modulating this pathway.
  • **Other Disorders**: Given the broad role of NPY in the central nervous system, AR-M100390 may have potential in other neuropsychiatric and metabolic disorders.

Research and Development[edit | edit source]

AR-M100390 is primarily used in preclinical research to understand the role of the Y1 receptor in various physiological and pathological processes. Its development for clinical use would require extensive testing for safety and efficacy.

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