Dinoxyline

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Overview[edit | edit source]

Dinoxyline is a synthetic compound that acts as a potent dopamine receptor agonist. It is primarily used in research settings to study the effects of dopamine receptor activation. Dinoxyline has a high affinity for the D1 and D2 subtypes of dopamine receptors, making it a valuable tool in neuropharmacology.

Chemical Structure[edit | edit source]

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Chemical structure of Dinoxyline

Dinoxyline is characterized by its unique chemical structure, which allows it to interact effectively with dopamine receptors. The structure of Dinoxyline includes a phenyl ring and a nitrogen-containing heterocycle, which are crucial for its binding affinity and activity.

Mechanism of Action[edit | edit source]

Dinoxyline functions by mimicking the action of dopamine, a neurotransmitter that plays a key role in the central nervous system. By binding to dopamine receptors, Dinoxyline can activate these receptors, leading to various physiological and behavioral effects. This makes it useful for studying conditions such as Parkinson's disease and schizophrenia, where dopamine signaling is disrupted.

Applications in Research[edit | edit source]

Due to its ability to selectively activate dopamine receptors, Dinoxyline is used extensively in research to:

  • Investigate the role of dopamine in neurotransmission
  • Study the effects of dopamine receptor activation on behavior and cognition
  • Develop new therapeutic agents for neurological disorders

Pharmacological Properties[edit | edit source]

Dinoxyline exhibits high potency and selectivity for dopamine receptors. Its pharmacological profile includes:

  • High affinity for D1 and D2 receptors
  • Ability to cross the blood-brain barrier
  • Long duration of action compared to endogenous dopamine

Safety and Toxicity[edit | edit source]

While Dinoxyline is a powerful research tool, it must be handled with care due to its potent effects on the central nervous system. Researchers must adhere to safety protocols to prevent unintended exposure and effects.

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Contributors: Prab R. Tumpati, MD