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Dopamine Agonists

总结
Researchers at Purdue University have developed new molecules that fully and selectively activate the dopamine D1 receptor. The compounds derived are useful for treating patients having a dopamine-related dysfunction of the central nervous system (CNS) as well as conditions in which peripheral dopamine receptors are involved. They are expected to be effective against Parkinson's disease, improving cognition, memory, attention deficit hyperactivity disorder, and related developmental disorders.
技术优势
Lead compound is 50 times more selective for D1 receptors than for D2L receptorsEquipotent, but more selective than other D1 agonists Potentially effective treatment for advanced Parkinson's disease and other CNS disordersOrally bioavailable in animal models
技术应用
Medical/HealthcarePharmaceuticalsDrug Development
详细技术说明
David NicholsPurdue Medicinal Chemistry and Molecular Pharmacology
*Abstract

*Background
Dopamine is a neurotransmitter in the central nervous system that has been implicated in numerous neurological disorders. For example, excess stimulation of dopamine may be linked to schizophrenia, whereas either excessive or insufficient functional dopaminergic activity may cause hypertension, narcolepsy, and other disorders including Parkinson's disease. The D1 receptor is a dopamine receptor subtype that may be a viable therapeutic target for dopamine-related pathologies. Accordingly, researchers have directed their efforts to design ligands that are selective D1 receptor agonists.
*IP Issue Date
Nov 27, 2012
*IP Type
Utility
*Stage of Development
Proof of Concept
*Web Links
Purdue Office of Technology CommercializationPurdueInnovation and EntrepreneurshipDavid NicholsPurdue Medicinal Chemistry and Molecular Pharmacology
国家
United States
申请号码
8,318,938
国家/地区
美国

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