4.6 Article

Identification of a Potent Human Trace Amine-Associated Receptor1 Antagonist

期刊

ACS CHEMICAL NEUROSCIENCE
卷 13, 期 7, 页码 1082-1095

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acschemneuro.2c00086

关键词

trace amine-associated receptor 1 antagonist; cAMP functional assay; structure-activity relationship; Parkinson's disease; dopaminergic neurons; spontaneous firing rate

资金

  1. National Institute of Neurological Disorders and Stroke of the National Institutes of Health [R03NS116577]
  2. RTI International research and development funds
  3. Canada Research Chair Tier 1 grant [950-232211]
  4. Canadian Institutes of Health Research grant [FDN-147473]
  5. National Institute of Mental Health's Psychoactive Drug Screening Program [HHSN-271-2018-00023-C]

向作者/读者索取更多资源

The article reports the discovery of a hTAAR1 antagonist with potential for disease treatment, showing good pharmacological effects and mechanisms.
Human trace amine-associated receptor subtype 1 (hTAAR1) is a G protein-coupled receptor that has therapeutic potential for multiple diseases, including schizophrenia, drug addiction, and Parkinson's disease (PD). Although several potent agonists have been identified and have shown positive results in various clinical trials for schizophrenia, the discovery of potenthTAAR1 antagonists remains elusive. Herein, we report the results of structure-activity relationship studies that have led to the discovery of a potent hTAAR1 antagonist (RTI-7470-44,34). RTI-7470-44 exhibited an IC50of 8.4 nM in anin vitrocAMP functional assay, aKiof 0.3 nMin a radioligand binding assay, and showed species selectivity for hTAAR1 over the rat and mouseorthologues. RTI-7470-44 displayed good blood-brain barrier permeability, moderate metabolicstability, and a favorable preliminary off-target profile. Finally, RTI-7470-44 increased the spontaneousfiring rate of mouse VTA dopaminergic neurons and blocked the effects of the known TAAR1 agonist RO5166017.Collectively, this work provides a promising hTAAR1 antagonist probe that can be used to study TAAR1 pharmacology and the potential therapeutic role in hypodopaminergic diseases such as PD

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