ACS Medicinal Chemistry Letters · 2021 · 70 citations · 34 references
MedicineNeurosciencePharmacologyDrug DiscoveryNeuropharmacologyPsychopharmacologyLigand BindingNeurotransmissionNeurotransmitter ReceptorsReceptor PharmacologySchizophrenia PharmacotherapySerotonergic Pharmacology5-Hydroxytryptamine 1A Receptor Agonists5-Hydroxytryptamine Receptor PharmacologyBreakthrough Therapy StrategyG Protein-coupled Receptor ModelingGlutamatergic NeurotransmissionMonoaminergic PathwaysSerotonin Receptor PharmacologySerotonin Receptor Subtypes
Ulotaront (SEP-363856) is a trace-amine associated receptor 1 (TAAR1) agonist with 5-HT1A receptor agonist activity in Phase 3 clinical development, with FDA Breakthrough Therapy Designation, for the treatment of schizophrenia. TAAR1 is a G-protein-coupled receptor (GPCR) that is expressed in cortical, limbic, and midbrain monoaminergic regions. It is activated by endogenous trace amines, and is believed to play an important role in modulating dopaminergic, serotonergic, and glutamatergic circuitry. TAAR1 agonism data are reported herein for ulotaront and its analogues in comparison to endogenous TAAR1 agonists. In addition, a human TAAR1 homology model was built around ulotaront to identify key interactions and attempt to better understand the scaffold-specific TAAR1 agonism structure-activity relationships.
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James R. Bunzow, Mark S. Sonders, Seksiri Arttamangkul et al. · Molecular Pharmacology · 2001 · 643 citations
Medicine, Neuroscience, Pharmacology +15
GPCRdb in 2021: integrating GPCR sequence, structure and function
Albert J. Kooistra, Stefan Mordalski, Gáspár Pándy‐Szekeres et al. · Nucleic Acids Research · 2020 · 376 citations · Full text