Discovery of Trace Amine Associated Receptor 1 (TAAR1) Agonist 2-(5-(4'-Chloro-[1,1'-biphenyl]-4-yl)-4 H-1,2,4-triazol-3-yl)ethan-1-amine (LK00764) for the Treatment of Psychotic Disorders

Biomolecules. 2022 Nov 7;12(11):1650. doi: 10.3390/biom12111650.

Abstract

A focused in-house library of about 1000 compounds comprising various heterocyclic motifs in combination with structural fragments similar to β-phenethylamine (PEA) or tyramine was screened for the agonistic activity towards trace amine-associated receptor 1 (TAAR1). The screening yielded two closely related hits displaying EC50 values in the upper submicromolar range. Extensive analog synthesis and testing for TAAR1 agonism in a BRET-based cellular assay identified compound 62 (LK00764) with EC50 = 4.0 nM. The compound demonstrated notable efficacy in such schizophrenia-related in vivo tests as MK-801-induced hyperactivity and spontaneous activity in rats, locomotor hyperactivity of dopamine transporter knockout (DAT-KO) rats, and stress-induced hyperthermia (i.p. administration). Further preclinical studies are necessary to evaluate efficacy, safety and tolerability of this potent TAAR1 agonist for the potential development of this compound as a new pharmacotherapy option for schizophrenia and other psychiatric disorders.

Keywords: 1,2,4-triazoles; agonism; dopamine transporter knockout rats; dopamine, MK-801-induced hyperactivity; locomotor hyperactivity; schizophrenia; spontaneous activity; stress-induced hyperthermia; trace amine associated receptor 1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biphenyl Compounds
  • Psychotic Disorders*
  • Rats
  • Receptors, G-Protein-Coupled* / agonists

Substances

  • Trace amine-associated receptor 1
  • biphenyl
  • Receptors, G-Protein-Coupled
  • Biphenyl Compounds

Grants and funding

This research was supported by the Russian Science Foundation (grant no. 19-75-30008).