4.6 Article

Knowledge-Based Design of Long-Chain Arylpiperazine Derivatives Targeting Multiple Serotonin Receptors as Potential Candidates for Treatment of Autism Spectrum Disorder

Journal

ACS CHEMICAL NEUROSCIENCE
Volume 12, Issue 8, Pages 1313-1327

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acschemneuro.0c00647

Keywords

5-HT7 receptor; 5-HT1A receptor; 5-HT2A receptor; arylpiperazine; autism spectrum disorder; knowledge-based design

Funding

  1. Telethon Foundation [GGP13145]
  2. German Research Foundation (DFG) [PO732, ZE994/2]
  3. Spanish Ministry of Economy and Competitiveness (MINECO) [SAF2014-57138-C2-1-R]
  4. Xunta de Galicia (Centro singular de investigacion de Galicia accreditation) [ED431G 2019/02]
  5. European Union (European Regional Development Fund - ERDF)
  6. COST Action [CA18133]

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Autism spectrum disorder (ASD) is a group of neurodevelopmental disorders with no effective treatments currently available. Studies show that targeting the brain serotonin system may help treat core symptoms of ASD and associated intellectual disabilities. New compounds with 5-HT receptor properties have been synthesized and show promise for future ASD treatments.
Autism spectrum disorder (ASD) includes a group of neurodevelopmental disorders characterized by core symptoms such as impaired social interaction and communication, repetitive and stereotyped behaviors, and restricted interests. To date, there are no effective treatments for these core symptoms. Several studies have shown that the brain serotonin (5-HT) neurotransmission system is altered in both ASD patients and animal models of the disease. Multiple pieces of evidence suggest that targeting 5-HT receptors may treat the core symptoms of ASD and associated intellectual disabilities. In fact, stimulation of the 5-HT1A receptor reduces repetitive and restricted behaviors; blockade of the 5-HT2A receptor reduces both learning deficits and repetitive behavior, and activation of the 5-HT7 receptor improves cognitive performances and reduces repetitive behavior. On such a basis, we have designed novel arylpiperazine derivatives pursuing unprecedently reported activity profiles: dual 5-HT7/5-HT1A receptor agonist properties and mixed 5-HT7 agonist/5-HT1A agonist/5-HT2A antagonist properties. Seventeen new compounds were synthesized and tested in radioligand binding assay at the target receptors. We have identified the dual 5-HT1AR/5-HT7R agonists 8c and 29 and the mixed 5-HT1AR agonist/5-HT7R agonist/5-HT2AR antagonist 20b. These compounds are metabolically stable in vitro and have suitable central nervous system druglike properties.

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