4.7 Article

Design, synthesis, and systematic evaluation of 4-arylpiperazine- and 4-benzylpiperidine napthyl ethers as inhibitors of monoamine neurotransmitters reuptake

Journal

BIOORGANIC & MEDICINAL CHEMISTRY
Volume 26, Issue 20, Pages 5538-5546

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmc.2018.09.033

Keywords

Depression; 4-Arylpiperazine; 4-Benzylpiperidine; Naphthyl ether; Serotonin reuptake inhibitor; Norepinephrine reuptake inhibitor; Docking

Funding

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education [2012R1A1A2006613]
  2. Bio & Medical Technology Development Program of the National Research Foundation (NRF)
  3. Korean government (MSIT) [NRF-2017M3A9G2077568]

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Two series of 4-arylpiperazine- and 4-benzylpiperidine naphthyl ethers were designed based on structure-activity relationship (SAR) and docking model of reported monoamine neurotransmitters reuptake inhibitors. The compounds were synthesized in 3-simple steps and their biological activities were evaluated. Several compounds were proven to be potent inhibitors of serotonin and norepinephrine reuptake. Computer docking was performed to study the interaction of the most potent compound 35 with human serotonin transporter. The results of the analyses suggest that 4-arylpiperazine- and 4-benzylpiperidine naphthyl ethers might be promising anti-depressants worthy of further studies.

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