4.7 Article

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

期刊

BIOORGANIC & MEDICINAL CHEMISTRY
卷 26, 期 20, 页码 5538-5546

出版社

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

关键词

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

资金

  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]

向作者/读者索取更多资源

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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