1. Academic Validation
  2. Discovery of SMP-304, a novel benzylpiperidine derivative with serotonin transporter inhibitory activity and 5-HT1A weak partial agonistic activity showing the antidepressant-like effect

Discovery of SMP-304, a novel benzylpiperidine derivative with serotonin transporter inhibitory activity and 5-HT1A weak partial agonistic activity showing the antidepressant-like effect

  • Bioorg Med Chem. 2017 Jan 1;25(1):293-304. doi: 10.1016/j.bmc.2016.10.034.
Hidefumi Yoshinaga 1 Shuji Masumoto 2 Koji Koyama 2 Naoya Kinomura 2 Yuji Matsumoto 2 Taro Kato 2 Satoko Baba 2 Kenji Matsumoto 2 Tomoko Horisawa 2 Hitomi Oki 2 Kazuki Yabuuchi 2 Toru Kodo 2
Affiliations

Affiliations

  • 1 Drug Research Division, Sumitomo Dainippon Pharma Co., Ltd., 33-94 Enoki-cho, Suita, Osaka 564-0053, Japan. Electronic address: hidefumi-yoshinaga@ds-pharma.co.jp.
  • 2 Drug Research Division, Sumitomo Dainippon Pharma Co., Ltd., 33-94 Enoki-cho, Suita, Osaka 564-0053, Japan.
Abstract

We report the discovery of a novel benzylpiperidine derivative with Serotonin Transporter (SERT) inhibitory activity and 5-HT1A receptor weak partial agonistic activity showing the antidepressant-like effect. The 3-methoxyphenyl group and the phenethyl group of compound 1, which has weak SERT binding activity, but potent 5-HT1A binding activity, were optimized, leading to compound 35 with potent and balanced dual SERT and 5-HT1A binding activity, but also potent CYP2D6 inhibitory activity. Replacement of the methoxy group in the left part of compound 35 with a larger alkoxy group, such as ethoxy, isopropoxy or methoxy-ethoxy group ameliorated CYP2D6 inhibition, giving SMP-304 as a candidate. SMP-304 with serotonin uptake inhibitory activity and 5-HT1A weak partial agonistic activity, which could work as a 5-HT1A antagonist, displayed faster onset of antidepressant-like effect than a representative SSRI paroxetine in an animal model.

Keywords

5-HT(1A) receptor; Antidepressant; Benzylpiperidine; Fast onset; Serotonin transporter.

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