1. Academic Validation
  2. Discovery of DS34942424: An orally potent analgesic without mu opioid receptor agonist activity

Discovery of DS34942424: An orally potent analgesic without mu opioid receptor agonist activity

  • Bioorg Med Chem. 2020 Nov 1;28(21):115714. doi: 10.1016/j.bmc.2020.115714.
Tsuyoshi Arita 1 Masayoshi Asano 2 Kazufumi Kubota 3 Yuki Domon 3 Nobuo Machinaga 4 Kousei Shimada 4
Affiliations

Affiliations

  • 1 Medicinal Chemistry Research Laboratories, R&D Division, Daiichi Sankyo Co., Ltd., 1-2-58 Hiromachi, Shinagawa-ku, Tokyo 140-8710, Japan. Electronic address: [email protected].
  • 2 Intellectual Property Department, Global Brand Strategy Division, Daiichi Sankyo Co., Ltd., 1-2-58 Hiromachi, Shinagawa-ku, Tokyo 140-8710, Japan.
  • 3 Specialty Medicine Research Laboratories, R&D Division, Daiichi Sankyo Co., Ltd., 1-2-58 Hiromachi, Shinagawa-ku, Tokyo 140-8710, Japan.
  • 4 Medicinal Chemistry Research Laboratories, R&D Division, Daiichi Sankyo Co., Ltd., 1-2-58 Hiromachi, Shinagawa-ku, Tokyo 140-8710, Japan.
Abstract

We identified (5'S)-10'-fluoro-6'-methyl-5',6'-dihydro-3'H-spiro[cyclopropane-1,4'-[2,6]diaza[2,5]methano[2,6]benzodiazonin]-7'(1'H)-one, 22b (DS34942424) with a unique and original bicyclic skeleton. 22b showed an orally potent analgesic in the acetic acid-induced writhing test and formalin test in ddY mice without sedation. Moreover, 22b did not exhibit mu Opioid Receptor Agonist activity.

Keywords

Alkaloid; Analgesic; Conolidine; Non-opioid analgesics.

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