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Journal of the American Chemical Society|April 3, 2003
Total synthesis of leustroducsin BKousei Shimada, Yosuke Kaburagi, Tohru FukuyamaBioorganic & Medicinal Chemistry Letters|August 7, 2019
Discovery of novel PTHR1 antagonists: Design, synthesis, and structure activity relationshipsYoshikazu Arai, Yohei Kiyotsuka, Kousei Shimada, et al.Bioorganic & Medicinal Chemistry Letters|June 1, 2019
Discovery of conolidine derivative DS39201083 as a potent novel analgesic without mu opioid agonist activityTsuyoshi Arita, Masayoshi Asano, Kazufumi Kubota, et al.Bioorganic & Medicinal Chemistry Letters|November 3, 2019
Discovery of a novel bicyclic compound, DS54360155, as an orally potent analgesic without mu-opioid receptor agonist activityTsuyoshi Arita, Masayoshi Asano, Kazufumi Kubota, et al.Bioorganic & Medicinal Chemistry|October 16, 2020
Discovery of DS34942424: An orally potent analgesic without mu opioid receptor agonist activityTsuyoshi Arita, Masayoshi Asano, Kazufumi Kubota, et al.Bioorganic & Medicinal Chemistry Letters|December 29, 2005
4-Aminophenoxyacetic acids as a novel class of reversible cathepsin K inhibitorsTsuyoshi Shinozuka, Kousei Shimada, Satoshi Matsui, et al.Bioorganic & Medicinal Chemistry Letters|January 17, 2021
A novel [5.2.1]bicyclic amine is a potent analgesic without µ opioid activityTetsuji Noguchi, Yuma Umezaki, Rieko Takano, et al.Bioorganic & Medicinal Chemistry|July 11, 2006
Arylamine based cathepsin K inhibitors: investigating P3 heterocyclic substituentsTsuyoshi Shinozuka, Kousei Shimada, Satoshi Matsui, et al.Bioorganic & Medicinal Chemistry|March 5, 2013
Discovery and structure-activity relationship of thienopyridine derivatives as bone anabolic agentsKeiji Saito, Akira Nakao, Tsuyoshi Shinozuka, et al.Bioorganic & Medicinal Chemistry Letters|May 13, 2018
Alkylsulfanyl analogs as potent α2δ ligandsKousei Shimada, Yasuo Ohata, Jun Kobayashi, et al.Pageof 2