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3CL Protease Inhibitors with an Electrophilic Arylketone Moiety as Anti-SARS-CoV-2 Agents.
Konno S, Kobayashi K, Senda M, Funai Y, Seki Y, Tamai I, Schäkel L, Sakata K, Pillaiyar T, Taguchi A, Taniguchi A, Gütschow M, Müller CE, Takeuchi K, Hirohama M, Kawaguchi A, Kojima M, Senda T, Shirasaka Y, Kamitani W, Hayashi Y. Konno S, et al. Among authors: taniguchi a. J Med Chem. 2022 Feb 24;65(4):2926-2939. doi: 10.1021/acs.jmedchem.1c00665. Epub 2021 Jul 27. J Med Chem. 2022. PMID: 34313428
Development of Potent Myostatin Inhibitory Peptides through Hydrophobic Residue-Directed Structural Modification.
Takayama K, Rentier C, Asari T, Nakamura A, Saga Y, Shimada T, Nirasawa K, Sasaki E, Muguruma K, Taguchi A, Taniguchi A, Negishi Y, Hayashi Y. Takayama K, et al. Among authors: taniguchi a. ACS Med Chem Lett. 2017 Jun 6;8(7):751-756. doi: 10.1021/acsmedchemlett.7b00168. eCollection 2017 Jul 13. ACS Med Chem Lett. 2017. PMID: 28740611 Free PMC article.
Correction for Discovery of a Human Neuromedin U Receptor 1-Selective Hexapeptide Agonist with Enhanced Serum Stability.
Takayama K, Mori K, Tanaka A, Nomura E, Sohma Y, Mori M, Taguchi A, Taniguchi A, Sakane T, Yamamoto A, Minamino N, Miyazato M, Kangawa K, Hayashi Y. Takayama K, et al. Among authors: taniguchi a. J Med Chem. 2017 Sep 14;60(17):7613. doi: 10.1021/acs.jmedchem.7b01148. Epub 2017 Aug 18. J Med Chem. 2017. PMID: 28820261 No abstract available.
Design and synthesis of potent myostatin inhibitory cyclic peptides.
Rentier C, Takayama K, Saitoh M, Nakamura A, Ikeyama H, Taguchi A, Taniguchi A, Hayashi Y. Rentier C, et al. Among authors: taniguchi a. Bioorg Med Chem. 2019 Apr 1;27(7):1437-1443. doi: 10.1016/j.bmc.2019.02.019. Epub 2019 Feb 10. Bioorg Med Chem. 2019. PMID: 30777663
1,067 results