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Development of a novel class of peroxisome proliferator-activated receptor (PPAR) gamma ligands as an anticancer agent with a unique binding mode based on a non-thiazolidinedione scaffold.
Yamamoto K, Tamura T, Nakamura R, Hosoe S, Matsubara M, Nagata K, Kodaira H, Uemori T, Takahashi Y, Suzuki M, Saito JI, Ueno K, Shuto S. Yamamoto K, et al. Among authors: shuto s. Bioorg Med Chem. 2019 Nov 15;27(22):115122. doi: 10.1016/j.bmc.2019.115122. Epub 2019 Sep 16. Bioorg Med Chem. 2019. PMID: 31623970 Free article.
Nucleosides and nucleotides. 175. Structural requirements of the sugar moiety for the antitumor activities of new nucleoside antimetabolites, 1-(3-C-ethynyl-beta-D-ribo-pentofuranosyl)cytosine and -uracil1.
Hattori H, Nozawa E, Iino T, Yoshimura Y, Shuto S, Shimamoto Y, Nomura M, Fukushima M, Tanaka M, Sasaki T, Matsuda A. Hattori H, et al. Among authors: shuto s. J Med Chem. 1998 Jul 16;41(15):2892-902. doi: 10.1021/jm9801814. J Med Chem. 1998. PMID: 9667977
Synthesis of derivatives of (1S,2R)-1-phenyl-2-[(S)-1-aminopropyl]-N,N-diethylcyclopropanecarboxamide (PPDC) modified at the 1-aromatic moiety as novel NMDA receptor antagonists: the aromatic group is essential for the activity.
Kazuta Y, Tsujita R, Yamashita K, Uchino S, Kohsaka S, Matsuda A, Shuto S. Kazuta Y, et al. Among authors: shuto s. Bioorg Med Chem. 2002 Dec;10(12):3829-48. doi: 10.1016/s0968-0896(02)00346-2. Bioorg Med Chem. 2002. PMID: 12413836
254 results