北海道大学大学院 薬学研究院 創薬科学研究教育センター 有機合成医薬学部門

研究業績

発表論文 2016年

  1. An oligodeoxyribonucleotide containing 5-formyl-2′-deoxycytidine (fC) at the CpG site forms a covalent complex with DNA cytosine-5 methyltransferases (DNMTs)

    Kousuke Sato, Kyoji Kawamoto, Shintaro Shimamura, Satoshi Ichikawa and Akira Matsuda*

    Bioorg. Med. Chem.. Lett2016, 26, 5395-5398. 

    DOI: 10.1016/j.bmcl.2016.10.040

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  2. 多成分反応を用いた天然物合成と構造活性相関研究
    千葉拓也、仲谷岳志、片山勝史、松田彰、市川聡
    有機合成化学協会誌 201674, 426-440
  3. Revisited Mechanistic Implications of the Joullié −Ugi ThreeComponent Reaction

    Akira Katsuyama, Akira Matsuda, and Satoshi Ichikawa*

    Org. Lett201618, 2552-2555. 

    DOI: 10.1021/acs.orglett.6b00827

    勝山さん OL joullie

  4. Chemical screening identifies EUrd as a novel inhibitor against Temozolomide-resistant glioblastoma-initiating cells.
    Yoshihiro Tsukamoto, Naoki Ohtsu, Smile Echizenya, Satoko Otsuguro, Ryosuke Ogura, Manabu Natsumeda, Mizuho Isogawa, Hiroshi Aoki, Satoshi Ichikawa, Masahiro Sakaitani, Akira Matsuda, Katsumi Maenaka, Yukihiko Fujii, Toru Kondo.*
    Stem Cells 2016accepted. DOI: 10.1002/stem.2380
  5. Design, Synthesis, and Biological Activity of Isosyringolin A

    Shun Kitahata, Takuya Chiba, Takashi Yoshida, Masaki Ri, Shinsuke Iida, Akira Matsuda, and Satoshi Ichikawa*

    Org. Lett., 2016, 18, 2312-2315.

    DOI: 10.1021/acs.orglett.6b01053

    Isosyringoin

  6. Structural insights into inhibition of lipid I production in bacterial cell wall synthesis

    Ben, C. Chung, Ellene, H. Mashalidis, Tetsuya, Tanino, Mijung, Kim, Akira, Matsuda, Jiyong, Hong, Satoshi, Ichikawa, Seok-Yong, Lee.*

    Nature, 2016533, 557-561. DOI: 10.1038/nature17636.

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  7. Design, synthesis and biological evaluation of a structurally simplified syringoin A Analogues

    Takuya, Chiba, Shun, Kitahata, Akira, Matsuda, Satoshi, Ichikawa.*

    Chem. Pharm. Bull. 2016, 64, 811-816.

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  8. Function-Oriented Synthesis: How to Design Simplified Analogues of Antibacterial Nucleoside Natural Products?

    Satoshi, Ichikawa*

    Chem. Rec. 201616, 1106-1115.

    DOI: 10.1002/tcr.201500247

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