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 2019年

  1. Synthesis and biological evaluation of MraY selective analogue of tunicamycins

    Kazuki Yamamoto, Toyotaka Sato, Yuta Hikiji, Akira Katsuyama, Takanori Matsumaru, Fumika Yakushiji, Shin-ichi Yokota, and Satoshi Ichikawa*

    Nucleosides, Nucleotides & Nucleic Acids 2019, accepted

    DOI: https://doi.org/10.1080/15257770.2019.1649696

     

  2. Novel adenosine-derived inhibitors of Cryptosporidium parvum inosine 5’-monophosphate dehydrogenase

    Kengo Shigetomi, Albertus Eka Yudistira Sarwono, Satoshi Ichikawa, Makoto Ubukata*

    J. Antibiot. 2019, 72, 934-942.

    DOI: https://doi.org/10.1038/s41429-019-0199-3

     

  3. Polycomb Repressive Complex 2: Modulator Development for Functional Regulation of a Multiprotein Complex by Using Structural Information

    Yasuaki Tokodai, Fumika Yakushiji

    ChemBioChem 2019, 20, 2046-2053.

    DOI: 10.1002/cbic.201900212

     

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  4. Chemical logic of MraY inhibition by antibacterial nucleoside natural products

    Ellene H. Mashalidis, Benjamin Kaeser, Yuma Terasawa, Akira Katsuyama, Do-Yeon Kwon, Kiyoun Lee, Jiyong Hong, Satoshi Ichikawa, Seok-Yong Lee

    Nat. Commun. 2019, 10, 2917.

    DOI: 10.1038/s41467-019-10957-9

     

  5. Tunicamycin: Chemical synthesis and biosynthesis

    Kazuki Yamamoto, Satoshi Ichikawa

    J. Antibiot. 2019, 72, 924-933.

    DOI: 10.1038/s41429-019-0200-1

     

  6. Synthesis of All Stereoisomers of Monomeric Spectomycin A1/A2 and Evaluation of Their Protein SUMOylation‐Inhibitory Activity

    Yusaku Nomura, Frédéric Thuaud, Daisuke Sekine, Akihiro Ito, Satoko Maeda, Hiroyuki Koshino, Daisuke Hashizume, Atsuya Muranaka, Thomas Cruchter, Masanobu Uchiyama, Satoshi Ichikawa, Akira Matsuda, Minoru Yoshida, Go Hirai*, Mikiko Sodeoka*
    Chem. Eur. J. 201925, 8387–8392.

    DOI: 10.1002/chem.201901093

     

  7. Structual requirement of tunicamycin V for MraY inhibition

    Kazuki Yamamoto; Akira Katsuyama and Satoshi Ichikawa

    Bioorg. Med. Chem. 2019, 1714-1719.

    DOI: 10.1016/j.bmc.2019.02.035

     

    1-s2.0-S0968089618318133-ga1

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