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  1. 1
    Synthesis and glycosidase inhibition of 5-C-alkyl-DNJ and 5-C-alkyl-l-ido-DNJ derivatives

    Synthesis and glycosidase inhibition of 5-C-alkyl-DNJ and 5-C-alkyl-l-ido-DNJ derivatives von Lu, Tian-Tian, Shimadate, Yuna, Cheng, Bin, Kanekiyo, Uta, Kato, Atsushi, Wang, Jun-Zhe, Li, Yi-Xian, Jia, Yue-Mei, Fleet, George W.J., Yu, Chu-Yi


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  2. 2
    5‑C‑Branched Deoxynojirimycin: Strategy for Designing a 1‑Deoxynojirimycin-Based Pharmacological Chaperone with a Nanomolar Affinity for Pompe Disease

    5‑C‑Branched Deoxynojirimycin: Strategy for Designing a 1‑Deoxynojirimycin-Based Pharmacological Chaperone with a Nanomolar Affinity for Pompe Disease von Kato, Atsushi, Nakagome, Izumi, Kanekiyo, Uta, Lu, Tian-Tian, Li, Yi-Xian, Yoshimura, Kosuke, Kishida, Mana, Shinzawa, Kenta, Yoshida, Tomoki, Tanaka, Nobutada, Jia, Yue-Mei, Nash, Robert J, Fleet, George W. J, Yu, Chu-Yi

    Veröffentlicht in Journal of medicinal chemistry

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  3. 3
    Introduction of -alkyl branches to -iminosugars changes their active site binding orientation

    Introduction of -alkyl branches to -iminosugars changes their active site binding orientation von Kato, Atsushi, Nakagome, Izumi, Yoshimura, Kosuke, Kanekiyo, Uta, Kishida, Mana, Shinzawa, Kenta, Lu, Tian-Tian, Li, Yi-Xian, Nash, Robert J, Fleet, George W. J, Tanaka, Nobutada, Yu, Chu-Yi


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  4. 4
    Introduction of C -alkyl branches to l -iminosugars changes their active site binding orientation

    Introduction of C -alkyl branches to l -iminosugars changes their active site binding orientation von Kato, Atsushi, Nakagome, Izumi, Yoshimura, Kosuke, Kanekiyo, Uta, Kishida, Mana, Shinzawa, Kenta, Lu, Tian-Tian, Li, Yi-Xian, Nash, Robert J., Fleet, George W. J., Tanaka, Nobutada, Yu, Chu-Yi


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