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[文献書誌] Y.Hamada, H.Matsumoto, T.Kimura, Y.Hayashi, Y.Kiso: "Effect of the acyl groups on O→N acyl migration in the water-soluble prodrugs of HIV-1 protease inhibitor."Biorg.Med.Chem.Lett.. 13(16). 2727-2730 (2003)
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[文献書誌] A.Nezami, T.Kimura, K.Hidaka, A.Kiso, J.Liu, Y.Kiso, E.Freire, et al.: "High affinity inhibition of a family of Plasmodium falciparum proteases by a designed adaptive inhibitor"Biochemistry. 42(28). 8459-8464 (2003)
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[文献書誌] Y.Sohma, Y.Hayashi, T.Ito, H.Matsumoto, T.Kimura, Y.Kiso: "Development of water-soluble prodrugs of the HIV-1 protease inhibitor KNI-727"J.Med.Chem.. 46(19). 4124-4135 (2003)
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[文献書誌] D.Shuto, S.Kasai, T.Kimura, P.Liu, K.Hidaka, T.Hamada, et al.: "KMI-008, a novel β-secretase inhibitor containing a hydroxymethylcarbonyl isostere as a transition-state mimic : design and synthesis of substrate-based octapeptides"Biorg.Med.Chem.Lett.. 13(24). 4273-4276 (2003)
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[文献書誌] Y.Hamada, H.Matsumoto, S.Yamaguchi, T.Kimura, Y.Hayashi, et al.: "Water-soluble prodrugs of dipeptide HIV protease inhibitors based on O-N intramolelcular acyl migration : design, synthesis and kinetic study"Biorg.Med.Chem.. 12(1). 159-170 (2004)
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[文献書誌] T.Kimura, D.Shuto, S.Kasai, P.Liu, K.Hidaka, T.Hamada, Y.Hayashi, et al.: "KMI-358 and KMI-370, highly potent and small-sized BACE1 inhibitors containing phenylnorstatine"Biorg.Med.Chem.Lett.. 14(6). 1527-1531 (2004)
