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| 1 | KMI-008,a novel β-secretase inhibitor containing a hydroxymethylcarbonyl isostere as a transition-state mimic:design and synthesis of substrate-based octapeptides显示文摘 | Shuto D Kasai S Kimura T | 2003 | Bioorg Med Chem Lett2003，13，： | 1 |
| 2 | KMI-358 and KMI-370,highly potent and small-sized BACE1 inhibitors containing phenylnorstatine显示文摘 | Kimura T Shuto D Kasai S | 2004 | Bioorg Med Chem Lett2004，14，： | 1 |
| 3 | Design and synthesis of highly active Alzheimer's beta-secretase (BACE1)inhibitors,KMI-420 and KMI-429,with enhanced chemical stability显示文摘 | Kimura T Shuto D Hamada Y | 2005 | Bioorg Med Chem Lett2005，15，1： | 1 |
| 4 | Design and synthesis of highly active Alzheimer′s β-secretase (BACE1) inhibitors, KMI-420 and KMI-429, with enhanced chemical stability 显示文摘 | Kimura T Shuto D Hamada Y | 2005 | Bioorg Med Chem Lett2005，15，1： | 1 |
| 5 | KMI-008, a novel β-seeretase inhibitor containing a hydroxymethylcarbonyl isostere as a transitionstate mimic: design and synthesis of substrate-based octapeptides 显示文摘 | Shuto D Kasai S Kimura T | 2003 | Bioorg Med Chem Lett2003，13，： | 1 |
| 6 | KMI-008, a novel β-secretase inhibitor containing a hydoxymethylcarbonyl isostere as a transition-state mimic: design and synthesis of substrate-based octapeptides 显示文摘 | Shuto D Kasai S Kimura T | 2003 | Bioorg Med Chem Lett2003，13，24： | 1 |
| 7 | KMI-358 and KMI-370, highly potent and small-sized BACE1 inhibitors containing phenylnorstatine显示文摘 | Kimura T Shuto D Kasai S | 2004 | Bioorg Med Chem Lett2004，14，6： | 1 |
| 8 | Design and synthesis of highly active Alzheimer's β-secretase (BACE1) inhibittors, KMI-420 and KMI-429, with enhanced chemical stability显示文摘 | Kimura T Shuto D Hamada Y | 2005 | Bioorg Med Chem Lett2005，15，1： | 1 |
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