8篇
您的检索式：作者名="Kouketsu A"
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| 1 | Design, synthesis, structureselectivity relationship, and effect on human cancer cells of a novel series of histone deacetylase 6-selective inhibitors显示文摘 | Itoh Y Suzuki T Kouketsu A | 2007 | J Med Chem2007，50，22： | 1 |
| 2 | Highly potent and selective histone deacetylase 6 inhibitors designed based on a small-molecular substrate 显示文摘 | SUZUKI T KOUKETSU A ITOH Y | 2006 | J Med Chem2006，49，16： | 1 |
| 3 | Design,synthesis,structure-selectivity relationship,and effect on human cancer cells of a novel series of histone deacetylase 6-selective inhibitors显示文摘 | Itoh Y Suzuki T Kouketsu A | 2007 | J Med Chem2007，50，22： | 1 |
| 4 | Design, synthesis, structure-se- lectivity relationship, and effect on human cancer ceils of a novel series of histone deacetylase 6-selective inhibitors显示文摘 | Itoh Y Suzuki T Kouketsu A | 2007 | J Med Chem2007，50，22： | 1 |
| 5 | Design, synthesis, structure-selectivity relationship, and effect on human cancer cells of a novel series of histone deacetylase 6-selective inhibitors 显示文摘 | ITOH Y SUZUKI T KOUKETSU A | 2007 | J Med Chem2007，50，22： | 1 |
| 6 | Highly potent and selective histone deacetylase 6 inhibitors designed based on a small-molecular substrate 显示文摘 | SUZUKI T -KOUKETSU A ITOH Y | 2006 | J Med Chem2006，49，16： | 1 |
| 7 | Thiol-based SAHA analogues as potent histone deacetylase inhibitors 显示文摘 | SUZUKI T KOUKETSU A MATSUURA A | 2004 | Bioorg Med Chem Lett2004，14，12： | 1 |
| 8 | Identification of a potent non-hydroxamate histone deacetylase inhibitor by mechanism-based dury design显示文摘 | Suzuki T Matsuura A Kouketsu A | 2005 | Bioorg Med Chem Lett2005，15，2： | 1 |
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