发明名称 N-HYDROXY-NAPHTHALENE DICARBOXAMIDE AND N-HYDROXY-BIPHENYL-DICARBOXAMIDE COMPOUNDS AS HISTONE DEACETYLASE INHIBITORS
摘要 <p>The present invention relates to a novel class of N-hydroxy-naphthalene dicarboxamide and N-hydroxy-biphenyl-dicarboxamide derivatives. The N-hydroxy-naphthalene dicarboxamide and N-hydroxy-biphenyl-dicarboxamide compounds can be used to treat cancer. The N-hydroxy-naphthalene dicarboxamide and N-hydroxy-biphenyl-dicarboxamide compounds can also inhibit histone deacetylase and are suitable for use in selectively inducing terminal differentiation, and arresting cell growth and/or apoptosis of neoplastic cells, thereby inhibiting proliferation of such cells. Thus, the compounds of the present invention are useful in treating a patient having a tumor characterized by proliferation of neoplastic cells. The compounds of the invention may also be useful in the prevention and treatment of TRX-mediated diseases, such as autoimmune, allergic and inflammatory diseases, and in the prevention and/or treatment of diseases of the central nervous system (CNS), such as neurodegenerative diseases. The present invention further provides pharmaceutical compositions comprising the N-hydroxy-naphthalene dicarboxamide and N-hydroxy-biphenyl-dicarboxamide derivatives and safe dosing regimens of these pharmaceutical compositions, which are easy to follow, and which result in a therapeutically effective amount of the N-hydroxy-naphthalene dicarboxamide and N-hydroxy-biphenyl-dicarboxamide derivatives in vivo.</p>
申请公布号 WO2009045385(A1) 申请公布日期 2009.04.09
申请号 WO2008US11289 申请日期 2008.09.30
申请人 MERCK & CO., INC.;SURDI, LAURA;KATTAR, SOLOMON;MILLER, THOMAS, A.;OTTE, KARIN, M.;SILIPHAIVANH, PHIENG;TEMPEST, PAUL;ZABIEREK, ANNA, A. 发明人 KATTAR, SOLOMON;MILLER, THOMAS, A.;OTTE, KARIN, M.;SILIPHAIVANH, PHIENG;SURDI, LAURA;TEMPEST, PAUL;ZABIEREK, ANNA, A.
分类号 A01N37/18;A61K31/16 主分类号 A01N37/18
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