发明名称 CATHEPSIN CYSTEINE PROTEASE INHIBITORS
摘要 <p>The present invention relates to a novel class of compounds mainly, leucinamide-amino-carboxylate derivatives of formula (I) wherein Y is CR&lt;1&gt;R&lt;2&gt;, O, S, -SO2, C=0 or NR&lt;9&gt;; Z is CR&lt;1&gt;R&lt;2&gt;, O, S, -SO2, C=O or NR&lt;9&gt; and each G is independently a CR&lt;1&gt;CR&lt;2&gt;. Said compounds are cathepsin cysteine protease inhibitors, including but not limited to, inhibitors of cathepsin K, L, S and B and to pharmaceutical compositions thereof. These compounds are useful for treating and preventing cathepsin dependent conditions in which inhibition of bone resorption is indicated, such as osteoporosis.</p>
申请公布号 WO2005066159(A1) 申请公布日期 2005.07.21
申请号 WO2005CA00007 申请日期 2005.01.06
申请人 MERCK FROSST CANADA & CO.;BAYLY, CHRISTOPHER;BLACK, CAMERON;THERIEN, MICHEL 发明人 BAYLY, CHRISTOPHER;BLACK, CAMERON;THERIEN, MICHEL
分类号 A61K31/341;A61K31/40;A61K31/44;A61K31/4433;A61K31/445;A61K31/506;A61K31/55;A61P19/08;C07D207/24;C07D211/74;C07D213/65;C07D223/08;C07D307/32;C07D309/30;C07D401/04;C07D401/06;C07D401/12;C07D403/12;C07D405/12;C07D413/06;(IPC1-7):C07D403/12;A61K31/443 主分类号 A61K31/341
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