发明名称 Leucinamide derivatives suitable as cathepsin cysteine protease inhibitors
摘要 Leucinamide derivative compounds of formula (I) which are cathepsin cysteine protease inhibitors, particularly inhibitors of cathepsins K, L, S and B are disclosed , wherein the substituents for the variables shown in formula (I) are as defined in the specification. These compounds are useful for treating diseases in which inhibition of bone resorption is indicated, such as osteoporosis, glucocorticoid induced osteoporosis, Paget's disease, abnormally increased bone turnover, periodontal disease, tooth loss, bone fractures, rheumatoid arthritis, osteoarthritis, periprosthetic osteolysis, osteogenesis imperfecta, metastatic bone disease, hypercalcemia of malignancy and multiple myeloma.
申请公布号 NZ534583(A) 申请公布日期 2006.11.30
申请号 NZ20030534583 申请日期 2003.02.28
申请人 AXYS PHARMACEUTICALS, INC 发明人 BAYLY, CHRISTOPHER I;BLACK, CAMERON;LEGER, SERGE;LI, CHUNG SING;MCKAY, DAN;MELLON, CHRISTOPHE;GAUTHIER, JACQUES YVES;LAU, CHEUK;THERIEN, MICHEL;TRUONG, VOUY-LINH;GREEN, MICHAEL J;HIRSCHBEIN, BERNARD L;JANC, JAMES W;PALMER, JAMES T;BASKARAN, CHITRA
分类号 C07D295/12;A61K31/275;A61K31/381;A61K31/404;A61K31/417;A61K31/42;A61K31/4245;A61K31/426;A61K31/427;A61K31/44;A61K31/4406;A61K31/4409;A61K31/4465;A61K31/47;A61K31/495;A61K31/505;A61K31/5375;A61K45/00;A61P1/02;A61P3/14;A61P19/02;A61P19/08;A61P19/10;A61P29/00;A61P35/00;A61P43/00;C07C255/25;C07C255/29;C07C255/46;C07C255/58;C07C255/60;C07C259/10;C07C311/37;C07C317/32;C07C317/36;C07D209/08;C07D211/26;C07D211/38;C07D213/36;C07D213/38;C07D213/57;C07D213/61;C07D213/64;C07D213/70;C07D213/71;C07D213/74;C07D213/89;C07D215/12;C07D231/12;C07D233/54;C07D233/64;C07D239/06;C07D239/26;C07D241/12;C07D261/08;C07D263/32;C07D271/06;C07D277/28;C07D295/135;C07D295/22;C07D307/52;C07D333/20;C07D401/04;C07D417/04;(IPC1-7):A61K31/275 主分类号 C07D295/12
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