Cathepsin cysteine protease inhibitors
    13.
    发明申请
    Cathepsin cysteine protease inhibitors 审中-公开
    组织蛋白酶半胱氨酸蛋白酶抑制剂

    公开(公告)号:US20090176861A1

    公开(公告)日:2009-07-09

    申请号:US10585144

    申请日:2005-01-06

    CPC分类号: C07D207/273 C07D307/33

    摘要: The present invention relates to a novel class of compounds mainly, substituted leucinamide-carboxylate derivatives of formula (I) wherein X is O or NR9, Y is CR1R2, —SO2, C═O or NR9; Z is CR1R2, O, S, —SO2 or NR9 and each G is independently a CR1CR2 and pharmaceutical compositions thereof. Said compounds are cathepsin cysteine protease inhibitors, including but not limited to, inhibitors of cathepsin K, L, S and B. These compounds are useful for treating and preventing cathepsin dependent conditions in which inhibition of bone resorption is indicated, such as osteoporosis.

    摘要翻译: 本发明涉及一类新的化合物,主要是其中X是O或NR 9,Y是CR 1 R 2,-SO 2,C-O或NR 9的式(I)的取代的亮氨酰胺羧酸酯衍生物; Z是CR1R2,O,S,-SO2或NR9,每个G独立地是CR1CR2及其药物组合物。 所述化合物是组织蛋白酶半胱氨酸蛋白酶抑制剂,包括但不限于组织蛋白酶K,L,S和B的抑制剂。这些化合物可用于治疗和预防组织蛋白酶依赖性条件,其中指出了骨吸收的抑制,例如骨质疏松症。

    Cathepsin Cysteine Protease Inhibitors
    19.
    发明申请
    Cathepsin Cysteine Protease Inhibitors 审中-公开
    组织蛋白酶半胱氨酸蛋白酶抑制剂

    公开(公告)号:US20090253672A1

    公开(公告)日:2009-10-08

    申请号:US12083474

    申请日:2006-10-10

    CPC分类号: C07K5/06191 A61K38/00

    摘要: This invention relates to a novel class of compounds, represented by the formula (I) below, wherein the meanings of R1, R2, R3, R4, R5, R6, R7, X and Y are indicated therein, which are cysteine protease inhibitors, including but not limited to, inhibitors of cathepsms K L, S and B These compounds are useful for treating diseases in which inhibition of bone resorption is indicated, such as osteoporosis, osteoarthritis and rheumatoid arthritis

    摘要翻译: 本发明涉及由下式(I)表示的新一类化合物,其中R 1,R 2,R 3,R 4,R 5,R 6,R 7,X和Y的含义在其中表示,它们是半胱氨酸蛋白酶抑制剂, 包括但不限于组织蛋白酶KL,S和B的抑制剂。这些化合物可用于治疗其中指示骨吸收抑制的疾病,例如骨质疏松症,骨关节炎和类风湿性关节炎