Melanin-concentrating hormone receptor antagonists and compositions and methods related thereto
    4.
    发明申请
    Melanin-concentrating hormone receptor antagonists and compositions and methods related thereto 审中-公开
    黑色素浓集激素受体拮抗剂及其组合物和方法

    公开(公告)号:US20050176738A1

    公开(公告)日:2005-08-11

    申请号:US10982696

    申请日:2004-11-05

    CPC分类号: C07D495/04

    摘要: Melanin-concentrating hormone (MCH) receptor antagonists are disclosed having utility for the treatment of MCH receptor-based disorders such as obesity. The compounds of this invention have the following structure: including pharmaceutically acceptable salts, esters, solvates, stereoisomers, and prodrugs thereof, wherein m, n, Q1, Q2, R1, R2, R3, R4, R7 and X are as defined herein. Also disclosed are compositions containing a compound of this invention, as well as methods relating to the use thereof.

    摘要翻译: 公开了用于治疗基于MCH受体的疾病如肥胖症的黑色素浓缩激素(MCH)受体拮抗剂。 本发明的化合物具有以下结构:其药学上可接受的盐,酯,溶剂合物,立体异构体和前药,其中m,n,Q 1,Q 2, R 1,R 2,R 3,R 4,R 7和R 7, X如本文所定义。 还公开了含有本发明化合物的组合物以及与其用途有关的方法。

    Tri-peptide Inhibitors of Serine Elastases
    5.
    发明申请
    Tri-peptide Inhibitors of Serine Elastases 审中-公开
    丝氨酸弹性蛋白酶的三肽抑制剂

    公开(公告)号:US20090156509A1

    公开(公告)日:2009-06-18

    申请号:US12326612

    申请日:2008-12-02

    IPC分类号: A61K38/06 C07K5/097

    摘要: The present invention provides compounds of formula (I): where X is R1—(CR3R4)nOC(O)—; R1—(CR3R4)nC(O)—; R1—C(O)NH(CR3R4)nOC(O)—; R1—C(O)NH(CR3R4)nC(O)—; R1—C(O)(CR3R4)nOC(O)—; or R1—C(O)(CR3R4)nC(O)—; where R1 is optionally substituted C5-10 aryl or heteroaryl; OH or NH2; where R3 and R4 are independently H or methyl; and n is 0 to 6; and Y is —CF3 or one of: where R2 is C1-8 alkyl optionally substituted with halo or —OH; —(CR6R7)p—C5-6 aryl optionally substituted with halo, —OH, C1-8 alkyl, C1-8 haloalkyl, —(CH2)mC(O)NH2 or —(CH2)mOCH3; where R6 and R7 are independently H or methyl; m is 0 to 4, and p is 0 or 1 or a pharmaceutically acceptable salt, ester, metabolite or prodrug thereof

    摘要翻译: 本发明提供式(I)化合物:其中X为R1-(CR3R4)nOC(O) - ; R1-(CR3R4)nC(O) - ; R1-C(O)NH(CR3R4)nOC(O) - ; R1-C(O)NH(CR3R4)nC(O) - ; R1-C(O)(CR3R4)nOC(O) - ; 或R 1 -C(O)(CR 3 R 4)n C(O) - ; 其中R 1是任选取代的C 5-10芳基或杂芳基; OH或NH2; 其中R3和R4独立地是H或甲基; n为0〜6; 并且Y是-CF 3或其中R 2是任选被卤素或-OH取代的C 1-8烷基之一; -OH,C 1-8烷基,C 1-8卤代烷基, - (CH 2)m C(O)NH 2或 - (CH 2)m OCH 3) - (CR 6 R 7) 其中R 6和R 7独立地为H或甲基; m为0至4,p为0或1或其药学上可接受的盐,酯,代谢物或前药