1H-pyrrolo [2,3-D] pyrimidine derivatives and methods of use thereof
    3.
    发明授权
    1H-pyrrolo [2,3-D] pyrimidine derivatives and methods of use thereof 有权
    1H-吡咯并[2,3-D]嘧啶衍生物及其使用方法

    公开(公告)号:US07429596B2

    公开(公告)日:2008-09-30

    申请号:US10871732

    申请日:2004-06-18

    CPC分类号: C07D487/04

    摘要: This invention generally relates to pyrazolo pyrimidine derivatives useful as inhibitors of short chain dehydrogenase/reductase (SDR) family of NAD(P)(H) dependent oxido-reductases. The invention further relates to pharmaceutical compositions and methods of preventing or treating disease with 1H-Pyrrolo[2.3-d]pyrimidine derivatives. More specifically, the invention relates to a 1H-Pyrrolo[2.3-d]pyrimidine which is a compound of Formula I or II: or a pharmaceutically-acceptable salt or prodrug thereof; wherein: Y is N or CR5; Z is NR3R4, halo, H, OH, alkyl, alkyloxy, or haloalkyl; and R1a is indolyl, thiazolyl, benzyl, biphenylyl, thiophenyl, pyrrolyl, or phenyl, wherein said phenyl is substituted with at least one of OH, —NR3R4, —C(═O)NR6R7, —CN, NO2—C(═O)OH, —C(═O)O-alkyl, (C1-C4)alkyl, halo, haloalkyl or haloaryl; and wherein said indolyl, thiazolyl, benzyl, biphenylyl, thiophenyl, or pyrrolyl is optionally substituted with OH, —NR3R4, —C(═O)NR6R7, —CN, NO2, —C(═O)O—R3, (C1-C4)alkyl, halo, haloalkyl or haloaryl.

    摘要翻译: 本发明一般涉及可用作NAD(P)(H)依赖性氧化还原酶的短链脱氢酶/还原酶(SDR)家族的抑制剂的吡唑并嘧啶衍生物。 本发明还涉及用1H-吡咯并[2,3-d]嘧啶衍生物预防或治疗疾病的药物组合物和方法。 更具体地,本发明涉及作为式I或II化合物的1H-吡咯并[2,3-d]嘧啶或其药学上可接受的盐或前药; 其中:Y是N或CR 5; Z是NR 3 R 4,卤素,H,OH,烷基,烷氧基或卤代烷基; 并且R 1a是吲哚基,噻唑基,苄基,联苯基,噻吩基,吡咯基或苯基,其中所述苯基被OH,-NR 3 R 3中的至少一个取代, -C(-O)NR 6 R 7,-CN,NO 2 -C(-O(O) )OH,-C(-O)O-烷基,(C 1 -C 4 -C 4)烷基,卤素,卤代烷基或卤代芳基; 并且其中所述吲哚基,噻唑基,苄基,联苯基,噻吩基或吡咯基任选被OH,-NR 3 R 4,-C( - )NR -C(O)OR 3,-C(-O)OR 3,(C 1 -C 6) C 1 -C 4烷基,卤素,卤代烷基或卤代芳基。

    Hand stand
    10.
    外观设计

    公开(公告)号:USD968138S1

    公开(公告)日:2022-11-01

    申请号:US29832941

    申请日:2022-03-31

    申请人: Chao Zhang

    设计人: Chao Zhang