단백질 키나아제 저해활성을 가지는 2,4,7-치환된 티에노[3,2-d]피리미딘 화합물
    11.
    发明公开
    단백질 키나아제 저해활성을 가지는 2,4,7-치환된 티에노[3,2-d]피리미딘 화합물 有权
    作为蛋白激酶抑制剂的2,4,7-取代的三[3,2-D]吡啶化合物

    公开(公告)号:KR1020110055202A

    公开(公告)日:2011-05-25

    申请号:KR1020090112132

    申请日:2009-11-19

    CPC classification number: C07D495/04

    Abstract: PURPOSE: A 2,4,7-substituted thieno[3,2-d]pyrimidine compound is provided to inhibit protein kinase activity and to prevent abnormal cell proliferation-induced diseases. CONSTITUTION: A 2,4,7-substituted thieno[3,2-d]pyrimidine compound with an activity of suppressing protein kinase, isomer, pharmaceutically acceptable salt, hydrate, or solvate thereof is denoted by chemical formula 1. In chemical formula 1, A is hydroxy C1-C6 alkyl group, phenyl group, or hetero aryl group containing 1-3 nitrogen atoms; and Ra is hydrogen atom, C1-C6 alkyl group, C1-C6 alkoxy group, or heterocycloalkyl group containing 1-3 hetero atoms selected from oxygen and nitrogen.

    Abstract translation: 目的:提供2,4,7-取代的噻吩并[3,2-d]嘧啶化合物以抑制蛋白激酶活性并防止异常细胞增殖诱导的疾病。 构成:具有抑制蛋白激酶,异构体,药学上可接受的盐,水合物或溶剂合物的活性的2,4,7-取代的噻吩并[3,2-d]嘧啶化合物由化学式1表示。在化学式1中 A是羟基C1-C6烷基,苯基或含1-3个氮原子的杂芳基; 并且R a是氢原子,C 1 -C 6烷基,C 1 -C 6烷氧基或含1-3个选自氧和氮的杂原子的杂环烷基。

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