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    Compounds for inhibiting AGC kinase and pharmaceutical compositions comprising the same
    2.
    发明授权
    Compounds for inhibiting AGC kinase and pharmaceutical compositions comprising the same 有权

    公开(公告)号：US10696638B2

    公开(公告)日：2020-06-30

    申请号：US16206000

    申请日：2018-11-30

    Applicant: Industrial Technology Research Institute

    Inventor： Chih-Hung Chen ,  Yi-Hsun Chen ,  Jui-Wen Huang ,  Kuo-Kuei Huang ,  Chih-Peng Liu ,  Chrong-Shiong Hwang

    IPC: C07D217/02 ,  A61K31/472 ,  A61P27/02 ,  A61K31/4725 ,  A61K9/08 ,  A61K9/00

    Abstract: A compound of formula (I) or a pharmaceutically acceptable salt thereof is provided. In formula (I), Ar is indazole, 5-isoquinoline, 6-isoquinoline, or their N-oxide. X is —C(═Z)—, wherein Z is N—CN, NH, NR4, NCOR4, NCONR4R5, NCO-aryl, S, or O. Y and J are independently H, alkyl, aryl, aminoalkyl, —NH2, —CN, —OH, —O-alkyl, —O-aryl, —COOH, —COOR4, —CONHR4, —CONHCH2-aryl, —CONR4CH2-aryl, —NHCOR4, halogen, halogened alkyl, -alkyl-OR4, -alkyl-ONO2, alkyl-ONO2, —OCOOR4, —O(C═O)-aryl, —CHR4OH, —CH2OH, —CH2O(C═O)-aryl, —CH2O(C═O)—R4, —CHR4O(C═O)-aryl, —CHR4O(C═O)—R4, unsaturated carboxylic ester, substituted alkynyl, —NHSO2R4, —SO2R4, —SO2NHR4, or —SO2NR4R5, or Y and J bond together to form a carbocylic or aromatic ring, wherein R4 and R5 are independently H, substituted C1-C6 alkyl, substituted aryl, cycloalkyl, alkylaryl, -alkyl-NR6R7, —S(O)0-2-(alkyl-NR6R7). R1, R2 and R3 are H, C1-C6 alkyl, cycloalkyl, aryl, alkylaryl, alkylheteroaryl, alkylheterocycle, wherein any one thereof is optionally substituted with one or more of OH, NO2, or NR8R9.

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