[EN] HETEROCYCLIC MITOCHONDRIAL ACTIVITY INHIBITORS AND USES THEREOF<br/>[FR] INHIBITEURS HÉTÉROCYCLIQUES DE L'ACTIVITÉ MITOCHONDRIALE ET UTILISATIONS ASSOCIÉES
申请人:UNIV MONTREAL
公开号:WO2019084662A1
公开(公告)日:2019-05-09
Heterocyclic compounds of Formula (I) and pharmaceutically acceptable salt thereof are disclosed. The use of such heterocyclic compounds and pharmaceutically acceptable salt thereof for the treatment of cancers, and more particularly cancers sensitive to mitochondrial activity inhibition and increased reactive oxygen species (ROS) levels, is also disclosed. Such cancers include acute myeloid leukemia (AML), preferably AML characterized by certain features, such as high level of expression of one or more Homeobox (HOX)-network genes, high and/or low expression of specific genes, the presence of one or more cytogenetic or molecular risk factors such as intermediate cytogenetic risk, Normal Karyotype (A/K), mutated NPM1, mutated CEBPA, mutated FLT3, mutated DNMT3A, mutated TET2, mutated IDH1, mutated IDH2, mutated RUNX1, mutated WT1, mutated SRSF2, intermediate cytogenetic risk with abnormal karyotype (intern(abnK)), trisomy 8 (+8) and/or abnormal chromosome (5/7), and/or a high leukemic stem cell (LSC) frequency.
化合物的分子式(I)的杂环化合物及其药用盐已被披露。还披露了这种杂环化合物及其药用盐用于治疗癌症,尤其是对于对线粒体活性抑制和增加活性氧化物(ROS)水平敏感的癌症。这些癌症包括急性髓样白血病(AML),最好是具有某些特征的AML,例如高水平表达一个或多个Homeobox(HOX)网络基因,特定基因的高和/或低表达,存在一个或多个细胞遗传学或分子风险因素,如中等细胞遗传学风险,正常核型(A/K),突变NPM1,突变CEBPA,突变FLT3,突变DNMT3A,突变TET2,突变IDH1,突变IDH2,突变RUNX1,突变WT1,突变SRSF2,具有异常核型的中等细胞遗传学风险(intern(abnK)),三体8(+8)和/或异常染色体(5/7),和/或高白血病干细胞(LSC)频率。