Phosphatidylinositol 3-Kinase (PI3K) and Phosphatidylinositol 3-Kinase-Related Kinase (PIKK) Inhibitors: Importance of the Morpholine Ring

被引:135
作者
Andrs, Martin [1 ,2 ]
Korabecny, Jan [1 ]
Jun, Daniel [1 ,2 ]
Hodny, Zdenek [3 ]
Bartek, Jiri [3 ,4 ]
Kuca, Kamil [1 ]
机构
[1] Univ Hosp Hradec Kralove, Biomed Res Ctr, Hradec Kralove 50005, Czech Republic
[2] Univ Def, Fac Mil Hlth Sci, Dept Toxicol & Mil Pharm, Hradec Kralove 50001, Czech Republic
[3] ASCR, Vvi, Inst Mol Genet, Dept Genome Integr, Prague 14220, Czech Republic
[4] Danish Canc Soc, Res Ctr, DK-2100 Copenhagen, Denmark
关键词
DEPENDENT PROTEIN-KINASE; STRAND BREAK REPAIR; TARGETING DNA-REPAIR; IN-VIVO EVALUATION; MAMMALIAN TARGET; ATAXIA-TELANGIECTASIA; (PI3K)/MAMMALIAN TARGET; PI3K/AKT/MTOR PATHWAY; BIOLOGICAL EVALUATION; SELECTIVE INHIBITOR;
D O I
10.1021/jm501026z
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Phosphatidylinositol 3-kinases (PI3Ks) and phosphatidylinositol 3-kinase-related protein kinases (PIKKs) are two related families of kinases that play key roles in regulation of cell proliferation, metabolism, migration, survival, and responses to diverse stresses including DNA damage. To design novel efficient strategies for treatment of cancer and other diseases, these kinases have been extensively studied. Despite their different nature, these two kinase families have related origin and share very similar kinase domains. Therefore, chemical inhibitors of these kinases usually carry analogous structural motifs. The most common feature of these inhibitors is a critical hydrogen bond to morpholine oxygen, initially present in the early nonspecific PI3K and PIKK inhibitor 3 (LY294002), which served as a valuable chemical tool for development of many additional PI3K and PIKK inhibitors. While several PI3K pathway inhibitors have recently shown promising clinical responses, inhibitors of the DNA damage-related PIKKs remain thus far largely in preclinical development.
引用
收藏
页码:41 / 71
页数:31
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