Evolution of PI3Kγ and δ Inhibitors for Inflammatory and Autoimmune Diseases

被引:72
|
作者
Perry, Matthew W. D. [1 ]
Abdulai, Raolat [5 ,6 ,7 ]
Mogemark, Mickael [2 ]
Petersen, Jens [4 ]
Thomas, Matthew J. [1 ,8 ]
Valastro, Barbara [3 ]
Eriksson, Annika Westin [2 ]
机构
[1] AstraZeneca Gothenburg, Resp Inflammat & Autoimmun, SE-43183 Molndal, Sweden
[2] AstraZeneca Gothenburg, Drug Safety & Metab, SE-43183 Molndal, Sweden
[3] AstraZeneca Gothenburg, Early Clin Dev, Resp Inflammat & Autoimmun Translat Med Unit, SE-43183 Molndal, Sweden
[4] AstraZeneca Gothenburg, IMED Biotech Unit, Discovery Sci, SE-43183 Molndal, Sweden
[5] AstraZeneca, Resp Inflammat & Autoimmun Translat Med Unit, Early Clin Dev, IMED Biotech Unit, Boston, MA 02451 USA
[6] Brigham & Womens Hosp, 75 Francis St, Boston, MA 02115 USA
[7] Sanofi US, 640 Mem Dr, Cambridge, MA 02139 USA
[8] Boehringer Ingelheim Pharma GmbH & Co KG, Dept Immunol & Resp Dis Res Germany, Birkendorfer Str 65, D-88397 Biberach, Germany
关键词
PHOSPHOINOSITIDE 3-KINASE GAMMA; SELECTIVE PI3K-DELTA INHIBITOR; CHRONIC LYMPHOCYTIC-LEUKEMIA; HIGHLY POTENT; EMBRYONIC LETHALITY; ISOFORM SELECTIVITY; DISCOVERY; PI3K; IDELALISIB; KINASE;
D O I
10.1021/acs.jmedchem.8b01298
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Phosphoinositol 3-kinases (PI3Ks) gamma and delta are key enzymes in hematopoietic cells and have been seen as high-value targets for the treatment of diseases with inflammatory and immunomodulatory components since their discovery and the identification of their roles. In this Perspective we review progress in the application of inhibitors of PI3K gamma and delta to inflammatory and immunological conditions over the past 6 years. We consider progress in the understanding of the roles of PI3K gamma and PI3K delta in immunology and inflammation, the experience from clinical trials where inhibitors have been tested, and what has been learned about the safety of their use. The extensive medicinal chemistry efforts to discover both isoform selective and dual PI3K gamma delta inhibitors are analyzed and detailed. Developments in understanding the structural chemistry of the PI3K enzymes and the factors that govern isoform selectivity are discussed. The effects observed with the known inhibitor compounds in animal models are described.
引用
收藏
页码:4783 / 4814
页数:32
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