首页 | 本学科首页   官方微博 | 高级检索  
     


Development of CDK4/6 Inhibitors: A Five Years Update
Authors:Alessandra Ammazzalorso  Mariangela Agamennone  Barbara De Filippis  Marialuigia Fantacuzzi
Affiliation:Unit of Medicinal Chemistry, Department of Pharmacy, “G. d’Annunzio” University, 66100 Chieti, Italy; (A.A.); (M.A.); (B.D.F.)
Abstract:The inhibition of cyclin dependent kinases 4 and 6 plays a role in aromatase inhibitor resistant metastatic breast cancer. Three dual CDK4/6 inhibitors have been approved for the breast cancer treatment that, in combination with the endocrine therapy, dramatically improved the survival outcomes both in first and later line settings. The developments of the last five years in the search for new selective CDK4/6 inhibitors with increased selectivity, treatment efficacy, and reduced adverse effects are reviewed, considering the small-molecule inhibitors and proteolysis-targeting chimeras (PROTACs) approaches, mainly pointing at structure-activity relationships, selectivity against different kinases and antiproliferative activity.
Keywords:cyclin-dependent kinase   cancer   resistance   small molecule inhibitors   PROTACs
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号