细胞周期蛋白依赖激酶
细胞周期蛋白依赖激酶2
帕博西利布
药物发现
激酶
癌症研究
生物
癌症
细胞周期
生物化学
蛋白激酶A
细胞
遗传学
乳腺癌
转移性乳腺癌
作者
Mohamed A. Said,Mohamed A. Abdelrahman,Mohammed A. S. Abourehab,Mohamed Farès,Wagdy M. Eldehna
标识
DOI:10.1080/13543776.2022.2078193
摘要
The success of the CDK4/6 inhibitor Ibrance™ (Palbociclib) as an anticancer agent inspired and directed more efforts toward the discovery of selective cyclin-dependent kinase (CDKs) inhibitors. CDK2 is a member of the CDKs family that plays an important role in regulating the progression of cells into both S- and M-phases of the cell cycle. Studies suggest that overexpression of CDK2 may be implicated in tumor growth in cancer.This review covers the patent literature of CDK2 inhibitors published between 2017 and 2021. We searched the online databases of the European Patent Office, American Chemical Society, and Google patents.Developing selective CDK2 inhibitors is challenging due to the absence of a previously approved selective CDK2 inhibitor. However, ongoing efforts by Incyte Corporation and Pfizer Inc., which are reported herein, may stand out as a new starting point and bring novel information critical for the medicinal chemistry and drug design scientists in the field of CDK2 inhibitors' development.
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