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A patent review of anticancer CDK2 inhibitors (2017-present)
被引:13
|作者:
Said, Mohamed A.
[1
]
Abdelrahman, Mohamed A.
[1
]
Abourehab, Mohammed A. S.
[3
,4
]
Fares, Mohamed
[1
,2
]
Eldehna, Wagdy M.
[5
,6
]
机构:
[1] Egyptian Russian Univ, Dept Pharmaceut Chem, Fac Pharm, Cairo, Egypt
[2] Univ Sydney, Sch Chem, Sydney, NSW, Australia
[3] Umm Al Qura Univ, Dept Pharmaceut, Fac Pharm, Mecca, Saudi Arabia
[4] Minia Univ, Dept Pharmaceut & Ind Pharm, Fac Pharm, Al Minya, Egypt
[5] Badr Univ Cairo, Sch Biotechnol, Cairo 11829, Egypt
[6] Kafrelsheikh Univ, Dept Pharmaceut Chem, Fac Pharm, Kafrelsheikh, Egypt
关键词:
Anticancer;
CDK inhibitors;
kinase inhibitors;
cyclins;
cell cycle;
CYCLIN-DEPENDENT KINASES;
CANCER-THERAPY;
MECHANISM;
FUTURE;
D O I:
10.1080/13543776.2022.2078193
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
Introduction The success of the CDK4/6 inhibitor Ibrance (TM) (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. Areas covered 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. Expert opinion 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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页码:885 / 898
页数:14
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