REVIEW

Rencent Advances in Cyclin-Dependent Kinase Inhibitors with Purine Scaffold

  • Zhang Jingyu ,
  • Wang Qinglong ,
  • Hou Xuehui ,
  • Liu Hongmin
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  • a School of Pharmaceutical Science, Henan University of Taditional Chinese Medicine, Zhengzhou 450008;
    b Department of Quality Detection and Management, Henan University of Animal Husbandry and Economy, Zhengzhou 450011;
    c School of Pharmaceutical Science, Zhengzhou University, Zhengzhou 450001

Received date: 2014-10-29

  Revised date: 2014-11-28

  Online published: 2014-12-02

Supported by

Project supported by the Education Department of Henan Province Science and Technology Research Projects (No.14A150052), Scientific Research Plan of Zhenzhou (No.121PPTGG509-2).

Abstract

Cell cycle is a basic characteristic of a cell that associates with its division and duplication. An entire cell cycle is regulated by a series of enzymes. The occurance of cell cycle disorder can lead to an excessive cell proliferation which may trigger cancer. However, the drugs that target cyclin-dependent kinases could spur the process of cancer cell apoptosis through interrupting the cell cycle. In this article, different kinds of cyclin-dependent kinases (CDKs), cyclins, the mechanism of cell cycle regulation and its relation with cancers are reviewed. The CDKs inhibitors with purine scaffold are introduced and their progresses in research and development are briefly discussed.

Cite this article

Zhang Jingyu , Wang Qinglong , Hou Xuehui , Liu Hongmin . Rencent Advances in Cyclin-Dependent Kinase Inhibitors with Purine Scaffold[J]. Chinese Journal of Organic Chemistry, 2015 , 35(5) : 1022 -1032 . DOI: 10.6023/cjoc201410039

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