Advances in synthesis and biological evaluation of CDK2 inhibitors for cancer therapy

Bioorg Chem. 2024 Feb:143:107045. doi: 10.1016/j.bioorg.2023.107045. Epub 2023 Dec 21.

Abstract

One of the leading causes of mortality in the world is cancer. This disease occurs when responsible genes that regulate the cell cycle become inactive due to internal or external factors. Specifically, the G1/S and S/G2 transitions in the cell cycle are controlled by a protein called cyclin-dependent kinase 2 (CDK2). CDKs, which play a crucial role in managing the cell cycle, have been a wide area of research in cancer treatment. Over the past 11 years, significant research has been made in identifying potent, targeted, and efficient inhibitors of CDK2. In this summary, we have summarized recent developments in the synthesis and biological evaluation of CDK2 inhibitors.

Keywords: Anticancer; Antiproliferative activity; CDK2 enzyme; CDK2 inhibitor; Cell cycle arrest.

Publication types

  • Review

MeSH terms

  • CDC2-CDC28 Kinases*
  • Cell Cycle
  • Cell Cycle Proteins
  • Cyclin-Dependent Kinase 2
  • Cyclin-Dependent Kinases
  • Enzyme Inhibitors / pharmacology
  • Neoplasms* / drug therapy
  • Protein Serine-Threonine Kinases

Substances

  • Cyclin-Dependent Kinase 2
  • Protein Serine-Threonine Kinases
  • CDC2-CDC28 Kinases
  • Cyclin-Dependent Kinases
  • Cell Cycle Proteins
  • Enzyme Inhibitors