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

[Display omitted] 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 call...

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Veröffentlicht in:Bioorganic chemistry 2024-02, Vol.143, p.107045-107045, Article 107045
Hauptverfasser: Patel, Dharmesh A., Patel, Siddharth S., Patel, Hitesh D.
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Sprache:eng
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Zusammenfassung:[Display omitted] 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.
ISSN:0045-2068
1090-2120
DOI:10.1016/j.bioorg.2023.107045