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Development of Inhibitors of Protein-protein Interactions through REPLACE: Application to the Design and Development Non-ATP Competitive CDK Inhibitors
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Innovative discovery and mechanistic validation of HyT-PD ligands for selective CDK9-targeted protein degradation

Yizhan Zhai1, Jianfeng Cai1

  • 1Department of Chemistry, University of South Florida, Tampa, FL 33620, United States.

Acta Pharmaceutica Sinica. B
|June 9, 2025
PubMed
Abstract

No abstract available in PubMed .

Keywords:
ATG101Autophagy–lysosome pathwayCDK9HyT-PDsTargeted protein degrader

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The orderly progression of the cell cycle depends on the activation of Cdk protein by binding to its cyclin partner. However, the cell cycle must be restricted when undergoing abnormal changes. Most cancers correlate to the deregulated cell cycle, and since Cdks are a central component of the cell cycle, Cdk inhibitors are extensively studied to develop anticancer agents. For instance, cyclin D associates with several Cdks, such as Cdk 4/6, to form an active complex. The cyclin D-Cdk4/6 complex...
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