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CDK-b is a preclinical-stage small molecule program developed by PRISM BioLab for the treatment of oncology. The program utilizes PRISM's proprietary PepMetics technology, which involves the design of small molecules that mimic the alpha-helix or beta-turn structures of proteins to modulate protein-protein interactions (PPIs). CDK-b is specifically designed to inhibit the interaction between a cyclin-dependent kinase (CDK) and its regulatory cyclin subunit. By disrupting this PPI, the drug aims to inhibit the enzymatic activity of the CDK/Cyclin complex, thereby blocking cell cycle progression in malignant cells. The program is currently in the hit identification phase of development.
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