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Ebvaciclib (PF-06873600) is an orally bioavailable, small molecule inhibitor of cyclin-dependent kinase 2, 4, and 6 (CDK2/4/6), developed for the treatment of cancer. By selectively targeting and inhibiting these CDKs, ebvaciclib disrupts cell cycle progression—leading to cell cycle arrest, induction of apoptosis, and inhibition of tumor cell proliferation. CDKs are ATP-dependent serine/threonine kinases that regulate the cell cycle and are often overexpressed in tumor cells. Ebvaciclib has shown potential antineoplastic activity in preclinical models and is being investigated in clinical trials for various cancers[1][3][5][7].
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