Cyclin-dependent kinase 4 inhibitors as a treatment for cancer. Part 1: identification and optimisation of substituted 4,6-Bis anilino pyrimidines

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High-Resolution Crystal Structures of Human Cyclin-Dependent Kinase 2 with and without ATP:  Bound Waters and Natural Ligand as Guides for Inhibitor Design

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Structure-Based Generation of a New Class of Potent Cdk4 Inhibitors:  New<i>de Novo</i>Design Strategy and Library Design

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Drug Target, Biomolecular Structure Prediction, Molecular Biology +22

Inhibition of Cyclin-Dependent Kinase 4 (Cdk4) by Fascaplysin, a Marine Natural Product

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Marine Biotechnology, Engineering, Biochemistry +7