Design, Synthesis, and Characterization of a Photoactivatable Caged Prodrug of Imatinib

ChemMedChem. 2015 Aug;10(8):1335-8. doi: 10.1002/cmdc.201500163. Epub 2015 Jun 15.

Abstract

Imatinib is the first protein kinase inhibitor approved for clinical use and is a seminal drug for the concept of targeted therapy. Herein we report on the design, synthesis, photokinetic properties, and in vitro enzymatic evaluation of a photoactivatable caged prodrug of imatinib. This approach allows spatial and temporal control over the activation of imatinib triggered by ultraviolet light. The successful application of the photoactivation concept to this significant kinase inhibitor provides further evidence for the caging technique as a feasible approach in the kinase field. The presented photoactivatable imatinib prodrug will be highly useful as a pharmacological tool to study the impact of imatinib toward biological systems in greater detail.

Keywords: PDGF-Rβ; caged prodrugs; imatinib; inhibitors; kinases; photoactivation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Catalytic Domain
  • Drug Design*
  • Imatinib Mesylate / chemical synthesis
  • Imatinib Mesylate / chemistry*
  • Molecular Docking Simulation
  • Prodrugs / chemical synthesis
  • Prodrugs / chemistry*
  • Protein Kinase Inhibitors / chemical synthesis*
  • Protein Kinase Inhibitors / chemistry
  • Receptor, Platelet-Derived Growth Factor beta / chemistry
  • Receptor, Platelet-Derived Growth Factor beta / metabolism
  • Ultraviolet Rays

Substances

  • Prodrugs
  • Protein Kinase Inhibitors
  • Imatinib Mesylate
  • Receptor, Platelet-Derived Growth Factor beta