Discovery of vimseltinib (DCC-3014), a highly selective CSF1R switch-control kinase inhibitor, in clinical development for the treatment of Tenosynovial Giant Cell Tumor (TGCT)

Bioorg Med Chem Lett. 2022 Oct 15:74:128928. doi: 10.1016/j.bmcl.2022.128928. Epub 2022 Aug 10.

Abstract

Based on knowledge of kinase switch-control inhibition and using a combination of structure-based drug design and standard medicinal chemistry principles, we identified a novel series of dihydropyrimidone-based CSF1R kinase inhibitors displaying exquisite selectivity for CSF1R versus a large panel of kinases and non-kinase protein targets. Starting with lead compound 3, an SAR optimization campaign led to the discovery of vimseltinib (DCC-3014; compound 20) currently undergoing clinical evaluation for the treatment of Tenosynovial Giant Cell Tumor (TGCT), a locally aggressive benign tumor associated with substantial morbidity. 2021 Elsevier ltd. All rights reserved.

Keywords: CSF1R; Cancer; Kinase; Switch-control; TGCT.

MeSH terms

  • Antineoplastic Agents* / pharmacology
  • Antineoplastic Agents* / therapeutic use
  • DCC Receptor
  • Giant Cell Tumor of Tendon Sheath* / drug therapy
  • Giant Cell Tumor of Tendon Sheath* / pathology
  • Humans
  • Protein Kinase Inhibitors / pharmacology
  • Protein Kinase Inhibitors / therapeutic use
  • Receptor Protein-Tyrosine Kinases
  • Receptor, Macrophage Colony-Stimulating Factor

Substances

  • Antineoplastic Agents
  • DCC Receptor
  • DCC protein, human
  • Protein Kinase Inhibitors
  • Receptor Protein-Tyrosine Kinases
  • Receptor, Macrophage Colony-Stimulating Factor