Repurposing of Human Kinase Inhibitors in Neglected Protozoan Diseases

ChemMedChem. 2017 Aug 22;12(16):1235-1253. doi: 10.1002/cmdc.201700259. Epub 2017 Jul 11.

Abstract

Human African trypanosomiasis (HAT), Chagas disease, and leishmaniasis belong to a group of infectious diseases known as neglected tropical diseases and are induced by infection with protozoan parasites named trypanosomatids. Drugs in current use have several limitations, and therefore new candidate drugs are required. The majority of current therapeutic trypanosomatid targets are enzymes or cell-surface receptors. Among these, eukaryotic protein kinases are a major group of protein targets whose modulation may be beneficial for the treatment of neglected tropical protozoan diseases. This review summarizes the finding of new hit compounds for neglected tropical protozoan diseases, by repurposing known human kinase inhibitors on trypanosomatids. Kinase inhibitors are grouped by human kinase family and discussed according to the screening (target-based or phenotypic) reported for these compounds on trypanosomatids. This collection aims to provide insight into repurposed human kinase inhibitors and their importance in the development of new chemical entities with potential beneficial effects on the diseases caused by trypanosomatids.

Keywords: drug discovery; kinase inhibitors; neglected tropical diseases; parasites; repurposing.

Publication types

  • Review

MeSH terms

  • Drug Repositioning*
  • Humans
  • Neglected Diseases / drug therapy*
  • Neglected Diseases / prevention & control
  • Protein Kinase Inhibitors / chemistry
  • Protein Kinase Inhibitors / therapeutic use*
  • Protein Serine-Threonine Kinases / antagonists & inhibitors*
  • Protein Serine-Threonine Kinases / metabolism
  • Protozoan Infections / drug therapy*
  • Protozoan Infections / prevention & control
  • Protozoan Vaccines / immunology

Substances

  • Protein Kinase Inhibitors
  • Protozoan Vaccines
  • Protein Serine-Threonine Kinases