Skip to main navigation Skip to search Skip to main content

Kinase targets in CNS drug discovery

  • Hendra Gunosewoyo*
  • , Lifang Yu
  • , Lenka Munoz
  • , Michael Kassiou
  • *Corresponding author for this work
  • Curtin University
  • University of Sydney

Research output: Contribution to journalArticlepeer-review

Abstract

Originally thought to be nondruggable, kinases represent attractive drug targets for pharmaceutical companies and academia. To date, there are over 40 kinase inhibitors approved by the US FDA, with 32 of these being small molecules, in addition to the three mammalian target of rapamycin inhibitor macrolides (sirolimus, temsirolimus and everolimus). Despite the rapid development of kinase inhibitors for cancer, presently none of these agents are approved for CNS indications. This mini perspective highlights selected kinase targets for CNS disorders, of which brain-permeable small-molecule inhibitors are reported, with demonstrated preclinical proof-of-concept efficacy. This is followed by a brief discussion on the key challenges of blood-brain barrier penetration and selectivity profiles in developing kinase inhibitors for CNS disorders.

Original languageEnglish
Pages (from-to)303-314
Number of pages12
JournalFuture Medicinal Chemistry
Volume9
Issue number3
DOIs
StatePublished - Mar 2017

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • GSK-3
  • LRRK2
  • blood-brain barrier
  • brain cancer
  • dual-specificity kinase inhibitors
  • kinase
  • neurodegenerative diseases

Fingerprint

Dive into the research topics of 'Kinase targets in CNS drug discovery'. Together they form a unique fingerprint.

Cite this