Skip to content
2000
Volume 15, Issue 10
  • ISSN: 1568-0266
  • E-ISSN: 1873-4294

Abstract

Mutations in the gene for leucine-rich repeat kinase 2 (LRRK2) have been linked to several familial and sporadic late-onset cases of Parkinson’s disease. The cumulative data for the effects of mutant forms of this enzyme on neuronal degradation and the pathophysiology of Parkinson’s disease create a compelling case for drug discovery based on inhibition of the mutant forms of LRRK2. This review focuses on structure-activity relationships for inhibitors of LRRK2 and the data supporting a potential role of these agents in treating Parkinson’s disease.

Loading

Article metrics loading...

/content/journals/ctmc/10.2174/156802661510150328223655
2015-05-01
2025-06-17
Loading full text...

Full text loading...

/content/journals/ctmc/10.2174/156802661510150328223655
Loading
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test