Synthesis and structure activity relationships of novel small molecule cathepsin D inhibitors

Bioorg Med Chem Lett. 1999 Sep 6;9(17):2531-6. doi: 10.1016/s0960-894x(99)00433-3.

Abstract

Cathepsin D, a lysosomal aspartyl protease, has been implicated in the pathology of Alzheimer's disease as well as breast and ovarian cancer. A weakly active cathepsin D inhibitor was identified by high throughput screening. Subsequent optimization led to the discovery of a new class of small molecule inhibitors of this enzyme, culminating with the sulfonamide 13 (IC50 = 250 nM).

MeSH terms

  • Cathepsin D / antagonists & inhibitors*
  • Humans
  • Liver / enzymology
  • Protease Inhibitors / chemical synthesis*
  • Protease Inhibitors / chemistry
  • Protease Inhibitors / pharmacology
  • Structure-Activity Relationship

Substances

  • Protease Inhibitors
  • Cathepsin D