The SAR of 4-substituted (6,6-bicyclic) piperidine cathepsin S inhibitors

Bioorg Med Chem Lett. 2006 Apr 15;16(8):2209-12. doi: 10.1016/j.bmcl.2006.01.038. Epub 2006 Feb 3.

Abstract

A series of competitive, reversible cathepsin S (CatS) inhibitors was investigated. An earlier disclosure detailed the discovery of the 4-(2-keto-1-benzimidazolinyl)-piperidin-1-yl moiety as an effective replacement for the 4-arylpiperazin-1-yl group found in our screening hit. Continued investigation into replacements for the 4-aryl piperazine resulted in the identification of potentially useful CatS inhibitors with enzymatic and cellular activity similar to that of JNJ 10329670 as disclosed in a previous publication.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Binding Sites
  • Bridged Bicyclo Compounds / chemistry*
  • Bridged Bicyclo Compounds / pharmacology
  • Cathepsins / antagonists & inhibitors*
  • Cell Line, Tumor
  • Enzyme Inhibitors / chemistry*
  • Enzyme Inhibitors / pharmacology
  • Mice
  • Piperidines / chemistry*
  • Piperidines / pharmacology
  • Structure-Activity Relationship

Substances

  • Bridged Bicyclo Compounds
  • Enzyme Inhibitors
  • Piperidines
  • piperidine
  • Cathepsins
  • cathepsin S