Chemoinformatic characterization of activity and selectivity switches of antiprotozoal compounds

Future Med Chem. 2014 Mar;6(3):281-94. doi: 10.4155/fmc.13.173. Epub 2013 Nov 27.

Abstract

Background: Benzimidazole derivatives are promising compounds for the treatment of parasitic infections. The structure-activity relationships of 91 benzimidazoles with activity against Trichomonas vaginalis and Giardia intestinalis were analyzed using a novel activity landscape modeling approach.

Results: We identified two prominent cases of 'activity switches' and 'selectivity switches' where two R group substitutions in the benzimidazole scaffold completely invert the activity and selectivity pattern for T. vaginalis and G. intestinalis.

Conclusion: A chemoinformatic methodology was used to rapidly identify discrete structural changes around the central scaffold that are associated with large changes in biological activity for each parasite. The structure-activity relationships for the benzimidazole derivatives is smooth for both protozoan with few but markedly important activity cliffs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antiprotozoal Agents / chemistry*
  • Antiprotozoal Agents / pharmacology
  • Benzimidazoles / chemistry*
  • Benzimidazoles / pharmacology
  • Computer-Aided Design
  • Databases, Pharmaceutical
  • Drug Design
  • Female
  • Giardia lamblia / drug effects*
  • Giardiasis / drug therapy*
  • Humans
  • Structure-Activity Relationship
  • Trichomonas Vaginitis / drug therapy*
  • Trichomonas vaginalis / drug effects*

Substances

  • Antiprotozoal Agents
  • Benzimidazoles
  • benzimidazole