Human acidic mammalian chitinase as a novel target for anti-asthma drug design using in silico screening

Bioorg Med Chem. 2013 Jun 1;21(11):3214-20. doi: 10.1016/j.bmc.2013.03.047. Epub 2013 Apr 1.

Abstract

Human acidic mammalian chitinase (hAMCase) was recently shown to be involved in the development of asthma, suggesting a possible application for hAMCase inhibitors as novel therapeutic agents for asthma. We therefore initiated drug discovery research into hAMCase using a combination of in silico methodologies and a hAMCase assay system. We first selected 23 candidate hAMCase inhibitors from a database of four million compounds using a multistep screening system combining Tripos Topomer Search technology, a docking calculation and two-dimensional molecular similarity analysis. We then measured hAMCase inhibitory activity of the selected compounds and identified seven compounds with IC50 values ≤100 μM. A model describing the binding modes of these hit compounds to hAMCase was constructed, and we discuss the structure-activity relationships of the compounds we identified, suggested by the model and the actual inhibitory activities of the compounds.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Asthmatic Agents / chemistry*
  • Binding Sites
  • Chitinases / antagonists & inhibitors*
  • Chitinases / chemistry
  • Computer Simulation
  • Databases, Chemical
  • Drug Design
  • High-Throughput Screening Assays
  • Humans
  • Molecular Docking Simulation*
  • Peptides, Cyclic / chemistry*
  • Protein Binding
  • Recombinant Proteins / chemistry
  • Structure-Activity Relationship

Substances

  • Anti-Asthmatic Agents
  • Peptides, Cyclic
  • Recombinant Proteins
  • argifin
  • CHIA protein, human
  • Chitinases