A refined 3-dimensional QSAR of cytochrome P450 2C9: computational predictions of drug interactions

J Med Chem. 2000 Jul 27;43(15):2789-96. doi: 10.1021/jm000048n.

Abstract

A ligand-based model is reported that predicts the Ki values for cytochrome P450 2C9 (CYP2C9) inhibitors. This CoMFA model was used to predict the affinity of 14 structurally diverse compounds not in the training set and appears to be robust. The mean error of the predictions is 6 microM. The experimentally measured Ki values of the 14 compounds range from 0.1 to 48 microM. Leave-one-out cross-validated partial least-squares gives a q2 value of between 0.6 and 0.8 for the various models which indicates internal consistency. Random assignment of biological data to structure leads to negative q2 values. These models are useful in that they establish a pharmacophore for binding to CYP2C9 that can be tested with site-directed mutagenesis. These models can also be used to screen for potential drug interactions and to design compounds that will not bind to this enzyme with high affinity.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aryl Hydrocarbon Hydroxylases*
  • Binding Sites
  • Cytochrome P-450 Enzyme System / chemistry*
  • Cytochrome P-450 Enzyme System / metabolism
  • Drug Interactions
  • Enzyme Inhibitors / chemistry*
  • Ligands
  • Models, Biological
  • Models, Molecular
  • Protein Binding
  • Reproducibility of Results
  • Steroid 16-alpha-Hydroxylase*
  • Steroid Hydroxylases / chemistry*
  • Steroid Hydroxylases / metabolism
  • Structure-Activity Relationship
  • Sulfaphenazole / chemistry
  • Sulfaphenazole / metabolism
  • Sulfonamides / chemistry
  • Sulfonamides / metabolism
  • Warfarin / chemistry
  • Warfarin / metabolism

Substances

  • Enzyme Inhibitors
  • Ligands
  • Sulfonamides
  • Sulfaphenazole
  • Warfarin
  • Cytochrome P-450 Enzyme System
  • Steroid Hydroxylases
  • Aryl Hydrocarbon Hydroxylases
  • Steroid 16-alpha-Hydroxylase