Repositioning organohalogen drugs: a case study for identification of potent B-Raf V600E inhibitors via docking and bioassay

Sci Rep. 2016 Aug 9:6:31074. doi: 10.1038/srep31074.

Abstract

Drug repositioning has been attracting increasingly attention for its advantages of reducing costs and risks. Statistics showed that around one quarter of the marketed drugs are organohalogens. However, no study has been reported, to the best of our knowledge, to aim at efficiently repositioning organohalogen drugs, which may be attributed to the lack of accurate halogen bonding scoring function. Here, we present a study to show that two organohalogen drugs were successfully repositioned as potent B-Raf V600E inhibitors via molecular docking with halogen bonding scoring function, namely D(3)DOCKxb developed in our lab, and bioassay. After virtual screening by D(3)DOCKxb against the database CMC (Comprehensive Medicinal Chemistry), 3 organohalogen drugs that were predicted to form strong halogen bonding with B-Raf V600E were purchased and tested with ELISA-based assay. In the end, 2 of them, rafoxanide and closantel, were identified as potent inhibitors with IC50 values of 0.07 μM and 1.90 μM, respectively, which are comparable to that of vemurafenib (IC50: 0.17 μM), a marketed drug targeting B-Raf V600E. Single point mutagenesis experiments confirmed the conformations predicted by D(3)DOCKxb. And comparison experiment revealed that halogen bonding scoring function is essential for repositioning those drugs with heavy halogen atoms in their molecular structures.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution
  • Drug Evaluation, Preclinical
  • Drug Repositioning*
  • Halogens / chemistry
  • Halogens / pharmacokinetics
  • Halogens / pharmacology
  • Humans
  • In Vitro Techniques
  • Molecular Docking Simulation
  • Molecular Structure
  • Mutagenesis, Site-Directed
  • Organic Chemicals / chemistry
  • Organic Chemicals / pharmacokinetics
  • Organic Chemicals / pharmacology
  • Protein Kinase Inhibitors / chemistry
  • Protein Kinase Inhibitors / pharmacokinetics
  • Protein Kinase Inhibitors / pharmacology*
  • Proto-Oncogene Proteins B-raf / antagonists & inhibitors*
  • Proto-Oncogene Proteins B-raf / genetics
  • Proto-Oncogene Proteins B-raf / metabolism
  • Rafoxanide / chemistry
  • Rafoxanide / pharmacokinetics
  • Rafoxanide / pharmacology
  • Salicylanilides / chemistry
  • Salicylanilides / pharmacokinetics
  • Salicylanilides / pharmacology
  • User-Computer Interface

Substances

  • Halogens
  • Organic Chemicals
  • Protein Kinase Inhibitors
  • Salicylanilides
  • Rafoxanide
  • BRAF protein, human
  • Proto-Oncogene Proteins B-raf
  • closantel