Tiratricol, a thyroid hormone metabolite, has potent inhibitory activity against human dihydroorotate dehydrogenase

Chem Biol Drug Des. 2023 Jul;102(1):1-13. doi: 10.1111/cbdd.14256. Epub 2023 Apr 23.

Abstract

Human dihydroorotate dehydrogenase (hDHODH) is a promising drug target for many diseases including autoimmune diseases, cancer, and viral infection. To develop more novel and potent hDHODH inhibitors, we screened our in-house library of old drugs. We found that tiratricol (3,3',5-triiodothyroacetic acid), a thyroid hormone metabolite, has potent hDHODH inhibitory activity (IC50 : 0.754 ± 0.126 μM), and its precursor tetrac (3,3',5,5'-tetraiodothyroacetic acid) also shows a certain inhibitory activity against hDHODH (IC50 : 11.960 ± 1.453 μM). Enzyme kinetic analysis shows that tiratricol and tetrac are noncompetitive inhibitors versus CoQ0 , which is different from the positive control A771726. ThermoFMN assay, molecular docking and site-directed mutagenesis all indicate that tiratricol and tetrac interact with more key residues of hDHODH than A771726, especially some hydrophobic residues in Subsite 1. In conclusion, our experiment results indicate a potential new use for the old drug, tiratricol, and provide a novel chemical scaffold for the design of hDHODH inhibitors.

Keywords: ThermoFMN assay; human dihydroorotate dehydrogenase; molecular docking; site-directed mutagenesis; tiratricol.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Dihydroorotate Dehydrogenase*
  • Enzyme Inhibitors / chemistry
  • Humans
  • Kinetics
  • Molecular Docking Simulation
  • Oxidoreductases Acting on CH-CH Group Donors*
  • Structure-Activity Relationship
  • Thyroid Hormones

Substances

  • 3,3',5-triiodothyroacetic acid
  • Dihydroorotate Dehydrogenase
  • Enzyme Inhibitors
  • Oxidoreductases Acting on CH-CH Group Donors
  • teriflunomide
  • Thyroid Hormones
  • tetraiodothyroacetic acid