New Therapeutic Targets for Brain Function and Disease

J Med Chem. 2020 Jun 25;63(12):6474-6476. doi: 10.1021/acs.jmedchem.9b01947. Epub 2019 Dec 17.

Abstract

Cytochrome P450 46A1 (CYP46A1) or cholesterol-24-hydroxylase is responsible for cholesterol metabolism and homeostasis in the human brain. More recently its activity has been linked to brain function and disease. The anti-HIV drug efavirenz activates CYP46A1 at low drug levels while inhibiting the enzyme activity at the high dose used in clinical practice. Synthetic analogs and hydroxylated metabolites of efavirenz enhance CYP46A1 activity, with reduced unwanted enzyme inhibition at higher concentrations. These observations provide a platform for structural modifications of efavirenz to modulate CYP46A1 activity as a therapeutic target of brain disorders such as Alzheimer's disease, for which currently no treatment is available.

Publication types

  • Editorial

MeSH terms

  • Alkynes
  • Alzheimer Disease / drug therapy*
  • Alzheimer Disease / pathology
  • Animals
  • Benzoxazines / chemistry
  • Benzoxazines / therapeutic use*
  • Brain / drug effects*
  • Cholesterol 24-Hydroxylase / chemistry
  • Cholesterol 24-Hydroxylase / metabolism*
  • Cyclopropanes
  • Cytochrome P-450 CYP3A Inducers / chemistry
  • Cytochrome P-450 CYP3A Inducers / therapeutic use*
  • Humans

Substances

  • Alkynes
  • Benzoxazines
  • Cyclopropanes
  • Cytochrome P-450 CYP3A Inducers
  • Cholesterol 24-Hydroxylase
  • efavirenz