Multiple strategies for the preparation of a sulfur-35 labeled NPC1L1 radioligand

Bioorg Med Chem Lett. 2009 Sep 1;19(17):5033-6. doi: 10.1016/j.bmcl.2009.07.051. Epub 2009 Jul 22.

Abstract

During our effort to design a receptor binding assay to aid in the elucidation of the molecular mechanism of ezetimibe, we prepared a sulfur-35 containing radioligand which exhibits improved potency over the glucuronide conjugate of ezetimibe in both native enterocyte brush border membranes and membranes from cells expressing recombinant NPC1L1. Herein, we describe the different synthetic strategies which were used to obtain this compound as well as its effectiveness in the aforementioned assay.

MeSH terms

  • Animals
  • Anticholesteremic Agents / chemical synthesis
  • Anticholesteremic Agents / chemistry*
  • Anticholesteremic Agents / pharmacology
  • Azetidines / chemical synthesis
  • Azetidines / chemistry*
  • Azetidines / pharmacology
  • Cell Line
  • Ezetimibe
  • Glucuronides / chemistry
  • Humans
  • Ligands
  • Membrane Proteins / antagonists & inhibitors*
  • Membrane Proteins / metabolism
  • Membrane Transport Proteins
  • Mice
  • Protein Binding
  • Rats
  • Recombinant Proteins / antagonists & inhibitors
  • Recombinant Proteins / metabolism
  • Sulfur Radioisotopes / chemistry

Substances

  • Anticholesteremic Agents
  • Azetidines
  • Glucuronides
  • Ligands
  • Membrane Proteins
  • Membrane Transport Proteins
  • NPC1L1 protein, human
  • Recombinant Proteins
  • Sulfur Radioisotopes
  • Ezetimibe