Synthesis and biological evaluation of 3-alkyl-dihydrotetrabenazine derivatives as vesicular monoamine transporter-2 (VMAT2) ligands

Bioorg Med Chem Lett. 2011 Jun 1;21(11):3435-8. doi: 10.1016/j.bmcl.2011.03.113. Epub 2011 Apr 5.

Abstract

In the search of new probes for in vivo brain imaging of vesicular monoamine transporter type 2 (VMAT2), we have developed an efficient synthesis of a novel series of 3-alkyl-dihydrotetrabenazine (DTBZ) derivatives. The affinity of VMAT2 was evaluated by an in vitro inhibitory binding assay using [(125)I]-iodovinyl-TBZ or [(18)F](+)-FP-DTBZ as radioligands in rat striatal tissue homogenates. New DTBZ derivatives exhibited moderate to good binding affinity to VMAT2. Among these new ligands, compound 4b showed the best affinity for VMAT2 (K(i)=5.98 nM) and may be a useful lead compound for future structure-activity studies.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Corpus Striatum / chemistry
  • Corpus Striatum / metabolism
  • Crystallography, X-Ray
  • Diagnostic Imaging
  • Fluorine Radioisotopes*
  • Ligands
  • Molecular Structure
  • Positron-Emission Tomography
  • Rats
  • Tetrabenazine / analogs & derivatives*
  • Tetrabenazine / chemical synthesis
  • Tetrabenazine / chemistry
  • Vesicular Monoamine Transport Proteins / chemistry*

Substances

  • Fluorine Radioisotopes
  • Ligands
  • Vesicular Monoamine Transport Proteins
  • dihydrotetrabenazine
  • Tetrabenazine