Evaluation of structurally diverse neuronal nicotinic receptor ligands for selectivity at the alpha6( *) subtype

Bioorg Med Chem Lett. 2009 Aug 1;19(15):4359-63. doi: 10.1016/j.bmcl.2009.05.085. Epub 2009 May 27.

Abstract

Direct comparison of pyridine versus pyrimidine substituents on a small but diverse set of ligands indicates that the pyrimidine substitution has the potential to enhance affinity and/or functional activity at alpha6 subunit-containing neuronal nicotinic receptors (NNRs) and decrease activation of ganglionic nicotinic receptors, depending on the scaffold. The ramifications of this structure-activity relationship are discussed in the context of the design of small molecules targeting smoking cessation.

Publication types

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

MeSH terms

  • Animals
  • Chemistry, Pharmaceutical / methods*
  • Dopamine / metabolism
  • Drug Design
  • Humans
  • Kinetics
  • Ligands
  • Mice
  • Models, Chemical
  • Nicotine / chemistry
  • Parkinson Disease / drug therapy
  • Protein Binding
  • Pyrimidines / chemistry
  • Receptors, Nicotinic / chemistry*
  • Smoking Cessation / methods*
  • Structure-Activity Relationship

Substances

  • CHRNA6 protein, human
  • Ligands
  • Pyrimidines
  • Receptors, Nicotinic
  • Nicotine
  • Dopamine