Solid-phase synthesis and pharmacological evaluation of analogues of PhTX-12-A potent and selective nicotinic acetylcholine receptor antagonist

Bioorg Med Chem Lett. 2002 Apr 22;12(8):1159-62. doi: 10.1016/s0960-894x(02)00120-8.

Abstract

Philanthotoxin-12 (PhTX-12) is a novel potent and selective, noncompetitive antagonist of nicotinic acetylcholine receptors (nAChRs). Homologues of PhTX-12 with 7-11 methylene groups between the primary amino group and the aromatic head-group were synthesized using solid-phase methodology. In vitro electrophysiological studies of nAChR demonstrated that decreasing the number of methylene groups from 12 to 11 significantly increased potency. Antagonism by PhTX-11, like that of PhTX-12, was only weakly voltage-dependent. When the methylene spacer was reduced further, antagonism was decreased below that of PhTX-12, and in some cases potentiation of ACh responses by up to 60% was observed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromatography, High Pressure Liquid
  • Drug Evaluation, Preclinical
  • Mass Spectrometry
  • Nicotinic Antagonists / chemical synthesis*
  • Nicotinic Antagonists / chemistry
  • Nicotinic Antagonists / pharmacology*
  • Patch-Clamp Techniques
  • Polyamines*
  • Tyrosine / analogs & derivatives
  • Tyrosine / chemical synthesis*
  • Tyrosine / chemistry
  • Tyrosine / pharmacology*

Substances

  • Nicotinic Antagonists
  • Polyamines
  • phTX 12
  • Tyrosine