Influence of chain length and N-alkylation on the selective serotonin receptor ligand 9-(aminomethyl)-9,10-dihydroanthracene

Bioorg Med Chem Lett. 2001 Mar 12;11(5):655-8. doi: 10.1016/s0960-894x(01)00023-3.

Abstract

Comparison of the serotonin 5-HT2A receptor affinities of chain lengthened and N-alkylated analogues of the novel ligand 9-aminomethyl-9,10-dihydroanthracene (AMDA) and a structurally similar prototypical tricyclic amine imipramine suggests that the two agents bind to the receptor in different fashions. The demonstration that AMDA is highly selective for serotonin receptors (5-HT2A, K = 20nM; 5-HT2C, Ki=43nM) versus the dopamine D2 receptor (Ki>10,000nM), as well as the serotonin and norepinephrine transporters (Ki>10,000nM) further suggests that AMDA and the nonselective ligand imipramine interact with these target macromolecules in different ways.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Anthracenes / chemistry*
  • Anthracenes / metabolism
  • Cell Line
  • Ligands
  • Molecular Conformation
  • Molecular Structure
  • Radioligand Assay
  • Receptor, Serotonin, 5-HT2A
  • Receptors, Serotonin / metabolism*
  • Serotonin Antagonists / chemistry*
  • Serotonin Antagonists / metabolism

Substances

  • 9-(aminomethyl)-9,10-dihydroanthracene
  • Anthracenes
  • Ligands
  • Receptor, Serotonin, 5-HT2A
  • Receptors, Serotonin
  • Serotonin Antagonists