Synthesis and binding affinity of new pyrazole and isoxazole derivatives as potential atypical antipsychotics

Bioorg Med Chem Lett. 2007 Sep 1;17(17):4873-7. doi: 10.1016/j.bmcl.2007.06.045. Epub 2007 Jun 14.

Abstract

We describe the synthesis and binding affinities on D(2), 5-HT(2A) and 5-HT(2C) receptors of 6-aminomethyl-6,7-dihydro-1H-indazol-4(5H)-ones and 6-aminomethyl-6,7-dihydro-3-methyl-benzo[d]isoxazol-4(5H)-ones, as conformationally constrained butyrophenone analogues. One of the new compounds showed good in vitro binding features, and a Meltzer's ratio characteristic of an atypical antipsychotic profile.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antipsychotic Agents / chemical synthesis
  • Antipsychotic Agents / chemistry
  • Antipsychotic Agents / pharmacology*
  • Chemistry, Pharmaceutical / methods
  • Drug Design
  • Humans
  • Hydrogen Bonding
  • Isoxazoles / chemical synthesis
  • Isoxazoles / chemistry*
  • Kinetics
  • Models, Chemical
  • Molecular Conformation
  • Protein Binding
  • Pyrazoles / chemical synthesis
  • Pyrazoles / chemistry*
  • Receptor, Serotonin, 5-HT2A / chemistry
  • Receptor, Serotonin, 5-HT2C / chemistry
  • Receptors, Dopamine D2 / chemistry
  • Software

Substances

  • Antipsychotic Agents
  • Isoxazoles
  • Pyrazoles
  • Receptor, Serotonin, 5-HT2A
  • Receptor, Serotonin, 5-HT2C
  • Receptors, Dopamine D2