Synthesis and pharmacological evaluation of carbamic acid 1-phenyl-3-(4-phenyl-piperazine-1-yl)-propyl ester derivatives as new analgesic agents

Bioorg Med Chem Lett. 2012 Apr 1;22(7):2434-9. doi: 10.1016/j.bmcl.2012.02.023. Epub 2012 Feb 16.

Abstract

A series of carbamic acid 1-phenyl-3-(4-phenyl-piperazine-1-yl)-propyl ester derivatives were synthesized through discovery strategies for balancing target-based in vitro screening and phenotypic in vivo screening. All the newly synthesized compounds were screened for their analgesic activities and compared with standard drug morphine. Among them, compound 44r, a potent analgesic agent that has favorable pharmacokinetic properties in rats and most importantly, has a wide safety margin. We demonstrated with in vitro and in vivo functional assays that its analgesic activity might be through 5-HT(2A) antagonism to some extent. Hence, it is concluded that there is ample scope for further study in developing compound 44r as a good lead candidate for an analgesic agent.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analgesics / chemical synthesis*
  • Analgesics / pharmacology
  • Animals
  • Carbamates / chemical synthesis*
  • Carbamates / pharmacology
  • Esters
  • Mice
  • Molecular Structure
  • Morphine / pharmacology
  • Pain / drug therapy*
  • Pain Measurement
  • Piperazines / chemical synthesis*
  • Piperazines / pharmacology
  • Rats
  • Receptors, Serotonin, 5-HT2 / metabolism
  • Serotonin Antagonists / chemical synthesis*
  • Serotonin Antagonists / pharmacology
  • Structure-Activity Relationship

Substances

  • Analgesics
  • Carbamates
  • Esters
  • Piperazines
  • Receptors, Serotonin, 5-HT2
  • Serotonin Antagonists
  • Morphine