Synthesis and cholinesterase inhibitory activity of 6-, 7-methoxy-(and hydroxy-) tacrine derivatives

Farmaco. 1996 Nov;51(11):693-8.

Abstract

Some 6- and 7-methoxy-(and hydroxy-) tacrine derivatives were synthesized and evaluated for their in vitro acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) inhibitory activities. The most potent analogue in our series was the 9-heptylamino-6-methoxytacrine 3af which, in comparison with tacrine (THA), displayed an almost identical inhibitory effect, slightly lower acute toxicity and higher selectivity profile towards AchE when compared with THA.

MeSH terms

  • Animals
  • Cholinesterase Inhibitors / chemical synthesis*
  • Cholinesterase Inhibitors / pharmacology
  • Male
  • Mice
  • Rats
  • Rats, Sprague-Dawley
  • Structure-Activity Relationship
  • Tacrine / analogs & derivatives*

Substances

  • Cholinesterase Inhibitors
  • Tacrine