Synthesis and preliminary pharmacological assessment of novel 9-alkylamino substituted pyrimidino-[2,1-f]-purines

Pol J Pharmacol Pharm. 1992 Sep-Oct;44(5):487-503.

Abstract

Two series of N9-alkylaminomethyl-, alkylpiperazino-, alkylpiperidino-substituted 1,3-dimethyl-(hexahydropyrimidino)- and (tetrahydropyrimidono)-[2,1-f]-purines were prepared and their physicochemical and pharmacological properties were described. The most active in central nervous system tests were the compounds with phenylpiperazinealkyl substituent i.e. 1,3-dimethyl-2,4-dioxo-9-[N1N4-(phenyl)-piperazinopropyl]-1, 3,6,7,8,9- hexahydropyrimidino-[2,1-f] purine 6a and its butyl and isobutyl homologs 9 and 12. The compounds depressed statistically significantly spontaneous locomotor and amphetamine activity and showed sedative, analgetic and hypothermizing properties.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Behavior, Animal / drug effects*
  • Body Temperature / drug effects
  • Central Nervous System Depressants / chemical synthesis
  • Central Nervous System Depressants / pharmacology*
  • Central Nervous System Depressants / toxicity
  • Drug Evaluation, Preclinical
  • Magnetic Resonance Spectroscopy
  • Male
  • Mice
  • Motor Activity / drug effects
  • Purines / chemical synthesis
  • Purines / pharmacology*
  • Purines / toxicity
  • Rats
  • Rats, Wistar

Substances

  • Central Nervous System Depressants
  • Purines