[Research concerning rutin semisynthetic derivatives, synthesis and pharmaco-toxicological properties of some new morpholine and piperidine derivatives]

Rev Med Chir Soc Med Nat Iasi. 2003 Jan-Mar;107(1):192-6.
[Article in Romanian]

Abstract

In order to continue the research of the rutin semisynthetic derivatives we obtained some new morpholine and piperidine derivatives. Melting points, solubility, yield, C, H, N elemental analysis and UV spectra characterised all of these compounds. The toxicity was established by intraperitoneal administration at mice; the values of LD50 are between 743.75 and 856.25 mg/kg (medium toxicity). Pharmacological assays included the following parameters: leukocytes formula, NBT test, and serum complement activity. The new derivatives of rutin have a very good solubility in water, a pH closed to physiological value and immunosuppressive activity: peripheric blood PMN and lymphocytes are decreased; fagocytic capacity of peripheric blood PMN is also decreased; serum complement activity is not changed.

Publication types

  • English Abstract

MeSH terms

  • Animals
  • Calcium Channel Blockers / pharmacology*
  • Calcium Channel Blockers / toxicity
  • Injections, Intraperitoneal
  • Lymphocytes / drug effects
  • Mice
  • Models, Animal
  • Morpholines / pharmacology*
  • Morpholines / toxicity
  • Neutrophils / drug effects
  • Piperidines / pharmacology*
  • Piperidines / toxicity
  • Rats
  • Rats, Wistar
  • Rutin / pharmacology*
  • Rutin / toxicity

Substances

  • Calcium Channel Blockers
  • Morpholines
  • Piperidines
  • Rutin
  • piperidine
  • morpholine