Synthesis and hypoglycemic activity of phenacyltriphenylphosphoranes and phosphonium salts

J Med Chem. 1975 Sep;18(9):952-4. doi: 10.1021/jm00243a021.

Abstract

Phenacyl-riphenylphosphorane (1a) and several analogs substituted in the meta position of the phenacyl group lowered blood glucose levels in 48-hr fasted rats. The corresponding phosphonium salts had comparable hypoglycemic activity. Two compounds (1a and 1b) were also hypoglycemic in fed rats, but hypoglycemia could not be elicited in another species.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Blood Glucose / analysis
  • Depression, Chemical
  • Hypoglycemic Agents / chemical synthesis*
  • Male
  • Onium Compounds / chemical synthesis
  • Onium Compounds / pharmacology
  • Phosphoranes / chemical synthesis*
  • Phosphoranes / pharmacology
  • Rats
  • Structure-Activity Relationship

Substances

  • Blood Glucose
  • Hypoglycemic Agents
  • Onium Compounds
  • Phosphoranes