Synthesis and gastrointestinal pharmacology of a 3E,5Z diene analogue of misoprostol

J Med Chem. 1987 Jan;30(1):193-7. doi: 10.1021/jm00384a032.

Abstract

A stereospecific synthesis and the gastric antisecretory and diarrheal activity of a 3E,5Z diene analogue of misoprostol are described. The key intermediate in the synthesis was an alpha chain truncated acetylene that was obtained by a cuprate/enolate capture procedure on the corresponding cyclopentenone. Palladium-catalyzed coupling of the acetylene with methyl 4-iodo-3(E)-butenoate provided the conjugated enyne. Although selective hydrogenation of the enyne with Lindlar catalyst failed, the desired 3E,5Z diene was obtained with P-2 nickel as catalyst. The diene was about 3 times more potent than misoprostol in inhibiting gastric acid secretion in dogs and also in producing diarrhea in rats.

Publication types

  • Comparative Study

MeSH terms

  • Alprostadil / analogs & derivatives
  • Alprostadil / pharmacology
  • Animals
  • Arbaprostil / analogs & derivatives
  • Arbaprostil / chemical synthesis*
  • Arbaprostil / pharmacology
  • Arbaprostil / toxicity
  • Diarrhea / chemically induced
  • Dogs
  • Gastric Juice / drug effects
  • Gastric Juice / metabolism*
  • Indicators and Reagents
  • Magnetic Resonance Spectroscopy
  • Male
  • Misoprostol
  • Prostaglandins E, Synthetic / chemical synthesis*
  • Rats
  • Structure-Activity Relationship

Substances

  • Indicators and Reagents
  • Prostaglandins E, Synthetic
  • Misoprostol
  • 15-deoxy-16-methyl-16-hydroxy-3,4-didehydroprostaglandin E2 methyl ester
  • Alprostadil
  • Arbaprostil