Digoxin derivatives substituted by alkylidene at the butenolide part

Steroids. 2010 Jun;75(6):419-23. doi: 10.1016/j.steroids.2010.02.007. Epub 2010 Feb 18.

Abstract

A series of digoxin derivatives containing the gamma-alkylidene butenolide moiety were synthesised by way of stereoselective vinylogous aldol reaction of the unactivated butenolide in simple conditions. The structures of compounds synthesised were characterised by infrared (IR), nuclear magnetic resonance (NMR) and HR-MS. Preliminary bioassay shows that some of them have cardiac functions, especially compound 2g that induced a marked increase in myocardial contractility at 10ngml(-1) and 20ngml(-1) concentrations without digitalis toxicity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4-Butyrolactone / analogs & derivatives*
  • 4-Butyrolactone / chemical synthesis
  • 4-Butyrolactone / chemistry
  • 4-Butyrolactone / pharmacology
  • Animals
  • Biological Assay / methods
  • Digoxin* / analogs & derivatives
  • Digoxin* / chemical synthesis
  • Digoxin* / pharmacology
  • Guinea Pigs
  • Heart / drug effects
  • Humans
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Spectrophotometry, Infrared

Substances

  • Digoxin
  • butenolide
  • 4-Butyrolactone