Platelet antiaggregant methoxyphenylthienyl ketoxime ethers: synthesis and structure-activity relationships

Arch Pharm (Weinheim). 1995 May;328(5):417-24. doi: 10.1002/ardp.19953280505.

Abstract

Some new oximinoalkanoic (n = 2,3,4) esters and acids derived from methoxyphenylthienyl ketones have been synthesized and evaluated in vitro for their inhibitory effects on arachidonic acid-induced human platelet aggregation. Of the eighteen oximinoethers tested the most active derivatives, which were four times more active as aspirin, belonged to the para methoxy series with Z configuration and n = 2 or 3.

MeSH terms

  • Ethers / chemical synthesis*
  • Ethers / pharmacology
  • Humans
  • Hydrolysis
  • In Vitro Techniques
  • Magnetic Resonance Spectroscopy
  • Platelet Aggregation / drug effects
  • Platelet Aggregation Inhibitors / chemical synthesis*
  • Platelet Aggregation Inhibitors / pharmacology
  • Structure-Activity Relationship

Substances

  • Ethers
  • Platelet Aggregation Inhibitors