Antihypertensive ergoline derivatives

Drug Des Deliv. 1987 May;1(4):313-23.

Abstract

Novel ergolines were synthesized and screened in spontaneous hypertensive rats (SHR) with the aim of finding a new class of ergot related antihypertensives. Their prolactin inhibitory effect (measured as nidation inhibition in rats), acute toxicity (LD50) and interference with CNS function (Irwin test) were also evaluated as a measure of selectivity and safety. Modification of the C8 side-chain enhanced antihypertensive activity selectively, while the introduction of substituents in other positions of the ergoline skeleton generally yielded unfavourable results, either by decreasing selectivity or by increasing toxicity.

MeSH terms

  • Animals
  • Antihypertensive Agents*
  • Blood Pressure / drug effects
  • Ergolines / chemical synthesis
  • Ergolines / pharmacology*
  • Ergolines / toxicity
  • Isoxazoles / chemical synthesis
  • Isoxazoles / pharmacology
  • Isoxazoles / toxicity
  • Male
  • Mice
  • Prolactin / antagonists & inhibitors
  • Pyrazoles / chemical synthesis
  • Pyrazoles / pharmacology
  • Pyrazoles / toxicity
  • Pyrimidines / chemical synthesis
  • Pyrimidines / pharmacology
  • Pyrimidines / toxicity
  • Rats
  • Rats, Inbred SHR
  • Rats, Inbred Strains
  • Structure-Activity Relationship

Substances

  • Antihypertensive Agents
  • Ergolines
  • Isoxazoles
  • Pyrazoles
  • Pyrimidines
  • Prolactin