In vitro pharmacological characterization of a new selective angiotensin AT1 receptor antagonist, UR-7280

Eur J Pharmacol. 1996 Dec 30;318(2-3):341-7. doi: 10.1016/s0014-2999(96)00794-7.

Abstract

UR-7280 (3-tert-butyl-1-propyl-5-[[2'-(1H-tetrazol-5-yl)-1,1'-biphenyl-4-y l]methyl]-1H-pyrazole-4-carboxylic acid) is a new and potent angiotensin AT1-selective receptor antagonist. Binding studies in rat liver membranes showed that UR-7280 is an apparently competitive antagonist. However, in rabbit aorta this compound antagonized the angiotensin II-induced contractile response in an insurmountable way, causing a significant reduction of the maximal response. Additional binding studies evidenced that UR-7280 has a slowly reversible binding profile, consistent with its functional properties in rabbit aorta. The results obtained with a series of structural analogues of UR-7280 demonstrated a relationship between the size of the pyrazole 3-substituent and the surmountable or insurmountable mode of antagonism, indicating that this position may play a key role in the interaction between the antagonist and the angiotensin AT1 receptor.

MeSH terms

  • Angiotensin II / antagonists & inhibitors
  • Angiotensin Receptor Antagonists*
  • Animals
  • In Vitro Techniques
  • Male
  • Muscle, Smooth, Vascular / drug effects
  • Muscle, Smooth, Vascular / physiology
  • Pyrazoles / pharmacology*
  • Rabbits
  • Rats
  • Structure-Activity Relationship
  • Tetrazoles / pharmacology*
  • Vasoconstriction / drug effects

Substances

  • Angiotensin Receptor Antagonists
  • Pyrazoles
  • Tetrazoles
  • UR 7280
  • Angiotensin II