Synthesis and pharmacological evaluation of a novel AT1 angiotensin II receptor antagonist with anti-hypertension and anti-tumor effects

Clin Exp Hypertens. 2015;37(6):490-7. doi: 10.3109/10641963.2015.1013120. Epub 2015 Apr 28.

Abstract

A new compound 2-(4-((2-butyl-5-nitro-1H-benzo[d]imidazol-1-yl)methyl)-1H-indol-1-yl) benzamide (1) was designed, synthesized and evaluated as a novel AT1 receptor antagonist. Compound 1 displayed high affinity to AT1 receptor with an IC50 value of 1.65 ± 0.2 nM in radio-ligand binding assays. It had an efficient and long-lasting effect in reducing blood pressure which could last for more than 12 h at the dose of 10 mg/kg in spontaneously hypertensive rats. Acute toxicity tests suggested that compound 1 was safe with the LD50 value of 2519.81 mg/kg. Besides, in vitro and in vivo tests suggested its anti-proliferative and anti-tumor activities, respectively. So compound 1 could be considered as a novel anti-hypertension, anti-tumor candidate and deserved further investigation.

Keywords: Angiotensin II receptor antagonist; anti-hypertension; anti-tumor; hypertension; tumor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiotensin Receptor Antagonists / chemistry*
  • Angiotensin Receptor Antagonists / therapeutic use*
  • Animals
  • Benzamides / chemical synthesis*
  • Benzamides / therapeutic use*
  • Blood Pressure / drug effects*
  • Cell Line
  • Disease Models, Animal
  • Humans
  • Hypertension / drug therapy*
  • Hypertension / pathology
  • Hypertension / physiopathology
  • Male
  • Mice, Nude
  • Prostatic Neoplasms / drug therapy*
  • Prostatic Neoplasms / pathology
  • Rats
  • Rats, Inbred SHR

Substances

  • Angiotensin Receptor Antagonists
  • Benzamides
  • benzamide