Description
An AT2 receptor antagonist (IC50 = 1.2 nM in rat adrenal gland membranes); binds to the AT1 receptor (Ki = 46.6 nM in rat liver epithelial cells); reduces the AT2-induced pressor response in rats; decreases mean arterial pressure in a rat model of hypertension induced by renal artery constriction at 1 and 3 mg/kg intragastrically or intravenously
Formal name: 5,8-dihydro-2,4-dimethyl-8-[[2′-(2H-tetrazol-5-yl)[1,1′-biphenyl]-4-yl]methyl]-pyrido[2,3-d]pyrimidin-7(6H)-one
Synonyms: WAY-ANA-756
Molecular weight: 411.5
CAS: 145733-36-4
Purity: ≥98%
Formulation: A crystalline solid