Description
An α1-AR antagonist; inhibits binding of the α1-AR ligand, BE-2254, in rat hippocampus and liver, which highly express α1A- and α1B-ARs, respectively (IC50 = 1 nM for both); decreases norepinephrine-induced contraction of isolated guinea pig aorta at 1 nM
Formal name: [4-(4-amino-6,7-dimethoxy-2-quinazolinyl)-1-piperazinyl]bicyclo[2.2.2]octa-2,5-dien-2-yl-methanone
Synonyms: SZL-49
Molecular weight: 421.5
CAS: 107021-36-3
Purity: ≥95%
Formulation: A crystalline solid
Product Type|Biochemicals|Receptor Pharmacology||Research Area|Cardiovascular System|Vasculature|Vasodilation