DescriptionA potent and selective competitive antagonist for the angiotensin II type 1 (AT1) receptor. Displaces [125I]-angiotensin II binding with an IC50 value of 3.8 nM in guinea pig adrenal gland membranes. Orally active, and is more potent and longer-acting than the prototype AT1 antagonist, losartan.
|Observed MW: 474.99|
Safety and Handling
Recommended Storage : Desiccate at +4°C
For Research Use Only
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