Azilsartan-d4 is a deuterium-labeled analog of Azilsartan, a potent and selective antagonist of the angiotensin II type 1 receptor (AT1). This stable isotope plays a key role in tracing and quantifying the pharmacokinetics of Azilsartan in biological systems. Additionally, Azilsartan promotes reactive oxygen species (ROS) formation and apoptosis in HepG2 cancer cells, demonstrating potential neuroprotective and anticancer properties. It is applicable in research focused on hypertension and stroke mechanisms.
Azilsartan-d4 is a deuterium-labeled analog of Azilsartan, a potent and selective antagonist of the angiotensin II type 1 receptor (AT1). This stable isotope plays a key role in tracing and quantifying the pharmacokinetics of Azilsartan in biological systems. Additionally, Azilsartan promotes reactive oxygen species (ROS) formation and apoptosis in HepG2 cancer cells, demonstrating potential neuroprotective and anticancer properties. It is applicable in research focused on hypertension and stroke mechanisms.
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