Tasosartan is a long-acting angiotensin II (AngII) receptor antagonist.
性状
Solid
IC50 & Target[1][2]
Angiotensin II (AngII) receptor
体外研究(In Vitro)
Tasosartan is an orally active nonpeptide AngII antagonist that has demonstrates specific and selective AT1 receptor antagonistic activity in vitro. IC50 for inhibition of specific binding of I-AngII to rat adrenal membrane in the absence of proteins in binding buffer is 1.2±0.6 nM. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
Administration of Tasosartan at doses of 1.0 and 3.0 mg/kg (iv) significantly (p<0.05) attenuates the pressor response to angiotensin-II in rats. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;In solvent -80°C 6 months
参考文献
[1]. Maillard MP, et al. Tasosartan, enoltasosartan, and angiotensin II receptor blockade: the confounding role of protein binding. J Pharmacol Exp Ther. 2000 Nov;295(2):649-54.[2]. Elokdah HM, et al. Novel human metabolites of the angiotensin-II antagonist Tasosartan and their pharmacological effects. Bioorg Med Chem Lett. 2002 Aug 5;12(15):1967-71.
溶解度数据
In Vitro: DMSO : 125 mg/mL (303.80 mM; Need ultrasonic)配制储备液