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Description

A cell-permeable, more potent inhibitor of endothelial nitric oxide synthase (eNOS, IC50 = 500 nM) compared to other arginine analogs such as L-NAME (Cat. No. 483125) and L-NMMA (Cat. No. 475886). Inhibits acetylcholine-induced relaxation of rat aorta rings (IC50 = 2 µ,M) and causes a dose-dependent increase in mean arterial blood pressure in the rat (EC50 = 19.5 mg/kg)., Cell permeable. Approximately five times more potent as an inhibitor of endothelial nitric oxide synthase (IC50 = 500 nM) than other arginine analogs, such as L-NAME (Cat. No. 483125) and L-NMMA (Cat. No. 475886). Inhibits acetylcholine induced relaxation of rat aorta rings (IC50 = 2 µ,M) and causes a dose-dependent increase in mean arterial blood pressure in the rat (EC50 = 19.5 mg/kg).

Structure formula

N5-(1-Iminoethyl)-L-ornithine Dihydrochloride

Contents

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