Terfenadine-d 3 ((±)-Terfenadine-d 3 ) is the deuterium labeled Terfenadine. Terfenadine ((±)-Terfenadine) is a potent open-channel blocker of hERG with an IC 50 of 204 nM. Terfenadine, an H1 histamine receptor antagonist , acts as a potent apoptosis inducer in melanoma cells through modulation of Ca2+ homeostasis. Terfenadine induces ROS-dependent apoptosis , simultaneously activates Caspase-4, -2, -9[2].
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