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2012 Jan;9(1):79

Dihexa-based compounds do not interact with central or peripheral AT 1 receptors, are highly target specific, exhibit little interaction with cardiac channel proteins and hepatic CIP isoforms, and reveal no acute toxicity following a 6x effective dose of Dihexa

The drug deferiprone has been shown to inhibit ferroptosis by chelating excess iron within the substantia nigra in vivo (52)

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