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doi: 10.1002/jcp.30468 14 ZhangTXiQSWangDLiJJWangMLiDet al

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

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