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It is buried in the same orthosteric site of the ghrelin receptor and displays comparable potency for receptor activation (Fig

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This assay in the presence of hydrogen peroxide (H 2 O 2 ) and horseradish peroxidase (HRP) uses a substituted phenol (3,5-dichloro-2-hydroxybenzenesulfonic acid) that combines with 4-aminoantipyrine to form a red quinoneimine dye

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