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Replacing the C-terminal amide of the MT-II scaffold with a hydroxyl group yields a related cyclic peptide with a distinct receptor-selectivity profile, while retaining the lactam-bridged, enzymatically stable architecture
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These findings are in parallel with an earlier study reported in the preclinical study for resveratrol, largely present in red wine, in which it has chemopreventive effects against prostate cancer [96]
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