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Design of benzoxathiazin-3-one 1,1-dioxides as a new class of irreversible serine hydrolase inhibitors: discovery of a uniquely selective PNPLA4 inhibitor

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Its mechanism parallels GHK-Cu in theory, involving copper-mediated upregulation of growth factors near the dermal papilla, but the two compounds have not been compared head-to-head in peer-reviewed human studies

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