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Both peptides show published activity across rodent and cell-culture tissue-repair models without binding a single canonical receptor, distinguishing the blend from receptor-targeted compounds

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doi:10.1107/S0567740879011493

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methamphetamine) [70,152,153], dopamine receptor agonization (apomorphine) [70], dopamine receptor supersensitivity (haloperidol) [152] and reverse tolerance (amphetamine) [153]