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In vitro receptor binding assays demonstrated alchorneine's affinity for mu-opioid receptors with Ki values in the low micromolar range. Animal studies (hot-plate and writhing tests in mice) showed significant dose-dependent analgesic effects comparable to moderate doses of standard analgesics. A 2003 study in the Journal of Ethnopharmacology confirmed anti-nociceptive activity of the bark extract in multiple pain models.
Representative pattern: C₉H₇N₂O
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