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Pawhuskin A is a naturally-occurring prenylated stilbene isolated from ''Dalea purpurea'' which acts as a competitive silent antagonist of the κ-, μ-, and δ-opioid receptors (Ke = 203 nM, 570 nM, and 2900 nM, respectively). The compound was named after Pawhuska, Oklahoma, a place near where the samples of ''Dalea purpurea'' that led to its discovery were taken from.〔 Other isolates of the plant with affinity for opioid receptors include pawhuskin B and pawhuskin C, though these compounds produce comparatively weak opioid receptor displacement (4.2–11.4 μM) relative to pawhuskin A.〔〔 ''Dalea purpurea'' was used in traditional Native American medicine to treat various ailments, and pawhuskin A and related isolates may be some of the constituents of the plant which underlied this use.〔 ==See also== * Amentoflavone * Catechin * Hyperoside * Salvinorin A 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「Pawhuskin A」の詳細全文を読む スポンサード リンク
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