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Hypoxoside has been demonstrated to convert reliably to rooperol in vivo in human pharmacokinetic studies. Orally administered hypoxoside achieves measurable rooperol plasma levels within 1–2 hours. Standardisation of raw corm preparations to hypoxoside content (0.3–1.2% w/w dried corm) is feasible by HPLC. The prodrug approach avoids premature catechol oxidation that would render rooperol inactive before absorption.
Representative pattern: C₄H₂NO
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