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Phenolic and iridoid glycosides from Strychnos axillaris

Atsuko Itoh1, Yasuhiro Tanaka, Naotaka Nagakura

  • 1Kobe Pharmaceutical University, Higashinada-ku, Kobe 658-8558, Japan.

Phytochemistry
|February 6, 2008
PubMed

Abstract:

Five phenolic glycosides 1-5 and an iridoid glucoside 6 were isolated, together with 22 known compounds, from the dried barks and woods of Strychnosaxillaris. Their structures were determined by application of spectroscopic (NMR, MS) and chemical methodologies.

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Adrenergic agonists' structure-activity relationship (SAR) determines their selectivity and efficacy. These agonists comprise a phenylethylamine moiety with an aromatic ring and an ethylamine side chain.
Aromatic ring substitutions: Substituting the aromatic ring with –OH groups at positions 3 and 4 yields catecholamines (e.g., epinephrine), which have a high affinity for adrenoceptors. Hydrogen bonding between –OH groups and receptors enhances adrenergic activity.
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