Antiplatelet aggregation principles from Glycosmis citrifolia

Twelve acridone alkaloids, citracridone‐I (1), atalaphyllidine (2), noracronycine (3), des‐N‐methylnoracronycine (4), 5‐hydroxynor‐acronycine (5), des‐N‐methylacronycine (6), N‐methyl severifoline (7), 5‐hydroxy‐N‐methyl severifoline (8), glycocitrine‐II (9), 3‐O‐methyl‐glycocitrine‐II (10), glycoci...

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Published inPTR. Phytotherapy research Vol. 12; no. S1; pp. S77 - S79
Main Authors Leu, Yann-Lii, Chan, Yu-Yi, Wu, Tian-Shung, Teng, Che-Ming, Chen, Kuo-Tung
Format Journal Article Conference Proceeding
LanguageEnglish
Published Chichester, UK John Wiley & Sons, Ltd 1998
Wiley
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Summary:Twelve acridone alkaloids, citracridone‐I (1), atalaphyllidine (2), noracronycine (3), des‐N‐methylnoracronycine (4), 5‐hydroxynor‐acronycine (5), des‐N‐methylacronycine (6), N‐methyl severifoline (7), 5‐hydroxy‐N‐methyl severifoline (8), glycocitrine‐II (9), 3‐O‐methyl‐glycocitrine‐II (10), glycocitrine‐I (11) and pyranofoline (12); one 2‐quinolone alkaloid, 4,8‐dimethoxy‐1‐methyl‐3(3‐methylbut‐2‐enyl)2‐quinolone (13) were isolated and characterized from the stem and root barks of Glycosmis citrifolia. Their structures were determined by spectral analyses. On bioactive evaluation, compounds 1 and 2 almost completely inhibited platelet aggregation induced by arachidonic acid (100 μM), collagen (10 μg/mL) and PAF (2 ng/mL). Compounds 2, 4 and 13 also showed an inhibitory effect on AA and collagen‐induced rabbit platelet aggregation. In the structure and activity relationship of acridone alkaloids, the acridone nucleus bearing a pyranyl moiety is a most important factor for the antiplatelet aggregation activity. © 1998 John Wiley & Sons, Ltd.
Bibliography:National Science Council, R.O.C.
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istex:709E7F5A0859F1A2951DE8616254A97EEB1771EA
ArticleID:PTR256
ISSN:0951-418X
1099-1573
DOI:10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-J