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 in | PTR. Phytotherapy research Vol. 12; no. S1; pp. S77 - S79 |
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Main Authors | , , , , |
Format | Journal Article Conference Proceeding |
Language | English |
Published |
Chichester, UK
John Wiley & Sons, Ltd
1998
Wiley |
Subjects | |
Online Access | Get full text |
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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. |
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Bibliography: | National Science Council, R.O.C. ark:/67375/WNG-7PHNMHXW-R istex:709E7F5A0859F1A2951DE8616254A97EEB1771EA ArticleID:PTR256 |
ISSN: | 0951-418X 1099-1573 |
DOI: | 10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-J |