Platelet aggregation inhibitor from Murraya euchrestifolia

Tian-Shung Wu, Yu Yi Chan, Meei Jen Liou, Ful Wen Lin, Li Shian Shi, Kuo Tung Chen

研究成果: Article同行評審

36 引文 斯高帕斯(Scopus)


Twenty-three carbazole alkaloids, murrayafoline-A (1), 3-methyl- carbazole (2), murrayanine (3), mukoeic acid (4), murrayazolidine (5), bicyclomahanimbine (6), murrayamine-A (10), -D (13), -E (14), -F (15), -I (16), -J (17), -K (18), -M (7), -N (19), murrayazoline (8), girinimbine (9), mahanimbine (11), (+)-mahanine (12), isomahanine (20), murrafoline-A (21), - B (22) and bismurrayafoline-A (23) and a triterpenoid, friedelin together with β-sitosterol were isolated and characterized from the leaves and root bark of M. euchrestifolia. Their structures were elucidated by spectroscopic analyses and/or direct comparison with authentic samples. The isolated carbazole alkaloids 1-12 were subjected to evaluation for antiplatelet aggregation activity and vasorelaxing effect. Most of the isolated carbazole alkaloids showed potent inhibitory, activity on rabbit platelet aggregation induced by arachidonic acid (100 μM), collagen (10 μg/mL) and PAF (2 ng/mL). Only murrayafoline-A (1) showed inhibition of tonic contraction induced by K+ (80 mM) + Ca2+ (1.9 mM). Compounds 1, 7 and 12 showed the promotion of the platelet aggregation or lysis at high dose. In contrast, they also exhibited antiplatelet aggregation activity at low concentration. This result could continue the philosophy of use in Chinese medicine, in that the dose variation in a prescription produced different, promotive or inhibitive, effects on therapy.

期刊Phytotherapy Research
發行號SUPPL. 1
出版狀態Published - 1998 一月 1

All Science Journal Classification (ASJC) codes

  • Pharmacology

指紋 深入研究「Platelet aggregation inhibitor from Murraya euchrestifolia」主題。共同形成了獨特的指紋。