腺苷酸激酶
环化酶
血小板
激活剂(遗传学)
凝血酶
血小板聚集
化学
生物化学
药理学
生物
酶
免疫学
受体
作者
Alain Beretz,Annick Roth-Georger,Gilles Corre,B. Kuballa,Robert Anton,Jean‐Pierre Cazenave
出处
期刊:Planta Medica
[Thieme Medical Publishers (Germany)]
日期:1985-08-01
卷期号:51 (04): 300-303
被引量:23
标识
DOI:10.1055/s-2007-969496
摘要
Quadrigemine B, quadrigemine A, isopsychotridine C and psychotridine, isolated from PSYCHOTRIA FORSTERIANA, are potent inhibitors of the aggregation of washed human platelets induced by ADP, collagen or thrombin. The four compounds are active in the 1-10 microM range. The quadrigemine-type alkaloids do not increase the level of platelet cyclic AMP, either alone or in the presence of 20 nM prostaglandin E, (PGE (1)), an activator of adenylate cyclase. The characteristics of the pharmacological action of these compounds suggest that they act at a later stage in platelet activation, possibly through an interaction with cytoskeletal proteins.
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