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对恶唑基硫代丙酸衍生物EMD 26 644的血小板黏附及聚集抑制作用的人体药理学研究。

Human-pharmacological investigations on the platelet adhesiveness- and aggregation-inhibiting effect of EMD 26 644, an oxazolyl-thio-propionic acid derivate.

作者信息

Jacobi E, Leopold G, Lissner R, Maisenbacher J

出版信息

Int J Clin Pharmacol Biopharm. 1978 Mar;16(3):136-41.

PMID:649232
Abstract

EMD 26 644, a compound of novel chemical structure and with platelet aggregation-inhibiting properties, was investigated in 2 controlled clinical pharmacological studies involving 42 normal volunteers. In the first study with 22 subjects exhibiting normal or spontaneously increased platelet aggregation the influence of 1 X 250 mg EMD 26 644 p.o. on the platelet aggregation and adhesiveness was examined ex vivo. In the second study 20 subjects with and without a premedication of 1 X 250 mg EMD 26 644 were exposed an artificial climate with special platelet-irritating properties. A single oral dose of 250 mg EMD 26 644 markedly and significantly inhibited the platelet aggregation and adhesiveness over a period of several days.

摘要

EMD 26 644是一种具有新型化学结构且具有血小板聚集抑制特性的化合物,在两项涉及42名正常志愿者的对照临床药理学研究中进行了调查。在第一项研究中,22名血小板聚集正常或自发增加的受试者口服1×250 mg EMD 26 644,对血小板聚集和黏附性的影响进行了体外检测。在第二项研究中,20名服用或未服用1×250 mg EMD 26 644预处理药物的受试者暴露于具有特殊血小板刺激特性的人工气候环境中。单次口服250 mg EMD 26 644在数天内显著抑制了血小板聚集和黏附性。

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